| Year |
Citation |
Score |
| 2023 |
Ingannato A, Bessi V, Chiari A, Salvatori D, Bagnoli S, Bedin R, Ferrari C, Sorbi S, Nacmias B. GRN Missense Variants and Familial Alzheimer's Disease: Two Case Reports. Journal of Alzheimer's Disease : Jad. 96: 767-775. PMID 37899057 DOI: 10.3233/JAD-230689 |
0.328 |
|
| 2023 |
Mazzeo S, Lassi M, Padiglioni S, Vergani AA, Moschini V, Scarpino M, Giacomucci G, Burali R, Morinelli C, Fabbiani C, Galdo G, Amato LG, Bagnoli S, Emiliani F, Ingannato A, ... ... Sorbi S, et al. PRedicting the EVolution of SubjectIvE Cognitive Decline to Alzheimer's Disease With machine learning: the PREVIEW study protocol. Bmc Neurology. 23: 300. PMID 37573339 DOI: 10.1186/s12883-023-03347-8 |
0.31 |
|
| 2022 |
Ingannato A, Bagnoli S, Bessi V, Ferrari C, Mazzeo S, Sorbi S, Nacmias B. Intermediate alleles of HTT: A new pathway in longevity. Journal of the Neurological Sciences. 438: 120274. PMID 35580427 DOI: 10.1016/j.jns.2022.120274 |
0.306 |
|
| 2022 |
Bellenguez C, Küçükali F, Jansen IE, Kleineidam L, Moreno-Grau S, Amin N, Naj AC, Campos-Martin R, Grenier-Boley B, Andrade V, Holmans PA, Boland A, Damotte V, van der Lee SJ, Costa MR, ... ... Sorbi S, et al. New insights into the genetic etiology of Alzheimer's disease and related dementias. Nature Genetics. PMID 35379992 DOI: 10.1038/s41588-022-01024-z |
0.327 |
|
| 2020 |
Mazzeo S, Polito C, Padiglioni S, Berti V, Bagnoli S, Lombardi G, Piaceri I, Carraro M, Cristofaro MTD, Phy AP, Ferrari C, Nacmias B, Sorbi S, Bessi V. Linguistic profiles, brain metabolic patterns and rates of amyloid-β biomarker positivity in patients with mixed primary progressive aphasia. Neurobiology of Aging. PMID 33010672 DOI: 10.1016/J.Neurobiolaging.2020.09.004 |
0.343 |
|
| 2020 |
Rosas I, Martínez C, Coto E, Clarimón J, Lleó A, Illán-Gala I, Dols-Icardo O, Borroni B, Almeida MR, van der Zee J, Van Broeckhoven C, Bruni AC, Anfossi M, Bernardi L, ... ... Sorbi S, et al. Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia. Neurobiology of Aging. PMID 32972771 DOI: 10.1016/J.Neurobiolaging.2020.08.018 |
0.415 |
|
| 2020 |
Bessi V, Giacomucci G, Mazzeo S, Bagnoli S, Padiglioni S, Balestrini J, Tomaiuolo G, Piaceri I, Carraro M, Bracco L, Sorbi S, Nacmias B. PER2 C111G polymorphism, cognitive reserve and cognition in subjective cognitive decline and mild cognitive impairment. A 10-year follow-up study. European Journal of Neurology. PMID 32896064 DOI: 10.1111/Ene.14518 |
0.373 |
|
| 2020 |
Tavares TP, Mitchell DGV, Coleman KK, Coleman BL, Shoesmith CL, Butler CR, Santana I, Danek A, Gerhard A, de Mendonca A, Borroni B, Tartaglia MC, Graff C, Galimberti D, Tagliavini F, ... ... Sorbi S, et al. Early symptoms in symptomatic and preclinical genetic frontotemporal lobar degeneration. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 32769115 DOI: 10.1136/Jnnp-2020-322987 |
0.345 |
|
| 2020 |
Lombardi G, Pupi A, Bessi V, Polito C, Padiglioni S, Ferrari C, Lucidi G, Berti V, Cristofaro MTD, Piaceri I, Bagnoli S, Nacmias B, Sorbi S. Challenges in Alzheimer's Disease Diagnostic Work-Up: Amyloid Biomarker Incongruences. Journal of Alzheimer's Disease. 77: 203-217. PMID 32716357 DOI: 10.3233/Jad-200119 |
0.34 |
|
| 2020 |
Pomeshchik Y, Klementieva O, Gil J, Martinsson I, Hansen MG, de Vries T, Sancho-Balsells A, Russ K, Savchenko E, Collin A, Vaz AR, Bagnoli S, Nacmias B, Rampon C, Sorbi S, et al. Human iPSC-Derived Hippocampal Spheroids: An Innovative Tool for Stratifying Alzheimer Disease Patient-Specific Cellular Phenotypes and Developing Therapies. Stem Cell Reports. PMID 32589876 DOI: 10.1016/J.Stemcr.2020.06.001 |
0.391 |
|
| 2020 |
Bellinvia A, Pastò L, Niccolai C, Tessa A, Carrai R, Martinelli C, Moretti M, Amato MP, Santorelli FM, Sorbi S, Matà S. A new paraplegin mutation in a patient with primary progressive multiple sclerosis. Multiple Sclerosis and Related Disorders. 44: 102302. PMID 32570181 DOI: 10.1016/J.Msard.2020.102302 |
0.351 |
|
| 2020 |
Bessi V, Balestrini J, Bagnoli S, Mazzeo S, Giacomucci G, Padiglioni S, Piaceri I, Carraro M, Ferrari C, Bracco L, Sorbi S, Nacmias B. Influence of ApoE Genotype and Clock T3111C Interaction with Cardiovascular Risk Factors on the Progression to Alzheimer's Disease in Subjective Cognitive Decline and Mild Cognitive Impairment Patients. Journal of Personalized Medicine. 10: 45. PMID 32485802 DOI: 10.3390/Jpm10020045 |
0.407 |
|
| 2020 |
Piaceri I, Chiari A, Galli C, Bagnoli S, Ferrari C, Saavedra ST, Molinari MA, Vinceti G, Sorbi S, Nacmias B. Incomplete penetrance in familial Alzheimer's disease with PSEN1 Ala260Gly mutation Neurological Sciences. 41: 2263-2266. PMID 32328830 DOI: 10.1007/S10072-020-04421-6 |
0.396 |
|
| 2020 |
Mazzeo S, Padiglioni S, Bagnoli S, Carraro M, Piaceri I, Bracco L, Nacmias B, Sorbi S, Bessi V. Assessing the effectiveness of SCD-plus criteria in predicting the progression to Alzheimer's Disease: A 11-year follow-up study. European Journal of Neurology. 27: 894-899. PMID 32043740 DOI: 10.1111/Ene.14167 |
0.403 |
|
| 2020 |
Bessi V, Mazzeo S, Bagnoli S, Padiglioni S, Carraro M, Piaceri I, Bracco L, Sorbi S, Nacmias B. The implication of BDNF Val66Met polymorphism in progression from subjective cognitive decline to mild cognitive impairment and Alzheimer's disease: a 9-year follow-up study. European Archives of Psychiatry and Clinical Neuroscience. 270: 471-482. PMID 31560105 DOI: 10.1007/S00406-019-01069-Y |
0.409 |
|
| 2019 |
Sudre CH, Bocchetta M, Heller C, Convery R, Neason M, Moore KM, Cash DM, Thomas DL, Woollacott IOC, Foiani M, Heslegrave A, Shafei R, Greaves C, van Swieten J, Moreno F, ... ... Sorbi S, et al. White matter hyperintensities in progranulin-associated frontotemporal dementia: A longitudinal GENFI study. Neuroimage. Clinical. 24: 102077. PMID 31835286 DOI: 10.1016/J.Nicl.2019.102077 |
0.38 |
|
| 2019 |
Moore KM, Nicholas J, Grossman M, McMillan CT, Irwin DJ, Massimo L, Van Deerlin VM, Warren JD, Fox NC, Rossor MN, Mead S, Bocchetta M, Boeve BF, Knopman DS, Graff-Radford NR, ... ... Sorbi S, et al. Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study. The Lancet. Neurology. PMID 31810826 DOI: 10.1016/S1474-4422(19)30394-1 |
0.37 |
|
| 2019 |
Rosas I, Martínez C, Clarimón J, Lleó A, Illán-Gala I, Dols-Icardo O, Borroni B, Almeida MR, van der Zee J, Van Broeckhoven C, Bruni AC, Anfossi M, Bernardi L, Maletta R, Serpente M, ... ... Sorbi S, et al. Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease. Neurobiology of Aging. PMID 31810584 DOI: 10.1016/J.Neurobiolaging.2019.10.017 |
0.444 |
|
| 2019 |
Ferrari C, Polito C, Berti V, Lombardi G, Lucidi G, Bessi V, Bagnoli S, Piaceri I, Nacmias B, Sorbi S. High Frequency of Crossed Aphasia in Dextral in an Italian Cohort of Patients with Logopenic Primary Progressive Aphasia. Journal of Alzheimer's Disease. 72: 1089-1096. PMID 31683481 DOI: 10.3233/Jad-190677 |
0.301 |
|
| 2019 |
Tavares TP, Mitchell DGV, Coleman K, Shoesmith C, Bartha R, Cash DM, Moore KM, van Swieten J, Borroni B, Galimberti D, Tartaglia MC, Rowe J, Graff C, Tagliavini F, Frisoni G, ... ... Sorbi S, et al. Ventricular volume expansion in presymptomatic genetic frontotemporal dementia. Neurology. PMID 31578297 DOI: 10.1212/Wnl.0000000000008386 |
0.335 |
|
| 2019 |
Gazzina S, Grassi M, Premi E, Cosseddu M, Alberici A, Archetti S, Gasparotti R, Van Swieten J, Galimberti D, Sanchez-Valle R, Laforce RJ, Moreno F, Synofzik M, Graff C, Masellis M, ... ... Sorbi S, et al. Education modulates brain maintenance in presymptomatic frontotemporal dementia. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 31182509 DOI: 10.1136/Jnnp-2019-320439 |
0.314 |
|
| 2019 |
Mazzon G, Ajčević M, Cattaruzza T, Menichelli A, Guerriero M, Capitanio S, Pesavento V, Dore F, Sorbi S, Manganotti P, Marini A. Connected Speech Deficit as an Early Hallmark of CSF-defined Alzheimer's Disease and Correlation with Cerebral Hypoperfusion Pattern. Current Alzheimer Research. PMID 31057108 DOI: 10.2174/1567205016666190506141733 |
0.394 |
|
| 2019 |
Mazzeo S, Bessi V, Padiglioni S, Bagnoli S, Bracco L, Sorbi S, Nacmias B. KIBRA T allele influences memory performance and progression of cognitive decline: a 7-year follow-up study in subjective cognitive decline and mild cognitive impairment. Neurological Sciences. 40: 1559-1566. PMID 30953258 DOI: 10.1007/S10072-019-03866-8 |
0.348 |
|
| 2019 |
Mutsaerts HJMM, Mirza SS, Petr J, Thomas DL, Cash DM, Bocchetta M, de Vita E, Metcalfe AWS, Shirzadi Z, Robertson AD, Tartaglia MC, Mitchell SB, Black SE, Freedman M, Tang-Wai D, ... ... Sorbi S, et al. Cerebral perfusion changes in presymptomatic genetic frontotemporal dementia: a GENFI study. Brain : a Journal of Neurology. PMID 30847466 DOI: 10.1093/Brain/Awz039 |
0.343 |
|
| 2019 |
Rittman T, Borchert R, Jones S, van Swieten J, Borroni B, Galimberti D, Masellis M, Tartaglia MC, Graff C, Tagliavini F, Frisoni GB, Laforce R, Finger E, Mendonça A, Sorbi S, et al. Functional network resilience to pathology in presymptomatic genetic frontotemporal dementia. Neurobiology of Aging. 77: 169-177. PMID 30831384 DOI: 10.1016/J.Neurobiolaging.2018.12.009 |
0.325 |
|
| 2019 |
Premi E, Calhoun VD, Diano M, Gazzina S, Cosseddu M, Alberici A, Archetti S, Paternicò D, Gasparotti R, van Swieten J, Galimberti D, Sanchez-Valle R, Laforce R, Moreno F, Synofzik M, ... ... Sorbi S, et al. The inner fluctuations of the brain in presymptomatic Frontotemporal Dementia: The chronnectome fingerprint. Neuroimage. PMID 30716457 DOI: 10.1016/J.Neuroimage.2019.01.080 |
0.338 |
|
| 2019 |
Dalmasso MC, Brusco LI, Olivar N, Muchnik C, Hanses C, Milz E, Becker J, Heilmann-Heimbach S, Hoffmann P, Prestia FA, Galeano P, Avalos MSS, Martinez LE, Carulla ME, Azurmendi PJ, ... ... Sorbi S, et al. Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer's disease. Translational Psychiatry. 9: 55. PMID 30705288 DOI: 10.1038/S41398-019-0394-9 |
0.39 |
|
| 2019 |
Ferrari C, Polito C, Vannucchi S, Piaceri I, Bagnoli S, Lombardi G, Lucidi G, Berti V, Nacmias B, Sorbi S. Primary Progressive Aphasia: Natural History in an Italian Cohort. Alzheimer Disease & Associated Disorders. 33: 42-46. PMID 30640256 DOI: 10.1097/Wad.0000000000000282 |
0.387 |
|
| 2019 |
Mazzeo S, Padiglioni S, Bagnoli S, Bracco L, Nacmias B, Sorbi S, Bessi V. The dual role of cognitive reserve in subjective cognitive decline and mild cognitive impairment: a 7-year follow-up study. Journal of Neurology. 266: 487-497. PMID 30604054 DOI: 10.1007/S00415-018-9164-5 |
0.346 |
|
| 2019 |
Lucidi G, Berti V, Piaceri I, Ginestroni A, Lombardi G, Ferrari C, Polito C, Bessi V, Pupi A, Nacmias B, Sorbi S, Bagnoli S. Clinical and neuroimaging profiles to identify C9orf72‐FTD patients and serum Neurofilament to monitor the progression and the severity of the disease Neurology and Clinical Neuroscience. 7: 326-333. DOI: 10.1111/Ncn3.12331 |
0.33 |
|
| 2018 |
Cury C, Durrleman S, Cash DM, Lorenzi M, Nicholas JM, Bocchetta M, van Swieten JC, Borroni B, Galimberti D, Masellis M, Tartaglia MC, Rowe JB, Graff C, Tagliavini F, Frisoni GB, ... ... Sorbi S, et al. Spatiotemporal analysis for detection of pre-symptomatic shape changes in neurodegenerative diseases: Initial application to the GENFI cohort. Neuroimage. 188: 282-290. PMID 30529631 DOI: 10.1016/J.Neuroimage.2018.11.063 |
0.387 |
|
| 2018 |
Lombardi G, Polito C, Berti V, Bagnoli S, Nacmias B, Pupi A, Sorbi S. Contribution of Bilingualism to Cognitive Reserve of an Italian Literature Professor at High Risk for Alzheimer’s Disease Journal of Alzheimer's Disease. 66: 1389-1395. PMID 30475769 DOI: 10.3233/Jad-180736 |
0.364 |
|
| 2018 |
Young AL, Marinescu RV, Oxtoby NP, Bocchetta M, Yong K, Firth NC, Cash DM, Thomas DL, Dick KM, Cardoso J, van Swieten J, Borroni B, Galimberti D, Masellis M, Tartaglia MC, ... ... Sorbi S, et al. Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference. Nature Communications. 9: 4273. PMID 30323170 DOI: 10.1038/S41467-018-05892-0 |
0.387 |
|
| 2018 |
Zhang M, Ferrari R, Tartaglia MC, Keith J, Surace EI, Wolf U, Sato C, Grinberg M, Liang Y, Xi Z, Dupont K, McGoldrick P, Weichert A, McKeever PM, Schneider R, ... ... Sorbi S, et al. A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers. Brain : a Journal of Neurology. PMID 30252044 DOI: 10.1093/Brain/Awy238 |
0.376 |
|
| 2018 |
Jiskoot LC, Bocchetta M, Nicholas JM, Cash DM, Thomas D, Modat M, Ourselin S, Rombouts SARB, Dopper EGP, Meeter LH, Panman JL, van Minkelen R, van der Ende EL, Donker Kaat L, Pijnenburg YAL, ... ... Sorbi S, et al. Presymptomatic white matter integrity loss in familial frontotemporal dementia in the GENFI cohort: A cross-sectional diffusion tensor imaging study. Annals of Clinical and Translational Neurology. 5: 1025-1036. PMID 30250860 DOI: 10.1002/Acn3.601 |
0.305 |
|
| 2018 |
Colombo D, Caltagirone C, Padovani A, Sorbi S, Spalletta G, Simoni L, Ori A, Zagni E. Gender Differences in Neuropsychiatric Symptoms in Mild to Moderate Alzheimer's Disease Patients Undergoing Switch of Cholinesterase Inhibitors: A Post Hoc Analysis of the EVOLUTION Study. Journal of Women's Health (2002). 27: 1368-1377. PMID 30085899 DOI: 10.1089/Jwh.2017.6420 |
0.402 |
|
| 2018 |
Sellami L, Bocchetta M, Masellis M, Cash DM, Dick KM, van Swieten J, Borroni B, Galimberti D, Tartaglia MC, Rowe JB, Graff C, Tagliavini F, Frisoni G, Finger E, de Mendonça A, ... Sorbi S, et al. Distinct Neuroanatomical Correlates of Neuropsychiatric Symptoms in the Three Main Forms of Genetic Frontotemporal Dementia in the GENFI Cohort. Journal of Alzheimer's Disease : Jad. PMID 30010122 DOI: 10.3233/Jad-180053 |
0.36 |
|
| 2018 |
Baradaran-Heravi Y, Dillen L, Nguyen HP, Van Mossevelde S, Baets J, De Jonghe P, Engelborghs S, De Deyn PP, Vandenbulcke M, Vandenberghe R, Van Damme P, Cras P, Salmon E, Synofzik M, Heutink P, ... ... Sorbi S, et al. No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients. Neurobiology of Aging. PMID 29886022 DOI: 10.1016/J.Neurobiolaging.2018.05.005 |
0.361 |
|
| 2018 |
Fumagalli GG, Basilico P, Arighi A, Bocchetta M, Dick KM, Cash DM, Harding S, Mercurio M, Fenoglio C, Pietroboni AM, Ghezzi L, van Swieten J, Borroni B, de Mendonça A, Masellis M, ... ... Sorbi S, et al. Distinct patterns of brain atrophy in Genetic Frontotemporal Dementia Initiative (GENFI) cohort revealed by visual rating scales. Alzheimer's Research & Therapy. 10: 46. PMID 29793546 DOI: 10.1186/S13195-018-0376-9 |
0.341 |
|
| 2018 |
Bessi V, Mazzeo S, Padiglioni S, Piccini C, Nacmias B, Sorbi S, Bracco L. From Subjective Cognitive Decline to Alzheimer’s Disease: The Predictive Role of Neuropsychological Assessment, Personality Traits, and Cognitive Reserve. A 7-Year Follow-Up Study Journal of Alzheimer's Disease. 63: 1523-1535. PMID 29782316 DOI: 10.3233/Jad-171180 |
0.375 |
|
| 2018 |
Pottier C, Zhou X, Perkerson RB, Baker M, Jenkins GD, Serie DJ, Ghidoni R, Benussi L, Binetti G, López de Munain A, Zulaica M, Moreno F, Le Ber I, Pasquier F, Hannequin D, ... ... Sorbi S, et al. Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. The Lancet. Neurology. PMID 29724592 DOI: 10.1016/S1474-4422(18)30126-1 |
0.378 |
|
| 2018 |
Lombardi G, Polito C, Berti V, Ferrari C, Lucidi G, Bagnoli S, Piaceri I, Nacmias B, Pupi A, Sorbi S. Biomarkers study in atypical dementia: proof of a diagnostic work-up. Neurological Sciences. 39: 1203-1210. PMID 29651720 DOI: 10.1007/S10072-018-3400-8 |
0.356 |
|
| 2018 |
Piaceri I, Imperiale D, Ghidoni E, Atzori C, Bagnoli S, Ferrari C, Ungari S, Ambrogio L, Sorbi S, Nacmias B. Novel GRN Mutations in Alzheimer's Disease and Frontotemporal Lobar Degeneration Journal of Alzheimer's Disease. 62: 1683-1689. PMID 29614680 DOI: 10.3233/Jad-170989 |
0.424 |
|
| 2018 |
Philtjens S, Van Mossevelde S, van der Zee J, Wauters E, Dillen L, Vandenbulcke M, Vandenberghe R, Ivanoiu A, Sieben A, Willems C, Benussi L, Ghidoni R, Binetti G, Borroni B, Padovani A, ... ... Sorbi S, et al. Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia. Neurobiology of Aging. PMID 29555433 DOI: 10.1016/J.Neurobiolaging.2018.02.011 |
0.383 |
|
| 2018 |
Ferrari C, Nacmias B, Sorbi S. The diagnosis of dementias: a practical tool not to miss rare causes. Neurological Sciences. 39: 615-627. PMID 29198043 DOI: 10.1007/S10072-017-3206-0 |
0.391 |
|
| 2018 |
Terenzi F, Ferrari C, Bartolozzi C, Rotella F, Ghelli E, Mascherini E, Volpi E, Latorraca S, Bagnoli S, Nacmias B, Piacentini S, Sorbi S. G02 Decision-making in predictive testing in huntington’s disease Journal of Neurology, Neurosurgery, and Psychiatry. 89. DOI: 10.1136/Jnnp-2018-Ehdn.176 |
0.313 |
|
| 2017 |
Ferrari C, Lombardi G, Polito C, Lucidi G, Bagnoli S, Piaceri I, Nacmias B, Berti V, Rizzuto D, Fratiglioni L, Sorbi S. Alzheimer's Disease Progression: Factors Influencing Cognitive Decline. Journal of Alzheimer's Disease. 61: 785-791. PMID 29226870 DOI: 10.3233/Jad-170665 |
0.45 |
|
| 2017 |
Cash DM, Bocchetta M, Thomas DL, Dick KM, van Swieten JC, Borroni B, Galimberti D, Masellis M, Tartaglia MC, Rowe JB, Graff C, Tagliavini F, Frisoni GB, Laforce R, Finger E, ... ... Sorbi S, et al. Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI study. Neurobiology of Aging. 62: 191-196. PMID 29172163 DOI: 10.1016/J.Neurobiolaging.2017.10.008 |
0.352 |
|
| 2017 |
Piaceri I, Bessi V, Matà S, Polito C, Tedde A, Berti V, Bagnoli S, Braccia A, Mastio MD, Pignone AM, Pupi A, Sorbi S, Nacmias B. Association of the New Variant Tyr424Asp at TBK1 Gene with Amyotrophic Lateral Sclerosis and Cognitive Decline. Journal of Alzheimer's Disease. 61: 41-46. PMID 29103041 DOI: 10.3233/Jad-170694 |
0.359 |
|
| 2017 |
Nacmias B, Bagnoli S, Piaceri I, Sorbi S. Genetic Heterogeneity of Alzheimer's Disease: Embracing Research Partnerships. Journal of Alzheimer's Disease. 62: 903-911. PMID 29103034 DOI: 10.3233/Jad-170570 |
0.403 |
|
| 2017 |
Sims R, van der Lee SJ, Naj AC, Bellenguez C, Badarinarayan N, Jakobsdottir J, Kunkle BW, Boland A, Raybould R, Bis JC, Martin ER, Grenier-Boley B, Heilmann-Heimbach S, Chouraki V, Kuzma AB, ... ... Sorbi S, et al. Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nature Genetics. PMID 28714976 DOI: 10.1038/Ng.3916 |
0.392 |
|
| 2017 |
Gallo M, Frangipane F, Cupidi C, De Bartolo M, Turone S, Ferrari C, Nacmias B, Grimaldi G, Laganà V, Colao R, Bernardi L, Anfossi M, Conidi ME, Vasso F, Curcio SAM, ... ... Sorbi S, et al. The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family. Neurobiology of Aging. 56: 213.e7-213.e12. PMID 28532646 DOI: 10.1016/J.Neurobiolaging.2017.04.017 |
0.433 |
|
| 2017 |
Sudre CH, Bocchetta M, Cash D, Thomas DL, Woollacott I, Dick KM, van Swieten J, Borroni B, Galimberti D, Masellis M, Tartaglia MC, Rowe JB, Graff C, Tagliavini F, Frisoni G, ... ... Sorbi S, et al. White matter hyperintensities are seen only in GRN mutation carriers in the GENFI cohort. Neuroimage. Clinical. 15: 171-180. PMID 28529873 DOI: 10.1016/J.Nicl.2017.04.015 |
0.346 |
|
| 2017 |
Premi E, Grassi M, van Swieten J, Galimberti D, Graff C, Masellis M, Tartaglia C, Tagliavini F, Rowe JB, Laforce R, Finger E, Frisoni GB, de Mendonça A, Sorbi S, Gazzina S, et al. Cognitive reserve and TMEM106B genotype modulate brain damage in presymptomatic frontotemporal dementia: a GENFI study. Brain : a Journal of Neurology. PMID 28460069 DOI: 10.1093/Brain/Awx103 |
0.398 |
|
| 2017 |
De Roeck A, Van den Bossche T, van der Zee J, Verheijen J, De Coster W, Van Dongen J, Dillen L, Baradaran-Heravi Y, Heeman B, Sanchez-Valle R, Lladó A, Nacmias B, Sorbi S, Gelpi E, Grau-Rivera O, et al. Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease. Acta Neuropathologica. PMID 28447221 DOI: 10.1007/S00401-017-1714-X |
0.386 |
|
| 2017 |
Lombardi G, Berti V, Tedde A, Bagnoli S, Piaceri I, Polito C, Lucidi G, Ferrari C, Ginestroni A, Moretti M, Pupi A, Nacmias B, Sorbi S. Low Florbetapir PET Uptake and Normal Aβ1-42 Cerebrospinal Fluid in an APP Ala713Thr Mutation Carrier. Journal of Alzheimer's Disease. 57: 697-703. PMID 28304299 DOI: 10.3233/Jad-161170 |
0.373 |
|
| 2017 |
Jiskoot LC, Bocchetta M, Papma JM, Nicholas JM, Cash DM, Modat M, Borroni B, Galimberti D, Masellis M, Tartaglia MC, Rowe JB, Graff C, Tagliavini F, Frisoni GB, Laforce R, ... ... Sorbi S, et al. Presymptomatic White Matter Integrity Loss In Familial Frontotemporal Dementia In The Genetic Frontotemporal Dementia Initiative (Genfi) Cohort: A Multi-Centre, Cross-Sectional, Diffusion Tensor Imaging Study Alzheimers & Dementia. 13. DOI: 10.1016/J.Jalz.2017.06.453 |
0.313 |
|
| 2017 |
Sudre CH, Bocchetta M, Cash DM, Thomas DL, Woollacott IO, Dick KM, Swieten JCv, Borroni B, Galimberti D, Masellis M, Tartaglia MC, Rowe JB, Graff C, Tagliavini F, Frisoni GB, ... ... Sorbi S, et al. White Matter Hyperintensities In Genetic Frontotemporal Dementia: A Genfi Study Alzheimers & Dementia. 13. DOI: 10.1016/J.Jalz.2017.06.2634 |
0.325 |
|
| 2017 |
Young AL, Marinescu RV, Oxtoby NP, Bocchetta M, Cash DM, Thomas DL, Dick KM, Cardoso MJ, Ourselin S, Swieten JCv, Borroni B, Galimberti D, Masellis M, Tartaglia MC, Rowe JB, ... ... Sorbi S, et al. Multiple Distinct Atrophy Patterns Found In Genetic Frontotemporal Dementia Using Subtype And Stage Inference (Sustain) Alzheimers & Dementia. 13. DOI: 10.1016/J.Jalz.2017.06.2352 |
0.314 |
|
| 2017 |
Dick KM, Swieten JCv, Gerhard A, Ber IL, Frisoni GB, Dickerson BC, Graff C, Ghoshal N, Borroni B, Galimberti D, Mackenzie IR, Synofzik M, Sanchez-Valle R, Santana I, Moreno F, ... ... Sorbi S, et al. Symptom Onset In Genetic Frontotemporal Dementia Alzheimers & Dementia. 13: 1337. DOI: 10.1016/J.Jalz.2017.06.2056 |
0.314 |
|
| 2016 |
Bruti G, Cavallucci E, Mancini M, Bitossi A, Baldereschi M, Sorbi S. A systematic review of the quality of studies on dementia prevalence in Italy. Bmc Health Services Research. 16: 507. PMID 27659233 DOI: 10.1186/S12913-016-1741-7 |
0.376 |
|
| 2016 |
Castellini G, Lelli L, Tedde A, Piaceri I, Bagnoli S, Lucenteforte E, Sorbi S, Monteleone AM, James HJ, Nacmias B, Ricca V. Analyses of the role of the glucocorticoid receptor gene polymorphism (rs41423247) as a potential moderator in the association between childhood overweight, psychopathology, and clinical outcomes in Eating Disorders patients: A 6 years follow up study. Psychiatry Research. 243: 156-160. PMID 27400218 DOI: 10.1016/J.Psychres.2016.06.033 |
0.317 |
|
| 2016 |
Bocchetta M, Mega A, Bernardi L, Di Maria E, Benussi L, Binetti G, Borroni B, Colao R, Di Fede G, Fostinelli S, Galimberti D, Gennarelli M, Ghidoni R, Piaceri I, Pievani M, ... ... Sorbi S, et al. Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol. Journal of Alzheimer's Disease : Jad. 51: 277-91. PMID 26901402 DOI: 10.3233/Jad-150849 |
0.38 |
|
| 2016 |
Oldoni E, Fumagalli GG, Serpente M, Fenoglio C, Scarioni M, Arighi A, Bruno G, Talarico G, Confaloni A, Piscopo P, Nacmias B, Sorbi S, Rainero I, Rubino E, Pinessi L, et al. PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population. Journal of Alzheimer's Disease : Jad. PMID 26757195 DOI: 10.3233/Jad-150863 |
0.417 |
|
| 2016 |
Berti V, Polito C, Lombardi G, Ferrari C, Sorbi S, Pupi A. Rethinking on the concept of biomarkers in preclinical Alzheimer’s disease Neurological Sciences. 1-10. DOI: 10.1007/S10072-016-2477-1 |
0.389 |
|
| 2015 |
Tedde A, Bartoli A, Piaceri I, Ferrara S, Bagnoli S, Serio A, Sorbi S, Nacmias B. Novel presenilin 1 mutation (Ile408Thr) in an Italian family with late-onset Alzheimer's disease. Neuroscience Letters. 610: 150-153. PMID 26549787 DOI: 10.1016/J.Neulet.2015.11.004 |
0.431 |
|
| 2015 |
Cacace R, Van den Bossche T, Engelborghs S, Geerts N, Laureys A, Dillen L, Graff C, Thonberg H, Chiang HH, Pastor P, Ortega-Cubero S, Pastor MA, Diehl-Schmid J, Alexopoulos P, Benussi L, ... ... Sorbi S, et al. Rare Variants in PLD3 do not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort. Human Mutation. PMID 26411346 DOI: 10.1002/Humu.22908 |
0.435 |
|
| 2015 |
Schmidt R, Hofer E, Bouwman FH, Buerger K, Cordonnier C, Fladby T, Galimberti D, Georges J, Heneka MT, Hort J, Laczó J, Molinuevo JL, O'Brien JT, Religa D, Scheltens P, ... ... Sorbi S, et al. EFNS-ENS/EAN Guideline on concomitant use of cholinesterase inhibitors and memantine in moderate to severe Alzheimer's disease. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 22: 889-98. PMID 25808982 DOI: 10.1111/Ene.12707 |
0.412 |
|
| 2015 |
Cuyvers E, van der Zee J, Bettens K, Engelborghs S, Vandenbulcke M, Robberecht C, Dillen L, Merlin C, Geerts N, Graff C, Thonberg H, Chiang HH, Pastor P, Ortega-Cubero S, Pastor MA, ... ... Sorbi S, et al. Genetic variability in SQSTM1 and risk of early-onset Alzheimer dementia: a European early-onset dementia consortium study. Neurobiology of Aging. 36: 2005.e15-22. PMID 25796131 DOI: 10.1016/J.Neurobiolaging.2015.02.014 |
0.451 |
|
| 2015 |
Rohrer JD, Nicholas JM, Cash DM, van Swieten J, Dopper E, Jiskoot L, van Minkelen R, Rombouts SA, Cardoso MJ, Clegg S, Espak M, Mead S, Thomas DL, De Vita E, Masellis M, ... ... Sorbi S, et al. Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis. The Lancet. Neurology. 14: 253-62. PMID 25662776 DOI: 10.1016/S1474-4422(14)70324-2 |
0.399 |
|
| 2015 |
Borroni B, Turrone R, Galimberti D, Nacmias B, Alberici A, Benussi A, Caffarra P, Caltagirone C, Cappa SF, Frisoni GB, Ghidoni R, Marra C, Padovani A, Rainero I, Scarpini E, ... ... Sorbi S, et al. Italian Frontotemporal Dementia Network (FTD Group-SINDEM): sharing clinical and diagnostic procedures in Frontotemporal Dementia in Italy. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 36: 751-7. PMID 25528460 DOI: 10.1007/S10072-014-2033-9 |
0.338 |
|
| 2015 |
Borroni B, Benussi A, Archetti S, Galimberti D, Parnetti L, Nacmias B, Sorbi S, Scarpini E, Padovani A. Csf p-tau181/tau ratio as biomarker for TDP pathology in frontotemporal dementia. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 16: 86-91. PMID 25352065 DOI: 10.3109/21678421.2014.971812 |
0.338 |
|
| 2015 |
Ghani M, Lang AE, Zinman L, Nacmias B, Sorbi S, Bessi V, Tedde A, Tartaglia MC, Surace EI, Sato C, Moreno D, Xi Z, Hung R, Nalls MA, Singleton A, et al. Mutation analysis of patients with neurodegenerative disorders using NeuroX array. Neurobiology of Aging. 36: 545.e9-14. PMID 25174650 DOI: 10.1016/J.Neurobiolaging.2014.07.038 |
0.403 |
|
| 2015 |
Piaceri I, Raspanti B, Tedde A, Bagnoli S, Sorbi S, Nacmias B. Epigenetic modifications in Alzheimer's disease: cause or effect? Journal of Alzheimer's Disease : Jad. 43: 1169-73. PMID 25159670 DOI: 10.3233/Jad-141452 |
0.419 |
|
| 2015 |
Cash DM, Dick KM, Fellows A, Espak M, Swieten JCv, Galimberti D, Borroni B, Masellis M, Tagliavini F, Graff C, Rowe J, Frisoni GB, Laforce R, Finger E, Sorbi S, et al. MONDAY, JULY 20, 2015 ORAL SESSIONS O2-01 NEUROIMAGING: IMAGING — AUTOSOMAL DOMINANT ALZHEIMER'S DISEASE AND FTLDGrey matter differences in genetic frontotemporal dementia: Results from the genfi study Alzheimers & Dementia. 11. DOI: 10.1016/J.Jalz.2015.07.130 |
0.379 |
|
| 2015 |
Cash DM, Dick KM, Fellows A, Espak M, Swieten JCv, Galimberti D, Borroni B, Masellis M, Tagliavini F, Graff C, Rowe J, Frisoni GB, Laforce R, Finger E, Sorbi S, et al. Grey matter differences in genetic frontotemporal dementia: Results from the genfi study Alzheimers & Dementia. 11: 171. DOI: 10.1016/J.Jalz.2015.06.075 |
0.344 |
|
| 2014 |
Nacmias B, Piaceri I, Bagnoli S, Tedde A, Piacentini S, Sorbi S. Genetics of Alzheimer's Disease and Frontotemporal Dementia. Current Molecular Medicine. PMID 25323872 DOI: 10.2174/1566524014666141010152143 |
0.438 |
|
| 2014 |
Coppedè F, Tannorella P, Tognoni G, Bagnoli S, Bongioanni P, Nacmias B, Siciliano G, Sorbi S, Bonuccelli U, Migliore L. A pilot study evaluating the contribution of SLC19A1 (RFC-1) 80G>a polymorphism to Alzheimer's disease in Italian Caucasians. Biomed Research International. 2014: 608104. PMID 24995314 DOI: 10.1155/2014/608104 |
0.415 |
|
| 2014 |
Ferrari R, Hernandez DG, Nalls MA, Rohrer JD, Ramasamy A, Kwok JB, Dobson-Stone C, Brooks WS, Schofield PR, Halliday GM, Hodges JR, Piguet O, Bartley L, Thompson E, Haan E, ... ... Sorbi S, et al. Frontotemporal dementia and its subtypes: a genome-wide association study. The Lancet. Neurology. 13: 686-99. PMID 24943344 DOI: 10.1016/S1474-4422(14)70065-1 |
0.366 |
|
| 2014 |
Escott-Price V, Bellenguez C, Wang LS, Choi SH, Harold D, Jones L, Holmans P, Gerrish A, Vedernikov A, Richards A, DeStefano AL, Lambert JC, Ibrahim-Verbaas CA, Naj AC, Sims R, ... ... Sorbi S, et al. Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease. Plos One. 9: e94661. PMID 24922517 DOI: 10.1371/Journal.Pone.0094661 |
0.395 |
|
| 2014 |
Bonavita V, Padovani A, Bruni A, Pantoni L, Caltagirone C, Parnetti L, Clerici F, Perani D, Di Luca M, Sorbi S, Forloni G, Tagliavini F, Frisoni G, Tempini MG, Mariani C, et al. Abstracts of the IX Congresso Sindem: Italian Association for the study of Dementia linked to the Italian Neurological Society (SIN), March 13-15, 2014, Florence, Italy. Journal of Alzheimer's Disease : Jad. 41: S1-S68. PMID 24916691 DOI: 10.3233/Jad-149999 |
0.339 |
|
| 2014 |
van der Zee J, Van Langenhove T, Kovacs GG, Dillen L, Deschamps W, Engelborghs S, Mat?j R, Vandenbulcke M, Sieben A, Dermaut B, Smets K, Van Damme P, Merlin C, Laureys A, Van Den Broeck M, ... ... Sorbi S, et al. Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration. Acta Neuropathologica. 128: 397-410. PMID 24899140 DOI: 10.1007/S00401-014-1298-7 |
0.365 |
|
| 2014 |
Bagnoli S, Piaceri I, Sorbi S, Nacmias B. Advances in imaging-genetic relationships for Alzheimer's disease: clinical implications. Neurodegenerative Disease Management. 4: 73-81. PMID 24640981 DOI: 10.2217/Nmt.13.68 |
0.422 |
|
| 2014 |
Spalletta G, Caltagirone C, Padovani A, Sorbi S, Attar M, Colombo D, Cravello L. Cognitive and affective changes in mild to moderate Alzheimer's disease patients undergoing switch of cholinesterase inhibitors: a 6-month observational study. Plos One. 9: e89216. PMID 24586603 DOI: 10.1371/Journal.Pone.0089216 |
0.355 |
|
| 2014 |
Piaceri I, Pradella S, Cupidi C, Nannucci S, Polito C, Bagnoli S, Tedde A, Smirne N, Anfossi M, Gallo M, Bernardi L, Colao R, Maletta R, Bruni AC, Sorbi S, et al. Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degeneration. Journal of Alzheimer's Disease : Jad. 40: 679-85. PMID 24503614 DOI: 10.3233/Jad-132126 |
0.407 |
|
| 2014 |
Fogh I, Ratti A, Gellera C, Lin K, Tiloca C, Moskvina V, Corrado L, Sorarù G, Cereda C, Corti S, Gentilini D, Calini D, Castellotti B, Mazzini L, Querin G, ... ... Sorbi S, et al. A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. Human Molecular Genetics. 23: 2220-31. PMID 24256812 DOI: 10.1093/Hmg/Ddt587 |
0.341 |
|
| 2014 |
Borroni B, Ferrari F, Galimberti D, Nacmias B, Barone C, Bagnoli S, Fenoglio C, Piaceri I, Archetti S, Bonvicini C, Gennarelli M, Turla M, Scarpini E, Sorbi S, Padovani A. Heterozygous TREM2 mutations in frontotemporal dementia. Neurobiology of Aging. 35: 934.e7-10. PMID 24139279 DOI: 10.1016/J.Neurobiolaging.2013.09.017 |
0.404 |
|
| 2014 |
Ferrari C, Nacmias B, Bagnoli S, Piaceri I, Lombardi G, Pradella S, Tedde A, Sorbi S. Imaging and cognitive reserve studies predict dementia in presymptomatic Alzheimer's disease subjects. Neuro-Degenerative Diseases. 13: 157-9. PMID 23942061 DOI: 10.1159/000353690 |
0.428 |
|
| 2014 |
Salvadori E, Poggesi A, Pracucci G, Inzitari D, Pantoni L, Abbate R, Boddi M, Cesari F, Ciolli L, Coppo M, Del Bene A, Diciotti S, Ginestroni A, Giusti B, Gori AM, ... ... Sorbi S, et al. Development and psychometric properties of a neuropsychological battery for mild cognitive impairment with small vessel disease: The VMCI-tuscany study Journal of Alzheimer's Disease. 43: 1313-1323. DOI: 10.3233/Jad-141449 |
0.303 |
|
| 2013 |
Lambert JC, Ibrahim-Verbaas CA, Harold D, Naj AC, Sims R, Bellenguez C, DeStafano AL, Bis JC, Beecham GW, Grenier-Boley B, Russo G, Thorton-Wells TA, Jones N, Smith AV, Chouraki V, ... ... Sorbi S, et al. Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Nature Genetics. 45: 1452-8. PMID 24162737 DOI: 10.1038/Ng.2802 |
0.399 |
|
| 2013 |
Bagnoli S, Piaceri I, Tedde A, Bessi V, Bracco L, Sorbi S, Nacmias B. TOMM40 polymorphisms in Italian Alzheimer's disease and frontotemporal dementia patients. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 34: 995-8. PMID 23546992 DOI: 10.1007/S10072-013-1425-6 |
0.378 |
|
| 2013 |
Galimberti D, Fenoglio C, Serpente M, Villa C, Bonsi R, Arighi A, Fumagalli GG, Del Bo R, Bruni AC, Anfossi M, Clodomiro A, Cupidi C, Nacmias B, Sorbi S, Piaceri I, et al. Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation. Biological Psychiatry. 74: 384-91. PMID 23473366 DOI: 10.1016/J.Biopsych.2013.01.031 |
0.408 |
|
| 2013 |
Piaceri I, Nacmias B, Sorbi S. Genetics of familial and sporadic Alzheimer's disease. Frontiers in Bioscience (Elite Edition). 5: 167-77. PMID 23276979 DOI: 10.2741/E605 |
0.437 |
|
| 2013 |
van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Theuns J, Engelborghs S, Philtjens S, Vandenbulcke M, Sleegers K, Sieben A, Bäumer V, Maes G, Corsmit E, Borroni B, Padovani A, ... ... Sorbi S, ... ... Sorbi S, et al. A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats. Human Mutation. 34: 363-73. PMID 23111906 DOI: 10.1002/Humu.22244 |
0.359 |
|
| 2013 |
Piaceri I, Bagnoli S, Tedde A, Sorbi S, Nacmias B. Ataxia-telangiectasia mutated (ATM) genetic variant in Italian centenarians. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 34: 573-5. PMID 22960875 DOI: 10.1007/S10072-012-1188-5 |
0.346 |
|
| 2013 |
Evangelisti E, Wright D, Zampagni M, Cascella R, Fiorillo C, Bagnoli S, Relini A, Nichino D, Scartabelli T, Nacmias B, Sorbi S, Cecchi C. Lipid rafts mediate amyloid-induced calcium dyshomeostasis and oxidative stress in Alzheimer's disease. Current Alzheimer Research. 10: 143-53. PMID 22950913 DOI: 10.2174/1567205011310020004 |
0.337 |
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| 2013 |
Polito L, Kehoe PG, Davin A, Benussi L, Ghidoni R, Binetti G, Quadri P, Lucca U, Tettamanti M, Clerici F, Bagnoli S, Galimberti D, Nacmias B, Sorbi S, Guaita A, et al. The SIRT2 polymorphism rs10410544 and risk of Alzheimer's disease in two Caucasian case-control cohorts. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 9: 392-9. PMID 22651940 DOI: 10.1016/J.Jalz.2012.02.003 |
0.372 |
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| 2013 |
Ferrari C, Xu WL, Wang HX, Winblad B, Sorbi S, Qiu C, Fratiglioni L. How can elderly apolipoprotein E ε4 carriers remain free from dementia? Neurobiology of Aging. 34: 13-21. PMID 22503000 DOI: 10.1016/J.Neurobiolaging.2012.03.003 |
0.392 |
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| 2013 |
Lambert JC, Grenier-Boley B, Harold D, Zelenika D, Chouraki V, Kamatani Y, Sleegers K, Ikram MA, Hiltunen M, Reitz C, Mateo I, Feulner T, Bullido M, Galimberti D, Concari L, ... ... Sorbi S, et al. Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease. Molecular Psychiatry. 18: 461-70. PMID 22430674 DOI: 10.1038/Mp.2012.14 |
0.405 |
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| 2013 |
Lambert JC, Grenier-Boley B, Harold D, Zelenika D, Chouraki V, Kamatani Y, Sleegers K, Ikram MA, Hiltunen M, Reitz C, Mateo I, Feulner T, Bullido M, Galimberti D, Concari L, ... ... Sorbi S, et al. Erratum: Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease (Molecular Psychiatry (2013) 18 (521) DOI: 10.1038/mp.2012.75)) Molecular Psychiatry. 18. DOI: 10.1038/Mp.2012.75 |
0.36 |
|
| 2013 |
Nacmias B, Berti V, Piaceri I, Sorbi S. FDG PET and the genetics of dementia Clinical and Translational Imaging. 1: 235-246. DOI: 10.1007/S40336-013-0028-9 |
0.406 |
|
| 2012 |
Filippi M, Agosta F, Barkhof F, Dubois B, Fox NC, Frisoni GB, Jack CR, Johannsen P, Miller BL, Nestor PJ, Scheltens P, Sorbi S, Teipel S, Thompson PM, Wahlund LO, et al. EFNS task force: the use of neuroimaging in the diagnosis of dementia. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 19: e131-40, 1487-501. PMID 22900895 DOI: 10.1111/J.1468-1331.2012.03859.X |
0.39 |
|
| 2012 |
Sorbi S, Hort J, Erkinjuntti T, Fladby T, Gainotti G, Gurvit H, Nacmias B, Pasquier F, Popescu BO, Rektorova I, Religa D, Rusina R, Rossor M, Schmidt R, Stefanova E, et al. EFNS-ENS Guidelines on the diagnosis and management of disorders associated with dementia. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 19: 1159-79. PMID 22891773 DOI: 10.1111/J.1468-1331.2012.03784.X |
0.386 |
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| 2012 |
Tedde A, Piaceri I, Bagnoli S, Lucenteforte E, Piacentini S, Sorbi S, Nacmias B. DAPK1 is associated with FTD and not with Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 32: 13-7. PMID 22785394 DOI: 10.3233/Jad-2012-120556 |
0.392 |
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| 2012 |
Bagnoli S, Failli Y, Piaceri I, Rinnoci V, Bessi V, Tedde A, Nacmias B, Sorbi S. Suitability of neuropsychological tests in patients with vascular dementia (VaD). Journal of the Neurological Sciences. 322: 41-5. PMID 22694976 DOI: 10.1016/J.Jns.2012.05.045 |
0.345 |
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| 2012 |
Piaceri I, Rinnoci V, Bagnoli S, Failli Y, Sorbi S. Mitochondria and Alzheimer's disease. Journal of the Neurological Sciences. 322: 31-4. PMID 22694975 DOI: 10.1016/J.Jns.2012.05.033 |
0.393 |
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| 2012 |
Filippi M, Agosta F, Frisoni GB, De Stefano N, Bizzi A, Bozzali M, Falini A, Rocca MA, Sorbi S, Caltagirone C, Tedeschi G. Magnetic resonance imaging in Alzheimer's disease: from diagnosis to monitoring treatment effect. Current Alzheimer Research. 9: 1198-209. PMID 22515495 DOI: 10.2174/156720512804142949 |
0.391 |
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| 2012 |
Castellini G, Ricca V, Lelli L, Bagnoli S, Lucenteforte E, Faravelli C, Sorbi S, Nacmias B. Association between serotonin transporter gene polymorphism and eating disorders outcome: a 6-year follow-up study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 491-500. PMID 22488946 DOI: 10.1002/Ajmg.B.32052 |
0.322 |
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| 2012 |
Zampagni M, Wright D, Cascella R, D'Adamio G, Casamenti F, Evangelisti E, Cardona F, Goti A, Nacmias B, Sorbi S, Liguri G, Cecchi C. Novel S-acyl glutathione derivatives prevent amyloid oxidative stress and cholinergic dysfunction in Alzheimer disease models. Free Radical Biology & Medicine. 52: 1362-71. PMID 22326489 DOI: 10.1016/J.Freeradbiomed.2012.01.012 |
0.351 |
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| 2012 |
Coppedè F, Zitarosa MT, Migheli F, Lo Gerfo A, Bagnoli S, Dardano A, Nacmias B, Mancuso M, Monzani F, Siciliano G, Sorbi S, Migliore L. DNMT3B promoter polymorphisms and risk of late onset Alzheimer's disease. Current Alzheimer Research. 9: 550-4. PMID 22272627 DOI: 10.2174/156720512800618062 |
0.377 |
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| 2012 |
Garibotto V, Borroni B, Sorbi S, Cappa SF, Padovani A, Perani D. Education and occupation provide reserve in both ApoE ε4 carrier and noncarrier patients with probable Alzheimer's disease. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 33: 1037-42. PMID 22173784 DOI: 10.1007/S10072-011-0889-5 |
0.381 |
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| 2012 |
Musicco M, Padovani A, Sorbi S, Scarpini E, Caffarra P, Cappa S, Clerici F, Tabaton M, Caltagirone C, Bonavita V, Bruni AC, Bruno G, Federico A, Ferrarese C, Marra C, et al. Position paper of the Italian Society for the study of Dementias (SINDEM) on the proposal of a new lexicon on Alzheimer disease. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 33: 201-8. PMID 22057264 DOI: 10.1007/S10072-011-0825-8 |
0.393 |
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| 2012 |
Coppedè F, Tannorella P, Pezzini I, Migheli F, Ricci G, Caldarazzo lenco E, Piaceri I, Polini A, Nacmias B, Monzani F, Sorbi S, Siciliano G, Migliore L. Folate, homocysteine, vitamin B12, and polymorphisms of genes participating in one-carbon metabolism in late-onset Alzheimer's disease patients and healthy controls. Antioxidants & Redox Signaling. 17: 195-204. PMID 22034983 DOI: 10.1089/Ars.2011.4368 |
0.343 |
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| 2012 |
Bagnoli S, Piaceri I, Tedde A, Piacentini S, Nannucci S, Bracco L, Sorbi S, Nacmias B. Progranulin genetic screening in frontotemporal lobar degeneration patients from central Italy. Cellular and Molecular Neurobiology. 32: 13-6. PMID 21800185 DOI: 10.1007/S10571-011-9741-Y |
0.357 |
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| 2012 |
Piaceri I, Del Mastio M, Tedde A, Bagnoli S, Latorraca S, Massaro F, Paganini M, Corrado A, Sorbi S, Nacmias B. Clinical heterogeneity in Italian patients with amyotrophic lateral sclerosis. Clinical Genetics. 82: 83-7. PMID 21651514 DOI: 10.1111/J.1399-0004.2011.01726.X |
0.337 |
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| 2012 |
Portaccio E, Razzolini L, Goretti B, Battaglini M, Stromillo ML, Siracusa G, Giorgio A, Hakiki B, Giannini M, Pasto L, Sorbi S, Federico A, Stefano ND, Amato M. Cognitive Reserve Theory May Apply to the Model of Multiple Sclerosis (P03.070) Neurology. 78. DOI: 10.1212/Wnl.78.1_Meetingabstracts.P03.070 |
0.308 |
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| 2012 |
Frisoni GB, Tagliavini F, Sorbi S, Padovani A, Scarpini E, Babiloni C, Pievani M, Bruni AC. 9 Let's treat Alzheimer's disease - genetic aspects Neurobiology of Aging. 33. DOI: 10.1016/J.Neurobiolaging.2012.01.027 |
0.368 |
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| 2012 |
Spalletta G, Caltagirone C, Padovani A, Sorbi S, Attar M, Colombo D. Cognitive and affective changes in mild-to-moderate Alzheimer's disease patients undergoing switch of cholinesterase inhibitors enrolled in the EVOLUTION study: The effect of different inhibitor/formulation Alzheimers & Dementia. 8. DOI: 10.1016/J.Jalz.2013.08.059 |
0.356 |
|
| 2012 |
Xu W, Ferrari C, Wang H, Sorbi S, Winblad B, Qiu C, Fratiglioni L. How can elderly APOE-ε4 carriers remain free from dementia? Alzheimers & Dementia. 8: 629. DOI: 10.1016/J.Jalz.2012.05.1679 |
0.331 |
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| 2011 |
Sierant M, Paduszynska A, Kazmierczak-Baranska J, Nacmias B, Sorbi S, Bagnoli S, Sochacka E, Nawrot B. Specific Silencing of L392V PSEN1 Mutant Allele by RNA Interference. International Journal of Alzheimer's Disease. 2011: 809218. PMID 21559198 DOI: 10.4061/2011/809218 |
0.302 |
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| 2011 |
Tedde A, Piaceri I, Bagnoli S, Lucenteforte E, Ueberham U, Arendt T, Sorbi S, Nacmias B. Association Study of Genetic Variants in CDKN2A/CDKN2B Genes/Loci with Late-Onset Alzheimer's Disease. International Journal of Alzheimer's Disease. 2011: 374631. PMID 21559192 DOI: 10.4061/2011/374631 |
0.457 |
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| 2011 |
Genin E, Hannequin D, Wallon D, Sleegers K, Hiltunen M, Combarros O, Bullido MJ, Engelborghs S, De Deyn P, Berr C, Pasquier F, Dubois B, Tognoni G, Fiévet N, Brouwers N, ... ... Sorbi S, et al. APOE and Alzheimer disease: a major gene with semi-dominant inheritance. Molecular Psychiatry. 16: 903-7. PMID 21556001 DOI: 10.1038/Mp.2011.52 |
0.394 |
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| 2011 |
Hollingworth P, Harold D, Sims R, Gerrish A, Lambert JC, Carrasquillo MM, Abraham R, Hamshere ML, Pahwa JS, Moskvina V, Dowzell K, Jones N, Stretton A, Thomas C, Richards A, ... ... Sorbi S, et al. Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nature Genetics. 43: 429-35. PMID 21460840 DOI: 10.1038/Ng.803 |
0.319 |
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| 2011 |
Piaceri I, Bagnoli S, Lucenteforte E, Mancuso M, Tedde A, Siciliano G, Piacentini S, Bracco L, Sorbi S, Nacmias B. Implication of a genetic variant at PICALM in Alzheimer’s disease patients and centenarians. Journal of Alzheimer's Disease : Jad. 24: 409-13. PMID 21297266 DOI: 10.3233/Jad-2011-101791 |
0.364 |
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| 2011 |
Lescai F, Chiamenti AM, Codemo A, Pirazzini C, D'Agostino G, Ruaro C, Ghidoni R, Benussi L, Galimberti D, Esposito F, Marchegiani F, Cardelli M, Olivieri F, Nacmias B, Sorbi S, et al. An APOE haplotype associated with decreased ε4 expression increases the risk of late onset Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 24: 235-45. PMID 21263195 DOI: 10.3233/Jad-2011-101764 |
0.414 |
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| 2011 |
Reitz C, Cheng R, Rogaeva E, Lee JH, Tokuhiro S, Zou F, Bettens K, Sleegers K, Tan EK, Kimura R, Shibata N, Arai H, Kamboh MI, Prince JA, Maier W, ... ... Sorbi S, et al. Meta-analysis of the association between variants in SORL1 and Alzheimer disease. Archives of Neurology. 68: 99-106. PMID 21220680 DOI: 10.1001/Archneurol.2010.346 |
0.398 |
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| 2011 |
Lambert JC, Zelenika D, Hiltunen M, Chouraki V, Combarros O, Bullido MJ, Tognoni G, Fiévet N, Boland A, Arosio B, Coto E, Del Zompo M, Mateo I, Frank-Garcia A, Helisalmi S, ... ... Sorbi S, et al. Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations. Neurobiology of Aging. 32: 756.e11-5. PMID 21220176 DOI: 10.1016/J.Neurobiolaging.2010.11.022 |
0.384 |
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| 2011 |
Marini S, Bagnoli S, Bessi V, Tedde A, Bracco L, Sorbi S, Nacmias B. Implication of serotonin-transporter (5-HTT) gene polymorphism in subjective memory complaints and mild cognitive impairment (MCI). Archives of Gerontology and Geriatrics. 52: e71-4. PMID 20599283 DOI: 10.1016/J.Archger.2010.06.006 |
0.339 |
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| 2011 |
Pensalfini A, Zampagni M, Liguri G, Becatti M, Evangelisti E, Fiorillo C, Bagnoli S, Cellini E, Nacmias B, Sorbi S, Cecchi C. Membrane cholesterol enrichment prevents Aβ-induced oxidative stress in Alzheimer's fibroblasts. Neurobiology of Aging. 32: 210-22. PMID 19297055 DOI: 10.1016/J.Neurobiolaging.2009.02.010 |
0.302 |
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| 2011 |
Bonavita V, Caltagirone C, Mariani C, Padovani A, Scarpini E, Sorbi S. VI Sindem MEETING: Italian Association for the Study of Dementia linked to the Italian Neurological Society (SIN) Journal of Alzheimer's Disease. 23: S1-S87. DOI: 10.3233/Jad-2010-1433 |
0.334 |
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| 2010 |
Lambert JC, Sleegers K, González-Pérez A, Ingelsson M, Beecham GW, Hiltunen M, Combarros O, Bullido MJ, Brouwers N, Bettens K, Berr C, Pasquier F, Richard F, Dekosky ST, Hannequin D, ... ... Sorbi S, et al. The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study. Journal of Alzheimer's Disease : Jad. 22: 247-55. PMID 20847397 DOI: 10.3233/Jad-2010-100933 |
0.442 |
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| 2010 |
Hort J, O'Brien JT, Gainotti G, Pirttila T, Popescu BO, Rektorova I, Sorbi S, Scheltens P. EFNS guidelines for the diagnosis and management of Alzheimer's disease. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 17: 1236-48. PMID 20831773 DOI: 10.1111/J.1468-1331.2010.03040.X |
0.376 |
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| 2010 |
Santoro A, Balbi V, Balducci E, Pirazzini C, Rosini F, Tavano F, Achilli A, Siviero P, Minicuci N, Bellavista E, Mishto M, Salvioli S, Marchegiani F, Cardelli M, Olivieri F, ... ... Sorbi S, et al. Evidence for sub-haplogroup h5 of mitochondrial DNA as a risk factor for late onset Alzheimer's disease. Plos One. 5: e12037. PMID 20700462 DOI: 10.1371/Journal.Pone.0012037 |
0.386 |
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| 2010 |
Matà S, Muscas GC, Cincotta M, Bartolozzi ML, Ambrosini S, Sorbi S. GAD antibodies associated neurological disorders: incidence and phenotype distribution among neurological inflammatory diseases. Journal of Neuroimmunology. 227: 175-7. PMID 20696484 DOI: 10.1016/J.Jneuroim.2010.07.011 |
0.303 |
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| 2010 |
Bessi V, Bagnoli S, Nacmias B, Tedde A, Sorbi S, Bracco L. Semantic dementia associated with mutation V363I in the tau gene. Journal of the Neurological Sciences. 296: 112-4. PMID 20598713 DOI: 10.1016/J.Jns.2010.06.007 |
0.361 |
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| 2010 |
Lescai F, Pirazzini C, D'Agostino G, Santoro A, Ghidoni R, Benussi L, Galimberti D, Federica E, Marchegiani F, Cardelli M, Olivieri F, Nacmias B, Sorbi S, Bagnoli S, Tagliavini F, et al. Failure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patients. Journal of Alzheimer's Disease : Jad. 21: 385-8. PMID 20555150 DOI: 10.3233/Jad-2010-091516 |
0.383 |
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| 2010 |
Magini A, Urbanelli L, Ciccarone V, Tancini B, Polidoro M, Timperio AM, Zolla L, Tedde A, Sorbi S, Emiliani C. Fibroblasts from PS1 mutated pre-symptomatic subjects and Alzheimer's disease patients share a unique protein levels profile. Journal of Alzheimer's Disease : Jad. 21: 431-44. PMID 20555143 DOI: 10.3233/Jad-2010-091522 |
0.415 |
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| 2010 |
Cellini E, Castellini G, Ricca V, Bagnoli S, Tedde A, Rotella CM, Faravelli C, Sorbi S, Nacmias B. Glucocorticoid receptor gene polymorphisms in Italian patients with eating disorders and obesity. Psychiatric Genetics. 20: 282-8. PMID 20440229 DOI: 10.1097/Ypg.0B013E32833A2142 |
0.312 |
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| 2010 |
Tedde A, Bagnoli S, Piaceri I, Lucenteforte E, Bessi V, Bracco L, Mugelli A, Sorbi S, Nacmias B. Different implication of NEDD9 genetic variant in early and late-onset Alzheimer's disease. Neuroscience Letters. 477: 121-3. PMID 20430066 DOI: 10.1016/J.Neulet.2010.04.046 |
0.441 |
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| 2010 |
Pallanti S, Bernardi S, Raglione LM, Marini P, Ammannati F, Sorbi S, Ramat S. Complex repetitive behavior: punding after bilateral subthalamic nucleus stimulation in Parkinson's disease. Parkinsonism & Related Disorders. 16: 376-80. PMID 20346726 DOI: 10.1016/J.Parkreldis.2010.02.011 |
0.309 |
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| 2010 |
Gratacòs M, EscaramÃs G, Bustamante M, Saus E, Agüera Z, Bayés M, Cellini E, de Cid R, Fernández-Aranda F, Forcano L, González JR, Gorwood P, Hebebrand J, Hinney A, Mercader JM, ... ... Sorbi S, et al. Role of the neurotrophin network in eating disorders' subphenotypes: body mass index and age at onset of the disease. Journal of Psychiatric Research. 44: 834-40. PMID 20219210 DOI: 10.1016/J.Jpsychires.2010.01.009 |
0.367 |
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| 2010 |
Nacmias B, Tedde A, Bagnoli S, Lucenteforte E, Cellini E, Piaceri I, Guarnieri BM, Bessi V, Bracco L, Sorbi S. Lack of implication for CALHM1 P86L common variation in Italian patients with early and late onset Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 20: 37-41. PMID 20164602 DOI: 10.3233/Jad-2010-1345 |
0.456 |
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| 2010 |
Bruni AC, Bernardi L, Colao R, Rubino E, Smirne N, Frangipane F, Terni B, Curcio SA, Mirabelli M, Clodomiro A, Di Lorenzo R, Maletta R, Anfossi M, Gallo M, Geracitano S, ... ... Sorbi S, et al. Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation. Neurology. 74: 798-806. PMID 20164095 DOI: 10.1212/Wnl.0B013E3181D52785 |
0.358 |
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| 2010 |
Santoro A, Siviero P, Minicuci N, Bellavista E, Mishto M, Olivieri F, Marchegiani F, Chiamenti AM, Benussi L, Ghidoni R, Nacmias B, Bagnoli S, Ginestroni A, Scarpino O, Feraco E, ... ... Sorbi S, et al. Effects of donepezil, galantamine and rivastigmine in 938 Italian patients with Alzheimer's disease: a prospective, observational study. Cns Drugs. 24: 163-76. PMID 20088621 DOI: 10.2165/11310960-000000000-00000 |
0.395 |
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| 2010 |
Berti V, Polito C, Ramat S, Vanzi E, De Cristofaro MT, Pellicanò G, Mungai F, Marini P, Formiconi AR, Sorbi S, Pupi A. Brain metabolic correlates of dopaminergic degeneration in de novo idiopathic Parkinson's disease. European Journal of Nuclear Medicine and Molecular Imaging. 37: 537-44. PMID 19727712 DOI: 10.1007/S00259-009-1259-X |
0.308 |
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| 2009 |
Portaccio E, Goretti B, Zipoli V, Nacmias B, Stromillo ML, Bartolozzi ML, Siracusa G, Guidi L, Federico A, Sorbi S, De Stefano N, Amato MP. APOE-epsilon4 is not associated with cognitive impairment in relapsing-remitting multiple sclerosis. Multiple Sclerosis (Houndmills, Basingstoke, England). 15: 1489-94. PMID 19965518 DOI: 10.1177/1352458509348512 |
0.322 |
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| 2009 |
Cellini E, Tedde A, Bagnoli S, Pradella S, Piacentini S, Sorbi S, Nacmias B. Implication of sex and SORL1 variants in italian patients with Alzheimer disease. Archives of Neurology. 66: 1260-6. PMID 19822782 DOI: 10.1001/Archneurol.2009.101 |
0.401 |
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| 2009 |
Portaccio E, Zipoli V, Goretti B, Hakiki B, Nacmias B, Siracusa G, Sorbi S, Amato MP. ApolipoproteinE epsilon 4 allele is not associated with disease course and severity in multiple sclerosis. Acta Neurologica Scandinavica. 120: 439-41. PMID 19804477 DOI: 10.1111/J.1600-0404.2009.01278.X |
0.348 |
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| 2009 |
Lescai F, Blanché H, Nebel A, Beekman M, Sahbatou M, Flachsbart F, Slagboom E, Schreiber S, Sorbi S, Passarino G, Franceschi C. Human longevity and 11p15.5: a study in 1321 centenarians. European Journal of Human Genetics : Ejhg. 17: 1515-9. PMID 19367319 DOI: 10.1038/Ejhg.2009.54 |
0.308 |
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| 2009 |
Nacmias B, Tedde A, Bagnoli S, Cellini E, Guarnieri BM, Piacentini S, Sorbi S. Implication of GAB2 gene polymorphism in Italian patients with Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 16: 513-5. PMID 19276544 DOI: 10.3233/Jad-2009-1005 |
0.428 |
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| 2009 |
Ginestroni A, Battaglini M, Della Nave R, Moretti M, Tessa C, Giannelli M, Caffarra P, Nacmias B, Bessi V, Sorbi S, Bracco L, De Stefano N, Mascalchi M. Early structural changes in individuals at risk of familial Alzheimer's disease: a volumetry and magnetization transfer MR imaging study. Journal of Neurology. 256: 925-32. PMID 19252791 DOI: 10.1007/S00415-009-5044-3 |
0.374 |
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| 2009 |
Giliberto L, Borghi R, Piccini A, Mangerini R, Sorbi S, Cirmena G, Garuti A, Ghetti B, Tagliavini F, Mughal MR, Mattson MP, Zhu X, Wang X, Guglielmotto M, Tamagno E, et al. Mutant presenilin 1 increases the expression and activity of BACE1. The Journal of Biological Chemistry. 284: 9027-38. PMID 19196715 DOI: 10.1074/Jbc.M805685200 |
0.317 |
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| 2009 |
Salmon E, Kerrouche N, Perani D, Lekeu F, Holthoff V, Beuthien-Baumann B, Sorbi S, Lemaire C, Collette F, Herholz K. On the multivariate nature of brain metabolic impairment in Alzheimer's disease. Neurobiology of Aging. 30: 186-97. PMID 17651869 DOI: 10.1016/J.Neurobiolaging.2007.06.010 |
0.364 |
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| 2009 |
Nacmias B, Cellini E, Ricca V, Castellini G, Tedde A, Bagnoli S, Sorbi S. P02-64 Glucocorticoid receptor gene polymorphisms in Italian patients with anorexia and bulimia nervosa European Psychiatry. 24: 1-1. DOI: 10.1016/S0924-9338(09)70987-3 |
0.333 |
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| 2008 |
Garibotto V, Borroni B, Kalbe E, Herholz K, Salmon E, Holtoff V, Sorbi S, Cappa SF, Padovani A, Fazio F, Perani D. Education and occupation as proxies for reserve in aMCI converters and AD: FDG-PET evidence. Neurology. 71: 1342-9. PMID 18936426 DOI: 10.1212/01.Wnl.0000327670.62378.C0 |
0.364 |
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| 2008 |
Tedde A, Putignano AL, Nacmias B, Bagnoli S, Cellini E, Sorbi S. Lack of association between TNF-alpha polymorphisms and Alzheimer's disease in an Italian cohort. Neuroscience Letters. 446: 139-42. PMID 18834925 DOI: 10.1016/J.Neulet.2008.09.044 |
0.371 |
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| 2008 |
Cozza A, Melissari E, Iacopetti P, Mariotti V, Tedde A, Nacmias B, Conte A, Sorbi S, Pellegrini S. SNPs in neurotrophin system genes and Alzheimer's disease in an Italian population. Journal of Alzheimer's Disease : Jad. 15: 61-70. PMID 18780967 DOI: 10.3233/Jad-2008-15105 |
0.403 |
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| 2008 |
Berti V, Pupi A, Ramat S, Vanzi E, De Cristofaro MT, Pellicanò G, Mungai F, Marini P, Sorbi S. Clinical correlation of the binding potential with 123I-FP-CIT in de novo idiopathic Parkinson's disease patients. European Journal of Nuclear Medicine and Molecular Imaging. 35: 2220-6. PMID 18649079 DOI: 10.1007/S00259-008-0872-4 |
0.306 |
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| 2008 |
Tedde A, Laura Putignano A, Bagnoli S, Congregati C, Milla M, Sorbi S, Genuardi M, Papi L. Interleukin-10 promoter polymorphisms influence susceptibility to ulcerative colitis in a gender-specific manner. Scandinavian Journal of Gastroenterology. 43: 712-8. PMID 18569989 DOI: 10.1080/00365520701885507 |
0.309 |
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| 2008 |
Nacmias B, Bessi V, Bagnoli S, Tedde A, Cellini E, Piccini C, Sorbi S, Bracco L. KIBRA gene variants are associated with episodic memory performance in subjective memory complaints. Neuroscience Letters. 436: 145-7. PMID 18378080 DOI: 10.1016/J.Neulet.2008.03.008 |
0.311 |
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| 2008 |
Pensalfini A, Cecchi C, Zampagni M, Becatti M, Favilli F, Paoli P, Catarzi S, Bagnoli S, Nacmias B, Sorbi S, Liguri G. Protective effect of new S-acylglutathione derivatives against amyloid-induced oxidative stress. Free Radical Biology & Medicine. 44: 1624-36. PMID 18294463 DOI: 10.1016/J.Freeradbiomed.2008.01.025 |
0.358 |
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| 2008 |
Mosconi L, Tsui WH, Herholz K, Pupi A, Drzezga A, Lucignani G, Reiman EM, Holthoff V, Kalbe E, Sorbi S, Diehl-Schmid J, Perneczky R, Clerici F, Caselli R, Beuthien-Baumann B, et al. Multicenter standardized 18F-FDG PET diagnosis of mild cognitive impairment, Alzheimer's disease, and other dementias. Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine. 49: 390-8. PMID 18287270 DOI: 10.2967/Jnumed.107.045385 |
0.334 |
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| 2008 |
Poleggi A, Bizzarro A, Acciarri A, Antuono P, Bagnoli S, Cellini E, Forno GD, Giannattasio C, Lauria A, Matera MG, Nacmias B, Puopolo M, Seripa D, Sorbi S, Wekstein DR, et al. Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's disease. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 15: 173-8. PMID 18217885 DOI: 10.1111/J.1468-1331.2007.02021.X |
0.427 |
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| 2008 |
Mercader JM, Saus E, Agüera Z, Bayés M, Boni C, Carreras A, Cellini E, de Cid R, Dierssen M, EscaramÃs G, Fernández-Aranda F, Forcano L, Gallego X, González JR, Gorwood P, ... ... Sorbi S, et al. Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders. Human Molecular Genetics. 17: 1234-44. PMID 18203754 DOI: 10.1016/J.Eurpsy.2008.01.1010 |
0.317 |
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| 2008 |
Salmon E, Perani D, Collette F, Feyers D, Kalbe E, Holthoff V, Sorbi S, Herholz K. A comparison of unawareness in frontotemporal dementia and Alzheimer's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 79: 176-9. PMID 17898032 DOI: 10.1136/Jnnp.2007.122853 |
0.417 |
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| 2008 |
Tedde A, Cellini E, Bagnoli S, Sorbi S, Peri A. Mutational screening analysis of DHCR24/seladin-1 gene in Italian familial Alzheimer's disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 117-9. PMID 17579359 DOI: 10.1002/Ajmg.B.30573 |
0.452 |
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| 2008 |
Urbanelli L, Emiliani C, Massini C, Persichetti E, Orlacchio A, Pelicci G, Sorbi S, Hasilik A, Bernardi G, Orlacchio A. Cathepsin D expression is decreased in Alzheimer's disease fibroblasts. Neurobiology of Aging. 29: 12-22. PMID 17049675 DOI: 10.1016/J.Neurobiolaging.2006.09.005 |
0.396 |
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| 2008 |
Rogaeva E, Lee JH, Meng Y, Wakutani Y, Zou F, Moreno D, Cheng R, Sorbi S, Bruni A, Duara R, Graff-Radford N, Petersen RC, Dickson D, Younkin S, Farrer LA, et al. P3-258: Further evidence of genetic association between SORL1 and Alzheimer's disease Alzheimers & Dementia. 4. DOI: 10.1016/J.Jalz.2008.05.1826 |
0.392 |
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| 2007 |
Bracco L, Piccini C, Baccini M, Bessi V, Biancucci F, Nacmias B, Bagnoli S, Sorbi S. Pattern and progression of cognitive decline in Alzheimer's disease: role of premorbid intelligence and ApoE genotype. Dementia and Geriatric Cognitive Disorders. 24: 483-91. PMID 18025782 DOI: 10.1159/000111081 |
0.35 |
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| 2007 |
Tedde A, Bagnoli S, Cellini E, Nacmias B, Piacentini S, Sorbi S. No association between the LRRK2 G2019S mutation and Alzheimer's disease in Italy. Cellular and Molecular Neurobiology. 27: 877-81. PMID 17846883 DOI: 10.1007/S10571-007-9207-4 |
0.377 |
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| 2007 |
Bellucci C, Lilli C, Baroni T, Parnetti L, Sorbi S, Emiliani C, Lumare E, Calabresi P, Balloni S, Bodo M. Differences in extracellular matrix production and basic fibroblast growth factor response in skin fibroblasts from sporadic and familial Alzheimer's disease. Molecular Medicine (Cambridge, Mass.). 13: 542-50. PMID 17660861 DOI: 10.2119/2007-00034.Bellucci |
0.33 |
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| 2007 |
Bagnoli S, Cellini E, Tedde A, Nacmias B, Piacentini S, Bessi V, Bracco L, Sorbi S. Association of IL10 promoter polymorphism in Italian Alzheimer's disease. Neuroscience Letters. 418: 262-5. PMID 17420099 DOI: 10.1016/J.Neulet.2007.03.030 |
0.393 |
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| 2007 |
Bracco L, Bessi V, Piccini C, Mosconi L, Pupi A, Sorbi S. Metabolic correlates of executive dysfunction. Different patterns in mild and very mild Alzheimer's disease. Journal of Neurology. 254: 1052-65. PMID 17385079 DOI: 10.1007/S00415-006-0488-1 |
0.398 |
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| 2007 |
Brown AM, Gordon D, Lee H, Wavrant-De Vrièze F, Cellini E, Bagnoli S, Nacmias B, Sorbi S, Hardy J, Blass JP. Testing for linkage and association across the dihydrolipoyl dehydrogenase gene region with Alzheimer's disease in three sample populations. Neurochemical Research. 32: 857-69. PMID 17342416 DOI: 10.1007/S11064-006-9235-3 |
0.42 |
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| 2007 |
Rogaeva E, Meng Y, Lee JH, Gu Y, Kawarai T, Zou F, Katayama T, Baldwin CT, Cheng R, Hasegawa H, Chen F, Shibata N, Lunetta KL, Pardossi-Piquard R, Bohm C, ... ... Sorbi S, et al. The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease. Nature Genetics. 39: 168-77. PMID 17220890 DOI: 10.1038/Ng1943 |
0.374 |
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| 2007 |
Nacmias B, Bagnoli S, Tedde A, Cellini E, Bessi V, Guarnieri B, Ortensi L, Piacentini S, Bracco L, Sorbi S. Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity. Archives of Gerontology and Geriatrics. 45: 201-6. PMID 17182125 DOI: 10.1016/J.Archger.2006.10.011 |
0.413 |
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| 2007 |
Shibata N, Kawarai T, Meng Y, Lee JH, Lee HS, Wakutani Y, Shibata E, Pathan N, Bi A, Sato C, Sorbi S, Bruni AC, Duara R, Mayeux R, Farrer LA, et al. Association studies between the plasmin genes and late-onset Alzheimer's disease. Neurobiology of Aging. 28: 1041-3. PMID 16828203 DOI: 10.1016/J.Neurobiolaging.2006.05.028 |
0.437 |
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| 2007 |
Cecchi C, Fiorillo C, Baglioni S, Pensalfini A, Bagnoli S, Nacmias B, Sorbi S, Nosi D, Relini A, Liguri G. Increased susceptibility to amyloid toxicity in familial Alzheimer's fibroblasts. Neurobiology of Aging. 28: 863-76. PMID 16781020 DOI: 10.1016/J.Neurobiolaging.2006.05.014 |
0.346 |
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| 2007 |
Ramat S, Ammannati F, Raglione L-, Marini P, Paganini M, Molteni S, Luzio AESd, Mennonna P, Sorbi S. 3.215 Deep brain stimulation of the subthalamic nucleus for Parkinson's disease: Clinical follow-up of 55 patients Parkinsonism & Related Disorders. 13. DOI: 10.1016/S1353-8020(08)70853-8 |
0.318 |
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| 2007 |
Polito C, Ramat S, Cristofaro MTD, Marini P, Paganini M, Sorbi S, Pupi A. 3.116 Set-shifting deficit and fronto-temporal hypometabolism in early Parkinson's disease Parkinsonism & Related Disorders. 13. DOI: 10.1016/S1353-8020(08)70824-1 |
0.309 |
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| 2006 |
Cellini E, Tedde A, Bagnoli S, Nacmias B, Piacentini S, Bessi V, Bracco L, Sorbi S. Association analysis of the paraoxonase-1 gene with Alzheimer's disease. Neuroscience Letters. 408: 199-202. PMID 16996683 DOI: 10.1016/J.Neulet.2006.08.074 |
0.426 |
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| 2006 |
Cellini E, Forleo P, Ginestroni A, Nacmias B, Tedde A, Bagnoli S, Mascalchi M, Sorbi S, Piacentini S. Fragile X premutation with atypical symptoms at onset. Archives of Neurology. 63: 1135-8. PMID 16908740 DOI: 10.1001/Archneur.63.8.1135 |
0.357 |
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| 2006 |
Peters F, Perani D, Herholz K, Holthoff V, Beuthien-Baumann B, Sorbi S, Pupi A, Degueldre C, Lemaire C, Collette F, Salmon E. Orbitofrontal dysfunction related to both apathy and disinhibition in frontotemporal dementia. Dementia and Geriatric Cognitive Disorders. 21: 373-9. PMID 16534207 DOI: 10.1159/000091898 |
0.307 |
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| 2006 |
Mishto M, Bellavista E, Santoro A, Stolzing A, Ligorio C, Nacmias B, Spazzafumo L, Chiappelli M, Licastro F, Sorbi S, Pession A, Ohm T, Grune T, Franceschi C. Immunoproteasome and LMP2 polymorphism in aged and Alzheimer's disease brains. Neurobiology of Aging. 27: 54-66. PMID 16298241 DOI: 10.1016/J.Neurobiolaging.2004.12.004 |
0.4 |
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| 2006 |
Nacmias B, Bagnoli S, Tedde A, Cellini E, Guarnieri BM, Bartoli A, Serio A, Piacentini S, Sorbi S. Cystatin C and apoe polymorphisms in Italian Alzheimer's disease. Neuroscience Letters. 392: 110-3. PMID 16188386 DOI: 10.1016/J.Neulet.2005.09.006 |
0.44 |
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| 2006 |
Tedde A, Rotondi M, Cellini E, Bagnoli S, Muratore L, Nacmias B, Sorbi S. Lack of association between the CYP46 gene polymorphism and Italian late-onset sporadic Alzheimer's disease. Neurobiology of Aging. 27: 773.e1-773.e3. PMID 16055229 DOI: 10.1016/J.Neurobiolaging.2005.03.029 |
0.42 |
|
| 2006 |
Cellini E, Tedde A, Nacmias B, Bagnoli S, Sorbi S. P1-323: A cholesterol 24S-hydroxylase gene (Cyp46) polymorphism in Italian Alzheimer’s disease patients Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.701 |
0.345 |
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| 2006 |
Bagnoli S, Nacmias B, Cellini E, Tedde A, Bessi V, Sorbi S. P1-291: Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer’s disease and longevity Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.668 |
0.402 |
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| 2006 |
Pizzo P, Zatti G, Burgo A, Giacomello M, Florean C, Sinigaglia G, Barbiero L, Ghidoni R, Bagnoli S, Nacmias B, Sorbi S, Binetti G, Fasolato C. P3-393: Familial Alzheimer's disease presenilin mutants reduce calcium levels of intracellular stores. A critical reevaluation of the “calcium overload” hypothesis Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.1663 |
0.339 |
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| 2006 |
Mosconi L, Pupi A, Leon Md, Li Y, Nacmias B, Santi SD, Tsui W, Myoung P, Bessi V, Fayyaz M, Mascalchi M, Sorbi S. P2-314: Hypometabolism precedes volume loss in presymptomatic individuals with early-onset familial Alzheimer’s disease Alzheimers & Dementia. 2. DOI: 10.1016/J.Jalz.2006.05.1154 |
0.322 |
|
| 2005 |
Cellini E, Bagnoli S, Tedde A, Nacmias B, Piacentini S, Sorbi S. Insulin degrading enzyme and alpha-3 catenin polymorphisms in Italian patients with Alzheimer disease. Alzheimer Disease and Associated Disorders. 19: 246-7. PMID 16327352 DOI: 10.1097/01.Wad.0000189030.50826.86 |
0.322 |
|
| 2005 |
Anchisi D, Borroni B, Franceschi M, Kerrouche N, Kalbe E, Beuthien-Beumann B, Cappa S, Lenz O, Ludecke S, Marcone A, Mielke R, Ortelli P, Padovani A, Pelati O, Pupi A, ... ... Sorbi S, et al. Heterogeneity of brain glucose metabolism in mild cognitive impairment and clinical progression to Alzheimer disease. Archives of Neurology. 62: 1728-33. PMID 16286547 DOI: 10.1001/Archneur.62.11.1728 |
0.383 |
|
| 2005 |
Bracco L, Piccini C, Moretti M, Mascalchi M, Sforza A, Nacmias B, Cellini E, Bagnoli S, Sorbi S. Alzheimer's disease: role of size and location of white matter changes in determining cognitive deficits. Dementia and Geriatric Cognitive Disorders. 20: 358-66. PMID 16192726 DOI: 10.1159/000088562 |
0.397 |
|
| 2005 |
Pupi A, Mosconi L, Nobili FM, Sorbi S. Toward the validation of functional neuroimaging as a potential biomarker for Alzheimer's disease: implications for drug development. Molecular Imaging and Biology : Mib : the Official Publication of the Academy of Molecular Imaging. 7: 59-68. PMID 15912277 DOI: 10.1007/S11307-005-0953-8 |
0.384 |
|
| 2005 |
Cellini E, Nacmias B, Olivieri F, Ortenzi L, Tedde A, Bagnoli S, Petruzzi C, Franceschi C, Sorbi S. Cholesteryl ester transfer protein (CETP) I405V polymorphism and longevity in Italian centenarians. Mechanisms of Ageing and Development. 126: 826-8. PMID 15888337 DOI: 10.1016/J.Mad.2005.01.009 |
0.324 |
|
| 2005 |
Sorbi S. Beta-amyloid immunisation in Alzheimer's disease. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 26: S5. PMID 15883696 DOI: 10.1007/S10072-005-0388-7 |
0.332 |
|
| 2005 |
Orlacchio A, Kawarai T, Gaudiello F, Totaro A, Schillaci O, Stefani A, Floris R, St George-Hyslop PH, Sorbi S, Bernardi G. Clinical and genetic study of a large SPG4 Italian family. Movement Disorders : Official Journal of the Movement Disorder Society. 20: 1055-9. PMID 15858810 DOI: 10.1002/Mds.20494 |
0.34 |
|
| 2005 |
Kalbe E, Salmon E, Perani D, Holthoff V, Sorbi S, Elsner A, Weisenbach S, Brand M, Lenz O, Kessler J, Luedecke S, Ortelli P, Herholz K. Anosognosia in very mild Alzheimer's disease but not in mild cognitive impairment. Dementia and Geriatric Cognitive Disorders. 19: 349-56. PMID 15802909 DOI: 10.1159/000084704 |
0.36 |
|
| 2005 |
Holthoff VA, Beuthien-Baumann B, Kalbe E, Lüdecke S, Lenz O, Zündorf G, Spirling S, Schierz K, Winiecki P, Sorbi S, Herholz K. Regional cerebral metabolism in early Alzheimer's disease with clinically significant apathy or depression. Biological Psychiatry. 57: 412-21. PMID 15705358 DOI: 10.1016/J.Biopsych.2004.11.035 |
0.367 |
|
| 2005 |
Ribasés M, Gratacòs M, Fernández-Aranda F, Bellodi L, Boni C, Anderluh M, Cristina Cavallini M, Cellini E, Di Bella D, Erzegovesi S, Foulon C, Gabrovsek M, Gorwood P, Hebebrand J, Hinney A, ... ... Sorbi S, et al. Association of BDNF with restricting anorexia nervosa and minimum body mass index: a family-based association study of eight European populations. European Journal of Human Genetics : Ejhg. 13: 428-34. PMID 15657604 DOI: 10.1038/Sj.Ejhg.5201351 |
0.308 |
|
| 2005 |
Bagnoli S, Tedde A, Cellini E, Rotondi M, Nacmias B, Sorbi S. The urokinase-plasminogen activator (PLAU) gene is not associated with late onset Alzheimer's disease. Neurogenetics. 6: 53-4. PMID 15616835 DOI: 10.1007/S10048-004-0203-2 |
0.39 |
|
| 2005 |
Mosconi L, Herholz K, Prohovnik I, Nacmias B, De Cristofaro MT, Fayyaz M, Bracco L, Sorbi S, Pupi A. Metabolic interaction between ApoE genotype and onset age in Alzheimer's disease: implications for brain reserve. Journal of Neurology, Neurosurgery, and Psychiatry. 76: 15-23. PMID 15607989 DOI: 10.1136/Jnnp.2003.030882 |
0.41 |
|
| 2004 |
Musicco M, Sorbi S, Bonavita V, Caltagirone C. Validation of the Guidelines for the Diagnosis of Dementia and Alzheimer's Disease of the Italian Neurological Society. Study in 72 Italian neurological centres and 1549 patients. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 25: 289-95. PMID 15624087 DOI: 10.1007/S10072-004-0356-7 |
0.371 |
|
| 2004 |
Mosconi L, Perani D, Sorbi S, Herholz K, Nacmias B, Holthoff V, Salmon E, Baron JC, De Cristofaro MT, Padovani A, Borroni B, Franceschi M, Bracco L, Pupi A. MCI conversion to dementia and the APOE genotype: a prediction study with FDG-PET. Neurology. 63: 2332-40. PMID 15623696 DOI: 10.1212/01.Wnl.0000147469.18313.3B |
0.368 |
|
| 2004 |
Nacmias B, Piccini C, Bagnoli S, Tedde A, Cellini E, Bracco L, Sorbi S. Brain-derived neurotrophic factor, apolipoprotein E genetic variants and cognitive performance in Alzheimer's disease. Neuroscience Letters. 367: 379-83. PMID 15337270 DOI: 10.1016/J.Neulet.2004.06.039 |
0.407 |
|
| 2004 |
Ricca V, Nacmias B, Boldrini M, Cellini E, di Bernardo M, Ravaldi C, Tedde A, Bagnoli S, Placidi GF, Rotella CM, Sorbi S. Psychopathological traits and 5-HT2A receptor promoter polymorphism (-1438 G/A) in patients suffering from Anorexia Nervosa and Bulimia Nervosa. Neuroscience Letters. 365: 92-6. PMID 15245785 DOI: 10.1016/J.Neulet.2004.04.057 |
0.309 |
|
| 2004 |
Cellini E, Forleo P, Nacmias B, Tedde A, Bagnoli S, Piacentini S, Sorbi S. Spinocerebellar ataxia type 17 repeat in patients with Huntington's disease-like and ataxia. Annals of Neurology. 56: 163; author reply 16. PMID 15236416 DOI: 10.1002/Ana.20146 |
0.341 |
|
| 2004 |
Bonafé M, Salvioli S, Barbi C, Trapassi C, Tocco F, Storci G, Invidia L, Vannini I, Rossi M, Marzi E, Mishto M, Capri M, Olivieri F, Antonicelli R, Memo M, ... ... Sorbi S, et al. The different apoptotic potential of the p53 codon 72 alleles increases with age and modulates in vivo ischaemia-induced cell death. Cell Death and Differentiation. 11: 962-73. PMID 15131588 DOI: 10.1038/Sj.Cdd.4401415 |
0.302 |
|
| 2004 |
Ribasés M, Gratacòs M, Fernández-Aranda F, Bellodi L, Boni C, Anderluh M, Cavallini MC, Cellini E, Di Bella D, Erzegovesi S, Foulon C, Gabrovsek M, Gorwood P, Hebebrand J, Hinney A, ... ... Sorbi S, et al. Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations. Human Molecular Genetics. 13: 1205-12. PMID 15115760 DOI: 10.1093/Hmg/Ddh137 |
0.31 |
|
| 2004 |
De Stefano N, Bartolozzi ML, Nacmias B, Zipoli V, Mortilla M, Guidi L, Siracusa G, Sorbi S, Federico A, Amato MP. Influence of apolipoprotein E epsilon4 genotype on brain tissue integrity in relapsing-remitting multiple sclerosis. Archives of Neurology. 61: 536-40. PMID 15096402 DOI: 10.1001/Archneur.61.4.536 |
0.38 |
|
| 2004 |
Marcon G, Giaccone G, Cupidi C, Balestrieri M, Beltrami CA, Finato N, Bergonzi P, Sorbi S, Bugiani O, Tagliavini F. Neuropathological and clinical phenotype of an Italian Alzheimer family with M239V mutation of presenilin 2 gene. Journal of Neuropathology and Experimental Neurology. 63: 199-209. PMID 15055444 DOI: 10.1093/Jnen/63.3.199 |
0.442 |
|
| 2004 |
Mosconi L, Sorbi S, Nacmias B, De Cristofaro MT, Fayyaz M, Bracco L, Herholz K, Pupi A. Age and ApoE genotype interaction in Alzheimer's disease: an FDG-PET study. Psychiatry Research. 130: 141-51. PMID 15033184 DOI: 10.1016/J.Pscychresns.2003.12.005 |
0.376 |
|
| 2004 |
Piccini A, Fassio A, Pasqualetto E, Vitali A, Borghi R, Palmieri D, Nacmias B, Sorbi S, Sitia R, Tabaton M. Fibroblasts from FAD-linked presenilin 1 mutations display a normal unfolded protein response but overproduce Abeta42 in response to tunicamycin. Neurobiology of Disease. 15: 380-6. PMID 15006708 DOI: 10.1016/J.Nbd.2003.11.013 |
0.318 |
|
| 2004 |
Bagnoli S, Nacmias B, Tedde A, Guarnieri BM, Cellini E, Petruzzi C, Bartoli A, Ortenzi L, Sorbi S. Brain-derived neurotrophic factor genetic variants are not susceptibility factors to Alzheimer's disease in Italy. Annals of Neurology. 55: 447-8. PMID 14991827 DOI: 10.1002/Ana.10842 |
0.359 |
|
| 2004 |
Mosconi L, Nacmias B, Sorbi S, De Cristofaro MT, Fayazz M, Tedde A, Bracco L, Herholz K, Pupi A. Brain metabolic decreases related to the dose of the ApoE e4 allele in Alzheimer's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 75: 370-6. PMID 14966149 DOI: 10.1136/Jnnp.2003.014993 |
0.413 |
|
| 2004 |
Gabrovsek M, Brecelj-Anderluh M, Bellodi L, Cellini E, Di Bella D, Estivill X, Fernandez-Aranda F, Freeman B, Geller F, Gratacos M, Haigh R, Hebebrand J, Hinney A, Holliday J, Hu X, ... ... Sorbi S, et al. Combined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 124: 68-72. PMID 14681918 DOI: 10.1002/Ajmg.B.20085 |
0.33 |
|
| 2004 |
Orlacchio A, Urbanelli L, Mencarelli S, Orlacchio A, Pelicci G, Sorbi S, Hasilik A, Bernardi G, Emiliani C. P4-186 Regulation of lysosomal enzymes expression in fibroblasts from Alzheimer's disease patients Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)81744-5 |
0.353 |
|
| 2004 |
Mosconi L, Pupi A, Sorbi S, Holthoff V, Perani D, Salmon E, Baron JC, Nacmias B, Piccini C, Bracco L, Herholz K. P2-152 Basal frontal/temporal hypometabolism and depressive symptoms in highly educated Alzheimer's disease patients Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)80899-6 |
0.327 |
|
| 2004 |
Rogaeva E, Meng Y, Toulina A, Shibata N, Kawarai T, Sato C, Salehi-Rad S, Morgan A, Rivoiro C, Liang Y, Sorbi S, Bruni AC, Oene MV, Lee J, Mayeux R, et al. S2-01-03 Genetic studies in late-onset Alzheimer disease: loci on chromosomes 12 and 10 Neurobiology of Aging. 25. DOI: 10.1016/S0197-4580(04)80081-2 |
0.37 |
|
| 2003 |
Tedde A, Nacmias B, Ciantelli M, Forleo P, Cellini E, Bagnoli S, Piccini C, Caffarra P, Ghidoni E, Paganini M, Bracco L, Sorbi S. Identification of new presenilin gene mutations in early-onset familial Alzheimer disease. Archives of Neurology. 60: 1541-4. PMID 14623725 DOI: 10.1001/Archneur.60.11.1541 |
0.358 |
|
| 2003 |
Mosconi L, Sorbi S, Nacmias B, De Cristofaro MT, Fayyaz M, Cellini E, Bagnoli S, Bracco L, Herholz K, Pupi A. Brain metabolic differences between sporadic and familial Alzheimer's disease. Neurology. 61: 1138-40. PMID 14581683 DOI: 10.1212/01.Wnl.0000086816.30011.75 |
0.43 |
|
| 2003 |
Emiliani C, Urbanelli L, Racanicchi L, Orlacchio A, Pelicci G, Sorbi S, Bernardi G, Orlacchio A. Up-regulation of glycohydrolases in Alzheimer's Disease fibroblasts correlates with Ras activation. The Journal of Biological Chemistry. 278: 38453-60. PMID 12878600 DOI: 10.1074/Jbc.M303030200 |
0.36 |
|
| 2003 |
Di Natale M, Perri M, Kawarai T, Maletta R, Tomaino C, Sato C, Nacmias B, Shibata N, Sorbi S, St George-Hyslop PH, Bruni AC, Rogaeva E. Absence of association between Alzheimer disease and the regulatory region polymorphism of the PS2 gene in an Italian population. Neuroscience Letters. 343: 210-2. PMID 12770698 DOI: 10.1016/S0304-3940(03)00335-5 |
0.429 |
|
| 2002 |
Cellini E, Piacentini S, Nacmias B, Forleo P, Tedde A, Bagnoli S, Ciantelli M, Sorbi S. A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia. Archives of Neurology. 59: 1952-3. PMID 12470185 DOI: 10.1001/Archneur.59.12.1952 |
0.343 |
|
| 2002 |
Cecchi C, Fiorillo C, Sorbi S, Latorraca S, Nacmias B, Bagnoli S, Nassi P, Liguri G. Oxidative stress and reduced antioxidant defenses in peripheral cells from familial Alzheimer's patients. Free Radical Biology & Medicine. 33: 1372-9. PMID 12419469 DOI: 10.1016/S0891-5849(02)01049-3 |
0.381 |
|
| 2002 |
Bagnoli S, Nacmias B, Tedde A, Guarnieri BM, Cellini E, Ciantelli M, Petruzzi C, Bartoli A, Ortenzi L, Serio A, Sorbi S. Cathepsin D polymorphism in Italian sporadic and familial Alzheimer's disease. Neuroscience Letters. 328: 273-6. PMID 12147324 DOI: 10.1016/S0304-3940(02)00547-5 |
0.452 |
|
| 2002 |
Orlacchio A, Kawarai T, Paciotti E, Stefani A, Orlacchio A, Sorbi S, St George-Hyslop PH, Bernardi G. Association study of the 5-hydroxytryptamine(6) receptor gene in Alzheimer's disease. Neuroscience Letters. 325: 13-6. PMID 12023056 DOI: 10.1016/S0304-3940(02)00221-5 |
0.362 |
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| 2002 |
Scali C, Prosperi C, Bracco L, Piccini C, Baronti R, Ginestroni A, Sorbi S, Pepeu G, Casamenti F. Neutrophils CD11b and fibroblasts PGE(2) are elevated in Alzheimer's disease. Neurobiology of Aging. 23: 523-30. PMID 12009501 DOI: 10.1016/S0197-4580(01)00346-3 |
0.406 |
|
| 2002 |
Ricca V, Nacmias B, Cellini E, Di Bernardo M, Rotella CM, Sorbi S. 5-HT2A receptor gene polymorphism and eating disorders. Neuroscience Letters. 323: 105-8. PMID 11950504 DOI: 10.1016/S0304-3940(02)00088-5 |
0.306 |
|
| 2002 |
Gorwood P, Adès J, Bellodi L, Cellini E, Collier DA, Di Bella D, Di Bernardo M, Estivill X, Fernandez-Aranda F, Gratacos M, Hebebrand J, Hinney A, Hu X, Karwautz A, Kipman A, ... ... Sorbi S, et al. The 5-HT(2A) -1438G/A polymorphism in anorexia nervosa: a combined analysis of 316 trios from six European centres. Molecular Psychiatry. 7: 90-4. PMID 11803452 DOI: 10.1038/Sj/Mp/4000938 |
0.315 |
|
| 2001 |
Cellini E, Forleo P, Nacmias B, Tedde A, Latorraca S, Piacentini S, Parnetti L, Gallai V, Sorbi S. Clinical and genetic analysis of hereditary and sporadic ataxia in central Italy. Brain Research Bulletin. 56: 363-6. PMID 11719273 DOI: 10.1016/S0361-9230(01)00650-5 |
0.374 |
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| 2001 |
Nicolaou M, Song YQ, Sato CA, Orlacchio A, Kawarai T, Medeiros H, Liang Y, Sorbi S, Richard E, Rogaev EI, Moliaka Y, Bruni AC, Jorge R, Percy M, Duara R, et al. Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease. Neurogenetics. 3: 203-6. PMID 11714100 DOI: 10.1007/S100480100123 |
0.402 |
|
| 2001 |
Brunelli T, Bagnoli S, Giusti B, Nacmias B, Pepe G, Sorbi S, Abbate R. The C677T methylenetetrahydrofolate reductase mutation is not associated with Alzheimer's disease. Neuroscience Letters. 315: 103-5. PMID 11711225 DOI: 10.1016/S0304-3940(01)02316-3 |
0.425 |
|
| 2001 |
Cellini E, Nacmias B, Forleo P, Piacentini S, Guarnieri BM, Serio A, Calabrò A, Renzi D, Sorbi S. Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Italy. Archives of Neurology. 58: 1856-9. PMID 11708995 DOI: 10.1001/Archneur.58.11.1856 |
0.384 |
|
| 2001 |
Amato MP, Ponziani G, Siracusa G, Sorbi S. Cognitive dysfunction in early-onset multiple sclerosis: a reappraisal after 10 years. Archives of Neurology. 58: 1602-6. PMID 11594918 DOI: 10.1001/Archneur.58.10.1602 |
0.315 |
|
| 2001 |
Sorbi S, Forleo P, Tedde A, Cellini E, Ciantelli M, Bagnoli S, Nacmias B. Genetic risk factors in familial Alzheimer's disease. Mechanisms of Ageing and Development. 122: 1951-60. PMID 11589913 DOI: 10.1016/S0047-6374(01)00308-6 |
0.406 |
|
| 2001 |
Forleo P, Cellini E, Parnetti L, Murasecco D, Gallai V, Nacmias B, Sorbi S. Clinical and genetic analysis of an Italian family with Machado-Joseph disease. Journal of Neurology. 248: 717-9. PMID 11569907 DOI: 10.1007/S004150170124 |
0.331 |
|
| 2001 |
Nacmias B, Tedde A, Forleo P, Piacentini S, Guarnieri BM, Bartoli A, Ortenzi L, Petruzzi C, Serio A, Marcon G, Sorbi S. Association between 5-HT(2A) receptor polymorphism and psychotic symptoms in Alzheimer's disease. Biological Psychiatry. 50: 472-5. PMID 11566166 DOI: 10.1016/S0006-3223(01)01114-3 |
0.413 |
|
| 2001 |
Nacmias B, Tedde A, Forleo P, Piacentini S, Latorraca S, Guarnieri BM, Ortenzi L, Bartoli A, Petruzzi C, Serio A, Sorbi S. Psychosis, serotonin receptor polymorphism and Alzheimer's disease. Archives of Gerontology and Geriatrics. Supplement. 7: 279-83. PMID 11431075 DOI: 10.1016/S0167-4943(01)00150-9 |
0.365 |
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| 2001 |
Trippi F, Botto N, Scarpato R, Petrozzi L, Bonuccelli U, Latorraca S, Sorbi S, Migliore L. Spontaneous and induced chromosome damage in somatic cells of sporadic and familial Alzheimer's disease patients. Mutagenesis. 16: 323-7. PMID 11420400 DOI: 10.1093/Mutage/16.4.323 |
0.434 |
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| 2001 |
Carrieri G, Bonafè M, De Luca M, Rose G, Varcasia O, Bruni A, Maletta R, Nacmias B, Sorbi S, Corsonello F, Feraco E, Andreev KF, Yashin AI, Franceschi C, De Benedictis G. Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease. Human Genetics. 108: 194-8. PMID 11354629 DOI: 10.1007/S004390100463 |
0.403 |
|
| 2001 |
Nacmias B, Tedde A, Cellini E, Forleo P, Orlacchio A, Guarnieri BM, Petruzzi C, D'Andrea F, Serio A, Sorbi S. Alpha2-macroglobulin polymorphisms in Italian sporadic and familial Alzheimer's disease. Neuroscience Letters. 299: 9-12. PMID 11166925 DOI: 10.1016/S0304-3940(00)01758-4 |
0.438 |
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| 2000 |
Sorbi S, Alberoni M, Alfieri P, Amici S, Antana D, Appollonio I, Avanzi S, Bartoli A, Bergamasco B, Bracco L, Bruni A, Bugiani O, Caffarra P, Caltagirone C, Carolei A, et al. Guidelines for the diagnosis of dementia and Alzheimer's disease Neurological Sciences. 21: 187-194. PMID 11214656 DOI: 10.1007/S100720070075 |
0.344 |
|
| 2000 |
Ballerini C, Campani D, Rombolà G, Gran B, Nacmias B, Amato MP, Siracusa G, Bartolozzi L, Sorbi S, Massacesi L. Association of apolipoprotein E polymorphism to clinical heterogeneity of multiple sclerosis. Neuroscience Letters. 296: 174-6. PMID 11109009 DOI: 10.1016/S0304-3940(00)01646-3 |
0.324 |
|
| 2000 |
Balestrieri M, Nacmias B, Sorbi S, Marcon G. Are premorbid personality traits linked to the risk of Alzheimer's Disease? A case series of subjects with familial mutation. Psychotherapy and Psychosomatics. 69: 335-8. PMID 11070447 DOI: 10.1159/000012417 |
0.407 |
|
| 2000 |
Gestri D, Cecchi C, Tedde A, Latorraca S, Orlacchio A, Grassi E, Massaro AM, Liguri G, St George-Hyslop PH, Sorbi S. Lack of SOD1 gene mutations and activity alterations in two Italian families with amyotrophic lateral sclerosis. Neuroscience Letters. 289: 157-60. PMID 10961653 DOI: 10.1016/S0304-3940(00)01273-8 |
0.321 |
|
| 2000 |
Murphy EJ, Zhang H, Sorbi S, Rapoport SI, Gibson GE. Phospholipid composition and levels are not altered in fibroblasts bearing presenilin-1 mutations. Brain Research Bulletin. 52: 207-12. PMID 10822162 DOI: 10.1016/S0361-9230(00)00257-4 |
0.37 |
|
| 2000 |
Sorbi S, Forleo P, Fani C, Piacentini S. Double-blind, crossover, placebo-controlled clinical trial with L-acetylcarnitine in patients with degenerative cerebellar ataxia. Clinical Neuropharmacology. 23: 114-8. PMID 10803803 DOI: 10.1097/00002826-200003000-00010 |
0.317 |
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| 2000 |
Orlacchio A, Kawarai T, Massaro AM, St George-Hyslop PH, Sorbi S. Absence of linkage between familial amyotrophic lateral sclerosis and copper chaperone for the superoxide dismutase gene locus in two Italian pedigrees. Neuroscience Letters. 285: 83-6. PMID 10793232 DOI: 10.1016/S0304-3940(00)01032-6 |
0.307 |
|
| 2000 |
Farrer LA, Sherbatich T, Keryanov SA, Korovaitseva GI, Rogaeva EA, Petruk S, Premkumar S, Moliaka Y, Song YQ, Pei Y, Sato C, Selezneva ND, Voskresenskaya S, Golimbet V, Sorbi S, et al. Association between angiotensin-converting enzyme and Alzheimer disease. Archives of Neurology. 57: 210-4. PMID 10681079 DOI: 10.1001/Archneur.57.2.210 |
0.38 |
|
| 2000 |
Forleo P, Tedde A, Nacmias B, Marcon G, Orlacchio A, Sorbi S. Angiotensin converting enzyme gene polymorphism in presenilin linked Alzheimer's disease families and sporadic acid Neurobiology of Aging. 21: 46. DOI: 10.1016/S0197-4580(00)82884-5 |
0.369 |
|
| 2000 |
Orlacchio A, Tedde A, Firenze U, Parnetti L, Perugia U, George-Hyslop PHS, Sorbi S, Emialiani C. Alfa-D-mannosidases in patients with familial Alzheimer's disease Neurobiology of Aging. 21: 16. DOI: 10.1016/S0197-4580(00)82748-7 |
0.369 |
|
| 2000 |
Nacmias B, Tedde A, Cellini E, Forleo P, Orlacchio A, Petruzzi C, Guarnieri BM, Sorbi S. No association between α2-macroglobulin DNA polymorphism and Italian sporadic Alzheimer's disease Neurobiology of Aging. 21: 104. DOI: 10.1016/S0197-4580(00)82265-4 |
0.352 |
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| 2000 |
Grimaldi LME, Casadei VM, Ferri C, Veglia F, Licastro F, Annoni G, Biunno I, Bellis GD, Sorbi S, Mariani C, Canal N, Griffin WST, Franceschi M. Association of early-onset Alzheimer's disease with an interleukin-1α gene polymorphism Annals of Neurology. 47: 361-365. DOI: 10.1002/1531-8249(200003)47:3<361::Aid-Ana12>3.0.Co;2-N |
0.318 |
|
| 1999 |
Nacmias B, Ricca V, Tedde A, Mezzani B, Rotella CM, Sorbi S. 5-HT2A receptor gene polymorphisms in anorexia nervosa and bulimia nervosa. Neuroscience Letters. 277: 134-6. PMID 10624828 DOI: 10.1016/S0304-3940(99)00859-9 |
0.318 |
|
| 1999 |
Cecchi C, Latorraca S, Sorbi S, Iantomasi T, Favilli F, Vincenzini MT, Liguri G. Gluthatione level is altered in lymphoblasts from patients with familial Alzheimer's disease. Neuroscience Letters. 275: 152-4. PMID 10568522 DOI: 10.1016/S0304-3940(99)00751-X |
0.411 |
|
| 1999 |
Casadei VM, Ferri C, Veglia F, Gavazzi A, Salani G, Cattaneo M, Sorbi S, Annoni G, Licastro F, Mariani C, Franceschi M, Grimaldi LM. APOE-491 promoter polymorphism is a risk factor for late-onset Alzheimer's disease. Neurology. 53: 1888-9. PMID 10563653 DOI: 10.1212/Wnl.53.8.1888 |
0.44 |
|
| 1999 |
Brandi ML, Becherini L, Gennari L, Racchi M, Bianchetti A, Nacmias B, Sorbi S, Mecocci P, Senin U, Govoni S. Association of the estrogen receptor alpha gene polymorphisms with sporadic Alzheimer's disease. Biochemical and Biophysical Research Communications. 265: 335-8. PMID 10558867 DOI: 10.1006/Bbrc.1999.1665 |
0.438 |
|
| 1999 |
Rogaeva EA, Premkumar S, Grubber J, Serneels L, Scott WK, Kawarai T, Song Y, Hill DL, Abou-Donia SM, Martin ER, Vance JJ, Yu G, Orlacchio A, Pei Y, Nishimura M, ... ... Sorbi S, et al. An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease. Nature Genetics. 22: 19-22. PMID 10319855 DOI: 10.1038/8729 |
0.404 |
|
| 1999 |
Ballerini C, Nacmias B, Rombolà G, Marcon G, Massacesi L, Sorbi S. HLA A2 allele is associated with age at onset of Alzheimer's disease. Annals of Neurology. 45: 397-400. PMID 10072057 DOI: 10.1002/1531-8249(199903)45:3<397::Aid-Ana18>3.0.Co;2-4 |
0.379 |
|
| 1998 |
Farrer LA, Abraham CR, Haines JL, Rogaeva EA, Song Y, McGraw WT, Brindle N, Premkumar S, Scott WK, Yamaoka LH, Saunders AM, Roses AD, Auerbach SA, Sorbi S, Duara R, et al. Association between bleomycin hydrolase and Alzheimer's disease in caucasians. Annals of Neurology. 44: 808-11. PMID 9818937 DOI: 10.1002/Ana.410440515 |
0.442 |
|
| 1998 |
Rogaeva E, Premkumar S, Song Y, Sorbi S, Brindle N, Paterson A, Duara R, Levesque G, Yu G, Nishimura M, Ikeda M, O'Toole C, Kawarai T, Jorge R, Vilarino D, et al. Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneity. Jama. 280: 614-8. PMID 9718052 DOI: 10.1001/Jama.280.7.614 |
0.376 |
|
| 1998 |
Song YQ, Rogaeva E, Premkumar S, Brindle N, Kawarai T, Orlacchio A, Yu G, Levesque G, Nishimura M, Ikeda M, Pei Y, O'Toole C, Duara R, Barker W, Sorbi S, et al. Absence of association between Alzheimer disease and the -491 regulatory region polymorphism of APOE. Neuroscience Letters. 250: 189-92. PMID 9708864 DOI: 10.1016/S0304-3940(98)00470-4 |
0.411 |
|
| 1998 |
Sorbi S, Nacmias B, Tedde A, Ricca V, Mezzani B, Rotella CM. 5-HT2A promoter polymorphism in anorexia nervosa. Lancet. 351: 1785. PMID 9635955 DOI: 10.1016/S0140-6736(05)78745-6 |
0.33 |
|
| 1998 |
Sorbi S, Nacmias B, Tedde A, Latorraca S, Forleo P, Guarnieri BM, Petruzzi C, Daneluzzo E, Ortenzi L, Piacentini S, Amaducci L. No implication of apolipoprotein E polymorphism in Italian schizophrenic patients. Neuroscience Letters. 244: 118-20. PMID 9572600 DOI: 10.1016/S0304-3940(98)00144-X |
0.429 |
|
| 1998 |
Nacmias B, Marcon G, Tedde A, Forleo P, Latorraca S, Piacentini S, Amaducci L, Sorbi S. Implication of alpha1-antichymotrypsin polymorphism in familial Alzheimer's disease. Neuroscience Letters. 244: 85-8. PMID 9572591 DOI: 10.1016/S0304-3940(98)00134-7 |
0.458 |
|
| 1998 |
Brindle N, Song Y, Rogaeva E, Premkumar S, Levesque G, Yu G, Ikeda M, Nishimura M, Paterson A, Sorbi S, Duara R, Farrer L, St George-Hyslop P. Analysis of the butyrylcholinesterase gene and nearby chromosome 3 markers in Alzheimer disease. Human Molecular Genetics. 7: 933-5. PMID 9536099 DOI: 10.1093/Hmg/7.5.933 |
0.397 |
|
| 1997 |
Blass JP, Sheu KF, Piacentini S, Sorbi S. Inherent abnormalities in oxidative metabolism in Alzheimer's disease: interaction with vascular abnormalities. Annals of the New York Academy of Sciences. 826: 382-5. PMID 9329708 DOI: 10.1111/J.1749-6632.1997.Tb48488.X |
0.346 |
|
| 1997 |
Nacmias B, Tedde A, Guarnieri BM, Petruzzi C, Ortenzi L, Serio A, Amaducci L, Sorbi S. Analysis of apolipoprotein E, alpha1-antichymotrypsin and presenilin-1 genes polymorphisms in dementia caused by normal pressure hydrocephalus in man. Neuroscience Letters. 229: 177-80. PMID 9237487 DOI: 10.1016/S0304-3940(97)00449-7 |
0.438 |
|
| 1997 |
Salvatore M, Seeber AC, Nacmias B, Petraroli R, Sorbi S, Pocchiari M. Alpha1 antichymotrypsin signal peptide polymorphism in sporadic Creutzfeldt-Jakob disease. Neuroscience Letters. 227: 140-2. PMID 9180223 DOI: 10.1016/S0304-3940(97)00308-X |
0.387 |
|
| 1997 |
Sorbi S, Nacmias B, Tedde A, Forleo P, Piacentini S, Latorraca S, Amaducci L. Presenilin-1 gene intronic polymorphism in sporadic and familial Alzheimer's disease. Neuroscience Letters. 222: 132-4. PMID 9111746 DOI: 10.1016/S0304-3940(97)13345-6 |
0.438 |
|
| 1997 |
Perani D, Grassi F, Sorbi S, Nacmias B, Piacentini S, Piersanti P, Provinciali L, Amaducci L, Fazio F. PET study in subjects from two Italian FAD families with APP717 Val to Ileu mutation European Journal of Neurology. 4: 214-220. DOI: 10.1111/J.1468-1331.1997.Tb00337.X |
0.36 |
|
| 1996 |
Nacmias B, Tedde A, Latorraca S, Piacentini S, Bracco L, Amaducci L, Guarnieri BM, Petruzzi C, Ortenzi L, Sorbi S. Apolipoprotein E and alpha1-antichymotrypsin polymorphism in Alzheimer's disease. Annals of Neurology. 40: 678-80. PMID 8871590 DOI: 10.1002/Ana.410400420 |
0.427 |
|
| 1996 |
Sherrington R, Froelich S, Sorbi S, Campion D, Chi H, Rogaeva EA, Levesque G, Rogaev EI, Lin C, Liang Y, Ikeda M, Mar L, Brice A, Agid Y, Percy ME, et al. Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant. Human Molecular Genetics. 5: 985-8. PMID 8817335 DOI: 10.1093/Hmg/5.7.985 |
0.367 |
|
| 1996 |
Liguri G, Cecchi C, Latorraca S, Pieri A, Sorbi S, Degl'Innocenti D, Ramponi G. Alteration of acylphosphatase levels in familial Alzheimer's disease fibroblasts with presenilin gene mutations. Neuroscience Letters. 210: 153-6. PMID 8805118 DOI: 10.1016/0304-3940(96)12696-3 |
0.371 |
|
| 1996 |
Failli P, Tesco G, Ruocco C, Ginestroni A, Amaducci L, Giotti A, Sorbi S. The effect of tetraethylammonium on intracellular calcium concentration in Alzheimer's disease fibroblasts with APP, S182 and E5-1 missense mutations. Neuroscience Letters. 208: 216-8. PMID 8733308 DOI: 10.1016/0304-3940(96)12586-6 |
0.373 |
|
| 1996 |
Sorbi S, Nacmias B, Forleo P, Piacentini S, Amaducci L. Alzheimer's disease and apolipoprotein E in Italy. Annals of the New York Academy of Sciences. 777: 260-5. PMID 8624095 DOI: 10.1111/J.1749-6632.1996.Tb34429.X |
0.446 |
|
| 1996 |
Latorraca S, Cecchi C, Pieri A, Liguri G, Sorbi S, Ramponi G, Amaducci L. 785 Familial Alzheimer's disease fibroblasts with presenilin genes mutations: Alteration'of Acylphosphatase levels Neurobiology of Aging. 17. DOI: 10.1016/S0197-4580(96)80787-1 |
0.383 |
|
| 1996 |
Nacmias B, Tedde A, Latorraca S, Forleo P, Piacentini S, Sorbi S, Amaducci L. 229 Apolipoprotein E and α1-antichymotrypsin polymorphism in Italian Alzheimer's disease Neurobiology of Aging. 17. DOI: 10.1016/S0197-4580(96)80231-4 |
0.362 |
|
| 1995 |
Salvatore M, Seeber AC, Nacmias B, Petraroli R, D'Alessandro M, Sorbi S, Pocchiari M. Apolipoprotein E in sporadic and familial Creutzfeldt-Jakob disease. Neuroscience Letters. 199: 95-8. PMID 8584252 DOI: 10.1016/0304-3940(95)12030-8 |
0.397 |
|
| 1995 |
Nacmias B, Latorraca S, Piersanti P, Forleo P, Piacentini S, Bracco L, Amaducci L, Sorbi S. ApoE genotype and familial Alzheimer's disease: a possible influence on age of onset in APP717 Val-->Ile mutated families. Neuroscience Letters. 183: 1-3. PMID 7746463 DOI: 10.1016/0304-3940(94)11100-W |
0.407 |
|
| 1995 |
Sorbi S, Piacentini S, Latorraca S, Piersanti P, Amaducci L. Alterations in metabolic properties in fibroblasts in Alzheimer disease. Alzheimer Disease and Associated Disorders. 9: 73-7. PMID 7662326 DOI: 10.1097/00002093-199509020-00003 |
0.346 |
|
| 1995 |
Rogaev EI, Sherrington R, Rogaeva EA, Levesque G, Ikeda M, Liang Y, Chi H, Lin C, Holman K, Tsuda T, Mar L, Sorbi S, Nacmias B, Piacentini S, Amaducci L, et al. Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene Nature. 376: 775-778. PMID 7651536 DOI: 10.1038/376775A0 |
0.389 |
|
| 1995 |
Sorbi S, Nacmias B, Forleo P, Piacentini S, Sherrington R, Rogaev E, St George Hyslop P, Amaducci L. Missense mutation of S182 gene in Italian families with early-onset Alzheimer's disease. Lancet. 346: 439-40. PMID 7623584 DOI: 10.1016/S0140-6736(95)92809-X |
0.383 |
|
| 1995 |
Sorbi S, Nacmias B, Forleo P, Piacentini S, Latorraca S, Amaducci L. Epistatic effect of APP717 mutation and apolipoprotein E genotype in familial Alzheimer's disease. Annals of Neurology. 38: 124-7. PMID 7611715 DOI: 10.1002/Ana.410380120 |
0.405 |
|
| 1995 |
Sherrington R, Rogaev EI, Liang Y, Rogaeva EA, Levesque G, Ikeda M, Chi H, Lin C, Li G, Holman K, Tsuda T, Mar L, Foncin JF, Bruni AC, Montesi MP, ... Sorbi S, et al. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease. Nature. 375: 754-60. PMID 7596406 DOI: 10.1038/375754A0 |
0.433 |
|
| 1994 |
Sorbi S, Nacmias B, Mortilla M, Forleo P, Piacentini S, Amaducci L. Molecular genetics of Alzheimer's disease in Italian families. Neurochemistry International. 25: 81-4. PMID 7950975 DOI: 10.1016/0197-0186(94)90057-4 |
0.354 |
|
| 1994 |
Sorbi S, Nacmias B, Forleo P, Latorraca S, Gobbini I, Bracco L, Piacentini S, Amaducci L. ApoE allele frequencies in Italian sporadic and familial Alzheimer's disease. Neuroscience Letters. 177: 100-2. PMID 7824157 DOI: 10.1016/0304-3940(94)90054-X |
0.426 |
|
| 1994 |
Fisher GH, Petrucelli L, Gardner C, Emory C, Frey WH, Amaducci L, Sorbi S, Sorrentino G, Borghi M, D'Aniello A. Free D-amino acids in human cerebrospinal fluid of Alzheimer disease, multiple sclerosis, and healthy control subjects. Molecular and Chemical Neuropathology / Sponsored by the International Society For Neurochemistry and the World Federation of Neurology and Research Groups On Neurochemistry and Cerebrospinal Fluid. 23: 115-24. PMID 7702702 DOI: 10.1007/Bf02815405 |
0.321 |
|
| 1994 |
Nacmias B, Latorraca S, Magnelli L, Falcini M, Bracco L, Piacentini S, Amaducci L, Sorbi S. Apolipoprotein E polymorphism in italian early onset familial and sporadic Alzheimer's disease Neurobiology of Aging. 15. DOI: 10.1016/0197-4580(94)92997-1 |
0.402 |
|
| 1993 |
Sorbi S, Nacmias B, Forleo P, Piacentini S, Amaducci L, Provinciali L. APP717 and Alzheimer's disease in Italy. Nature Genetics. 4: 10. PMID 8513318 DOI: 10.1038/Ng0593-10 |
0.386 |
|
| 1993 |
Tesco G, Vergelli M, Amaducci L, Sorbi S. Growth properties of familial Alzheimer skin fibroblasts during in vitro aging. Experimental Gerontology. 28: 51-8. PMID 8436204 DOI: 10.1016/0531-5565(93)90019-A |
0.326 |
|
| 1993 |
Taddei N, Liguri G, Sorbi S, Amaducci L, Camici G, Nassi P, Cecchi C, Ramponi G. Cerebral soluble ubiquitin is increased in patients with Alzheimer's disease. Neuroscience Letters. 151: 158-61. PMID 8389435 DOI: 10.1016/0304-3940(93)90010-I |
0.387 |
|
| 1993 |
Rogaev EI, Lukiw WJ, Vaula G, Haines JL, Rogaeva EA, Tsuda T, Alexandrova N, Liang Y, Mortilla M, Amaducci L, Bergamini L, Bruni AC, Foncin JF, Macciardi F, Montesi M, ... Sorbi S, et al. Analysis of the c-FOS gene on chromosome 14 and the promoter of the amyloid precursor protein gene in familial Alzheimer's disease. Neurology. 43: 2275-9. PMID 8232942 DOI: 10.1212/Wnl.43.11.2275 |
0.324 |
|
| 1993 |
Sorbi S. Molecular genetics of Alzheimer's disease. Aging (Milan, Italy). 5: 417-25. PMID 8161573 DOI: 10.1007/Bf03324196 |
0.395 |
|
| 1992 |
Tesco G, Latorraca S, Piersanti P, Sorbi S, Piacentini S, Amaducci L. Free radical injury in skin cultured fibroblasts from Alzheimer's disease patients. Annals of the New York Academy of Sciences. 673: 149-53. PMID 1485712 DOI: 10.1111/J.1749-6632.1992.Tb27446.X |
0.341 |
|
| 1992 |
Vaula G, Mortilla M, Tupler R, Lukiw W, Tanzi R, Nee L, Polinsky R, Foncin J-, Bruni AC, Montesi MP, Sorbi S, George-Hyslop PS. A novel but non-pathogenic mutation in exon 4 of the human amyloid precursor protein (APP) gene. Neuroscience Letters. 144: 46-48. PMID 1436713 DOI: 10.1016/0304-3940(92)90712-G |
0.34 |
|
| 1992 |
Tesco G, Latorraca S, Piersanti P, Piacentini S, Amaducci L, Sorbi S. Alzheimer skin fibroblasts show increased susceptibility to free radicals. Mechanisms of Ageing and Development. 66: 117-20. PMID 1365838 DOI: 10.1016/0047-6374(92)90129-2 |
0.345 |
|
| 1992 |
St George-Hyslop P, Haines J, Rogaev E, Mortilla M, Vaula G, Pericak-Vance M, Foncin JF, Montesi M, Bruni A, Sorbi S, Rainero I, Pinessi L, Pollen D, Polinsky R, Nee L, et al. Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14. Nature Genetics. 2: 330-4. PMID 1303289 DOI: 10.1038/Ng1292-330 |
0.366 |
|
| 1992 |
Amaducci L, Latorraca S, Piersanti S, Tesco G, Piacentini S, Sorbi S. Biological markers in Alzheimer's disease Neurochemistry International. 21. DOI: 10.1016/0197-0186(92)90013-H |
0.381 |
|
| 1991 |
Amaducci L, Crook TH, Lippi A, Bracco L, Baldereschi M, Latorraca S, Piersanti P, Tesco G, Sorbi S. Use of phosphatidylserine in Alzheimer's disease. Annals of the New York Academy of Sciences. 640: 245-9. PMID 1776745 DOI: 10.1111/J.1749-6632.1991.Tb00227.X |
0.373 |
|
| 1991 |
Amaducci L, Sorbi S, Piacentini S, Bick KL. The first Alzheimer disease case: a metachromatic leukodystrophy? Developmental Neuroscience. 13: 186-7. PMID 1726217 DOI: 10.1159/000112158 |
0.317 |
|
| 1990 |
St George-Hyslop PH, Haines JL, Farrer LA, Polinsky R, Van Broeckhoven C, Goate A, McLachlan DR, Orr H, Bruni AC, Sorbi S, Rainero I, Foncin JF, Pollen D, Cantu JM, Tupler R, et al. Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder. Nature. 347: 194-7. PMID 2395471 DOI: 10.1038/347194A0 |
0.407 |
|
| 1990 |
Paoletti F, Mocali A, Marchi M, Sorbi S, Piacentini S. Occurrence of transketolase abnormalities in extracts of foreskin fibroblasts from patients with Alzheimer's disease. Biochemical and Biophysical Research Communications. 172: 396-401. PMID 2241941 DOI: 10.1016/0006-291X(90)90686-H |
0.373 |
|
| 1990 |
Liguri G, Taddei N, Nassi P, Latorraca S, Nediani C, Sorbi S. Changes in Na+,K(+)-ATPase, Ca2(+)-ATPase and some soluble enzymes related to energy metabolism in brains of patients with Alzheimer's disease. Neuroscience Letters. 112: 338-42. PMID 2163043 DOI: 10.1016/0304-3940(90)90227-Z |
0.317 |
|
| 1990 |
Sorbi S, Mortilla M, Piacentini S, Tonini S, Amaducci L. Altered hexokinase activity in skin cultured fibroblasts and leukocytes from Alzheimer's disease patients. Neuroscience Letters. 117: 165-8. PMID 2149746 DOI: 10.1016/0304-3940(90)90138-Y |
0.406 |
|
| 1990 |
Duyckaerts C, Delaère P, Hauw JJ, Abbamondi-Pinto AL, Sorbi S, Allen I, Brion JP, Flament-Durand J, Duchen L, Kauss J. Rating of the lesions in senile dementia of the Alzheimer type: concordance between laboratories. A European multicenter study under the auspices of EURAGE. Journal of the Neurological Sciences. 97: 295-323. PMID 1698217 DOI: 10.1016/0022-510X(90)90226-D |
0.334 |
|
| 1988 |
Rocca WA, Sorbi S, Pepeu G, Amaducci L. Research on Alzheimer disease in Italy: present and prospects. Alzheimer Disease and Associated Disorders. 2: 123-32. PMID 3063298 DOI: 10.1097/00002093-198802020-00005 |
0.355 |
|
| 1986 |
Sorbi S, Fani C, Piacentini S, Giannini E, Amaducci L. Energy metabolism in demented brain. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 10: 591-7. PMID 3541053 DOI: 10.1016/0278-5846(86)90029-1 |
0.307 |
|
| 1983 |
Sorbi S, Bird ED, Blass JP. Decreased pyruvate dehydrogenase complex activity in Huntington and Alzheimer brain. Annals of Neurology. 13: 72-8. PMID 6219611 DOI: 10.1002/Ana.410130116 |
0.368 |
|
| 1982 |
Sorbi S, Blass JP. Abnormal activation of pyruvate dehydrogenase in Leigh disease fibroblasts. Neurology. 32: 555-8. PMID 7200213 DOI: 10.1212/Wnl.32.5.555 |
0.34 |
|
| 1979 |
Sorbi S, Antuono P, Amaducci L. Choline acetyltransferase and acetylcholinesterase abnormalities in senile dementia: Importance of biochemical measurements in human post-mortem brain specimens Italian Journal of Neurological Sciences. 1: 75-83. PMID 7040296 DOI: 10.1007/Bf02336848 |
0.349 |
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