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Piero Parchi, MD - Publications

Affiliations: 
Neurology Università di Bologna, Bologna, Italy 
Area:
Prion
Website:
http://www.neuroprion.org/en/part_21.html

212 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Zucchi E, Bonetto V, Sorarù G, Martinelli I, Parchi P, Liguori R, Mandrioli J. Neurofilaments in motor neuron disorders: towards promising diagnostic and prognostic biomarkers. Molecular Neurodegeneration. 15: 58. PMID 33059698 DOI: 10.1186/s13024-020-00406-3  0.4
2020 Jones E, Hummerich H, Viré E, Uphill J, Dimitriadis A, Speedy H, Campbell T, Norsworthy P, Quinn L, Whitfield J, Linehan J, Jaunmuktane Z, Brandner S, Jat P, Nihat A, ... ... Parchi P, et al. Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study. The Lancet. Neurology. 19: 840-848. PMID 32949544 DOI: 10.1016/S1474-4422(20)30273-8  0.96
2020 Abu-Rumeileh S, Baiardi S, Ladogana A, Zenesini C, Bartoletti-Stella A, Poleggi A, Mammana A, Polischi B, Pocchiari M, Capellari S, Parchi P. Comparison between plasma and cerebrospinal fluid biomarkers for the early diagnosis and association with survival in prion disease. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 32928934 DOI: 10.1136/jnnp-2020-323826  0.96
2020 Candelise N, Baiardi S, Franceschini A, Rossi M, Parchi P. Towards an improved early diagnosis of neurodegenerative diseases: the emerging role of in vitro conversion assays for protein amyloids. Acta Neuropathologica Communications. 8: 117. PMID 32711575 DOI: 10.1186/s40478-020-00990-x  0.6
2020 Rossi M, Candelise N, Baiardi S, Capellari S, Giannini G, Orrù CD, Antelmi E, Mammana A, Hughson AG, Calandra-Buonaura G, Ladogana A, Plazzi G, Cortelli P, Caughey B, Parchi P. Correction to: Ultrasensitive RT-QuIC assay with high sensitivity and specificity for Lewy body-associated synucleinopathies. Acta Neuropathologica. PMID 32556961 DOI: 10.1007/s00401-020-02170-6  0.96
2020 Bartoletti-Stella A, De Pasqua S, Baiardi S, Bartolomei I, Mengozzi G, Orio G, Pastorelli F, Piras S, Poda R, Raggi A, Maserati MS, Tarozzi M, Liguori R, Salvi F, Parchi P, et al. Characterization of novel progranulin gene variants in Italian patients with neurodegenerative diseases. Neurobiology of Aging. PMID 32507413 DOI: 10.1016/j.neurobiolaging.2020.05.004  0.96
2020 Melis M, Molari A, Floris G, Vascellari S, Balestrino L, Ladogana A, Poleggi A, Parchi P, Cossu G, Melis M, Orrù S, Defazio G. Genetic Creutzfeldt-Jakob disease in Sardinia: a case series linked to the PRNP R208H mutation due to a single founder effect. Neurogenetics. PMID 32458274 DOI: 10.1007/s10048-020-00618-1  0.72
2020 Mantovani P, Riccioli LA, Giannini G, Milletti D, Sorenson TJ, Maserati MS, Oppi F, Elder BD, Cevoli S, Cortelli P, Palandri G, Agati R, Calandra-Buonaura G, Capellari S, ... ... Parchi P, et al. Anterior callosal angle: a new marker of idiopathic normal pressure hydrocephalus? World Neurosurgery. PMID 32348895 DOI: 10.1016/j.wneu.2020.04.085  0.96
2020 Rossi M, Candelise N, Baiardi S, Capellari S, Giannini G, Orrù CD, Antelmi E, Mammana A, Hughson AG, Calandra-Buonaura G, Ladogana A, Plazzi G, Cortelli P, Caughey B, Parchi P. Ultrasensitive RT-QuIC assay with high sensitivity and specificity for Lewy body-associated synucleinopathies. Acta Neuropathologica. PMID 32342188 DOI: 10.1007/s00401-020-02160-8  0.96
2020 Raggi A, Bartoletti-Stella A, Parchi P, Capellari S. First case of an gene mutation causing frontotemporal dementia preceded by adult onset psychiatric symptoms. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-3. PMID 32290710 DOI: 10.1080/21678421.2020.1752251  0.96
2020 Baiardi S, Rizzi R, Capellari S, Bartoletti-Stella A, Zangrandi A, Gasparini F, Ghidoni E, Parchi P. Gerstmann-Sträussler-Scheinker disease ( p.D202N) presenting with atypical parkinsonism. Neurology. Genetics. 6: e400. PMID 32274419 DOI: 10.1212/NXG.0000000000000400  0.96
2020 Calandra-Buonaura G, Sambati L, Baschieri F, Vitiello M, Contin M, Tonon C, Capellari S, Provini F, Cortelli P. The Bologna motor and non-motor prospective study on parkinsonism at onset (BoProPark): study design and population. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. PMID 32219591 DOI: 10.1007/s10072-020-04305-9  0.32
2020 Abu-Rumeileh S, Oeckl P, Baiardi S, Halbgebauer S, Steinacker P, Capellari S, Otto M, Parchi P. CSF Ubiquitin Levels Are Higher in Alzheimer's Disease than in Frontotemporal Dementia and Reflect the Molecular Subtype in Prion Disease. Biomolecules. 10. PMID 32218217 DOI: 10.3390/biom10040497  0.96
2020 Mammana A, Baiardi S, Rossi M, Franceschini A, Donadio V, Capellari S, Caughey B, Parchi P. Detection of prions in skin punch biopsies of Creutzfeldt-Jakob disease patients. Annals of Clinical and Translational Neurology. PMID 32141717 DOI: 10.1002/acn3.51000  0.96
2020 Abu-Rumeileh S, Vacchiano V, Zenesini C, Polischi B, de Pasqua S, Fileccia E, Mammana A, Di Stasi V, Capellari S, Salvi F, Liguori R, Parchi P. Diagnostic-prognostic value and electrophysiological correlates of CSF biomarkers of neurodegeneration and neuroinflammation in amyotrophic lateral sclerosis. Journal of Neurology. PMID 32100123 DOI: 10.1007/s00415-020-09761-z  0.96
2020 Abu-Rumeileh S, Halbgebauer S, Steinacker P, Anderl-Straub S, Polischi B, Ludolph AC, Capellari S, Parchi P, Otto M. CSF SerpinA1 in Creutzfeldt-Jakob disease and frontotemporal lobar degeneration. Annals of Clinical and Translational Neurology. PMID 31957347 DOI: 10.1002/acn3.50980  0.96
2019 Takeuchi A, Mohri S, Kai H, Tamaoka A, Kobayashi A, Mizusawa H, Iwasaki Y, Yoshida M, Shimizu H, Murayama S, Kuroda S, Morita M, Parchi P, Kitamoto T. Two distinct prions in fatal familial insomnia and its sporadic form. Brain Communications. 1: fcz045. PMID 32954274 DOI: 10.1093/braincomms/fcz045  0.36
2019 Abu-Rumeileh S, Steinacker P, Polischi B, Mammana A, Bartoletti-Stella A, Oeckl P, Baiardi S, Zenesini C, Huss A, Cortelli P, Capellari S, Otto M, Parchi P. CSF biomarkers of neuroinflammation in distinct forms and subtypes of neurodegenerative dementia. Alzheimer's Research & Therapy. 12: 2. PMID 31892365 DOI: 10.1186/s13195-019-0562-4  0.96
2019 Saijo E, Metrick MA, Koga S, Parchi P, Litvan I, Spina S, Boxer A, Rojas JC, Galasko D, Kraus A, Rossi M, Newell K, Zanusso G, Grinberg LT, Seeley WW, et al. Correction to: 4-Repeat tau seeds and templating subtypes as brain and CSF biomarkers of frontotemporal lobar degeneration. Acta Neuropathologica. PMID 31748840 DOI: 10.1007/s00401-019-02092-y  0.56
2019 Saijo E, Metrick MA, Koga S, Parchi P, Litvan I, Spina S, Boxer A, Rojas JC, Galasko D, Kraus A, Rossi M, Newell K, Zanusso G, Grinberg LT, Seeley WW, et al. 4-Repeat tau seeds and templating subtypes as brain and CSF biomarkers of frontotemporal lobar degeneration. Acta Neuropathologica. PMID 31616982 DOI: 10.1007/s00401-019-02080-2  0.56
2019 Bongianni M, Ladogana A, Capaldi S, Klotz S, Baiardi S, Cagnin A, Perra D, Fiorini M, Poleggi A, Legname G, Cattaruzza T, Janes F, Tabaton M, Ghetti B, Monaco S, ... ... Parchi P, et al. α-Synuclein RT-QuIC assay in cerebrospinal fluid of patients with dementia with Lewy bodies. Annals of Clinical and Translational Neurology. PMID 31599499 DOI: 10.1002/acn3.50897  0.96
2019 Puopolo M, Catelan D, Capellari S, Ladogana A, Sanguedolce A, Fedele A, Aprile V, Turco GL, Colaizzo E, Tiple D, Vaianella L, Parchi P, Biggeri A, Pocchiari M. Spatial Epidemiology of Sporadic Creutzfeldt-Jakob Disease in Apulia, Italy. Neuroepidemiology. 1-7. PMID 31563913 DOI: 10.1159/000503234  0.96
2019 Minikel EV, Kuhn E, Cocco AR, Vallabh SM, Hartigan CR, Reidenbach AG, Safar JG, Raymond GJ, McCarthy MD, O'Keefe R, Llorens F, Zerr I, Capellari S, Parchi P, Schreiber SL, et al. -Domain-specific quantification of prion protein in cerebrospinal fluid by targeted mass spectrometry. Molecular & Cellular Proteomics : McP. PMID 31558565 DOI: 10.1074/mcp.RA119.001702  0.96
2019 Areškevičiūtė A, Broholm H, Melchior LC, Bartoletti-Stella A, Parchi P, Capellari S, Scheie D, Lund EL. Molecular Characterization of the Danish Prion Diseases Cohort With Special Emphasis on Rare and Unique Cases. Journal of Neuropathology and Experimental Neurology. PMID 31553446 DOI: 10.1093/jnen/nlz089  0.96
2019 Baiardi S, Pizza F, Polischi B, Moresco M, Abu-Rumeileh S, Plazzi G, Parchi P. Cerebrospinal fluid biomarkers of neurodegeneration in narcolepsy type 1. Sleep. PMID 31552425 DOI: 10.1093/sleep/zsz215  0.76
2019 Abu-Rumeileh S, Baiardi S, Polischi B, Mammana A, Franceschini A, Green A, Capellari S, Parchi P. Diagnostic value of surrogate CSF biomarkers for Creutzfeldt-Jakob disease in the era of RT-QuIC. Journal of Neurology. PMID 31541342 DOI: 10.1007/s00415-019-09537-0  0.96
2019 Minikel EV, Vallabh SM, Orseth MC, Brandel JP, Haïk S, Laplanche JL, Zerr I, Parchi P, Capellari S, Safar J, Kenny J, Fong JC, Takada LT, Ponto C, Hermann P, et al. Age at onset in genetic prion disease and the design of preventive clinical trials. Neurology. PMID 31171647 DOI: 10.1212/WNL.0000000000007745  0.96
2019 Areškevičiūtė A, Høgh P, Bartoletti-Stella A, Melchior LC, Nielsen PR, Parchi P, Capellari S, Broholm H, Scheie D, Lund EL. A Novel Eight Octapeptide Repeat Insertion in PRNP Causing Prion Disease in a Danish Family. Journal of Neuropathology and Experimental Neurology. PMID 31107536 DOI: 10.1093/jnen/nlz037  0.96
2019 Mitolo M, Stanzani-Maserati M, Capellari S, Testa C, Rucci P, Poda R, Oppi F, Gallassi R, Sambati L, Rizzo G, Parchi P, Evangelisti S, Talozzi L, Tonon C, Lodi R, et al. Predicting conversion from mild cognitive impairment to Alzheimer's disease using brain H-MRS and volumetric changes: A two- year retrospective follow-up study. Neuroimage. Clinical. 23: 101843. PMID 31071594 DOI: 10.1016/j.nicl.2019.101843  0.96
2019 Rossi M, Kai H, Baiardi S, Bartoletti-Stella A, Carlà B, Zenesini C, Capellari S, Kitamoto T, Parchi P. The characterization of AD/PART co-pathology in CJD suggests independent pathogenic mechanisms and no cross-seeding between misfolded Aβ and prion proteins. Acta Neuropathologica Communications. 7: 53. PMID 30961668 DOI: 10.1186/s40478-019-0706-6  0.96
2019 Vallabh SM, Nobuhara CK, Llorens F, Zerr I, Parchi P, Capellari S, Kuhn E, Klickstein J, Safar JG, Nery FC, Swoboda KJ, Geschwind MD, Zetterberg H, Arnold SE, Minikel EV, et al. Prion protein quantification in human cerebrospinal fluid as a tool for prion disease drug development. Proceedings of the National Academy of Sciences of the United States of America. PMID 30936307 DOI: 10.1073/pnas.1901947116  0.96
2019 Rossi M, Baiardi S, Parchi P. Understanding Prion Strains: Evidence from Studies of the Disease Forms Affecting Humans. Viruses. 11. PMID 30934971 DOI: 10.3390/v11040309  0.6
2019 Tiple D, Poleggi A, Mellina V, Morocutti A, Brusa L, Iani C, Colaizzo E, Vaianella L, Baiardi S, Ladogana A, Parchi P, Pocchiari M. Clinicopathological features of the rare form of Creutzfeldt-Jakob disease in R208H-V129V PRNP carrier. Acta Neuropathologica Communications. 7: 47. PMID 30898147 DOI: 10.1186/s40478-019-0699-1  0.72
2019 Abu-Rumeileh S, Giannini G, Polischi B, Albini-Riccioli L, Milletti D, Oppi F, Stanzani-Maserati M, Capellari S, Mantovani P, Palandri G, Cortelli P, Cevoli S, Parchi P. Revisiting the Cerebrospinal Fluid Biomarker Profile in Idiopathic Normal Pressure Hydrocephalus: The Bologna Pro-Hydro Study. Journal of Alzheimer's Disease : Jad. PMID 30883350 DOI: 10.3233/JAD-181012  0.96
2019 Baiardi S, Abu-Rumeileh S, Rossi M, Zenesini C, Bartoletti-Stella A, Polischi B, Capellari S, Parchi P. Antemortem CSF A42/A40 ratio predicts Alzheimer's disease pathology better than A42 in rapidly progressive dementias. Annals of Clinical and Translational Neurology. 6: 263-273. PMID 30847359 DOI: 10.1002/acn3.697  0.96
2019 Rizzi R, Fisicaro F, Zangrandi A, Ghidoni E, Baiardi S, Ragazzi M, Parchi P. Sudden cardiac death in a patient with LGI1 antibody-associated encephalitis. Seizure. 65: 148-150. PMID 30708290 DOI: 10.1016/j.seizure.2019.01.013  0.6
2019 Nonno R, Notari S, Di Bari MA, Cali I, Pirisinu L, d'Agostino C, Cracco L, Kofskey D, Vanni I, Lavrich J, Parchi P, Agrimi U, Gambetti P. Variable Protease-Sensitive Prionopathy Transmission to Bank Voles. Emerging Infectious Diseases. 25: 73-81. PMID 30561322 DOI: 10.3201/eid2501.180807  0.96
2018 Baiardi S, Rossi M, Capellari S, Parchi P. Recent advances in the histo-molecular pathology of human prion disease. Brain Pathology (Zurich, Switzerland). PMID 30588685 DOI: 10.1111/bpa.12695  0.96
2018 Bartoletti-Stella A, Corrado P, Mometto N, Baiardi S, Durrenberger PF, Arzberger T, Reynolds R, Kretzschmar H, Capellari S, Parchi P. Analysis of RNA Expression Profiles Identifies Dysregulated Vesicle Trafficking Pathways in Creutzfeldt-Jakob Disease. Molecular Neurobiology. PMID 30446946 DOI: 10.1007/s12035-018-1421-1  0.96
2018 Baiardi S, Redaelli V, Ripellino P, Rossi M, Franceschini A, Moggio M, Sola P, Ladogana A, Fociani P, Magherini A, Capellari S, Giese A, Caughey B, Caroppo P, Parchi P. Prion-related peripheral neuropathy in sporadic Creutzfeldt-Jakob disease. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 30355606 DOI: 10.1136/jnnp-2018-319221  0.96
2018 Vicente-Pascual M, Rossi M, Gámez J, Lladó A, Valls J, Grau-Rivera O, Ávila Polo R, Llorens F, Zerr I, Ferrer I, Nos C, Parchi P, Sánchez-Valle R, Gelpí E. Variably protease-sensitive prionopathy presenting within ALS/FTD spectrum. Annals of Clinical and Translational Neurology. 5: 1297-1302. PMID 30349865 DOI: 10.1002/acn3.632  0.56
2018 Abu-Rumeileh S, Mometto N, Bartoletti-Stella A, Polischi B, Oppi F, Poda R, Stanzani-Maserati M, Cortelli P, Liguori R, Capellari S, Parchi P. Cerebrospinal Fluid Biomarkers in Patients with Frontotemporal Dementia Spectrum: A Single-Center Study. Journal of Alzheimer's Disease : Jad. PMID 30320576 DOI: 10.3233/JAD-180409  0.96
2018 Abu-Rumeileh S, Baiardi S, D'Angelo R, Dentale N, Fasulo G, Guarino M, Parchi P. Clinical Reasoning: Rapidly progressive dementia in a patient with HIV after an exotic journey. Neurology. 91: e1360-e1364. PMID 30275129 DOI: 10.1212/WNL.0000000000006285  0.76
2018 Abu-Rumeileh S, Redaelli V, Baiardi S, Mackenzie G, Windl O, Ritchie DL, Didato G, Hernandez-Vara J, Rossi M, Capellari S, Imperiale D, Rizzone MG, Belotti A, Sorbi S, Rozemuller AJM, ... ... Parchi P, et al. Sporadic Fatal Insomnia in Europe: Phenotypic features and diagnostic challenges. Annals of Neurology. PMID 30048013 DOI: 10.1002/ana.25300  0.96
2018 Poleggi A, van der Lee S, Capellari S, Puopolo M, Ladogana A, De Pascali E, Lia D, Formato A, Bartoletti-Stella A, Parchi P, van Duijn C, Pocchiari M. Age at onset of genetic (E200K) and sporadic Creutzfeldt-Jakob diseases is modulated by the gene. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 30032116 DOI: 10.1136/jnnp-2018-318756  0.96
2018 Baiardi S, Capellari S, Bartoletti Stella A, Parchi P. Unusual Clinical Presentations Challenging the Early Clinical Diagnosis of Creutzfeldt-Jakob Disease. Journal of Alzheimer's Disease : Jad. PMID 30010123 DOI: 10.3233/JAD-180123  0.96
2018 Capellari S, Baiardi S, Rinaldi R, Bartoletti-Stella A, Graziano C, Piras S, Calandra-Buonaura G, D'Angelo R, Terziotti C, Lodi R, Donadio V, Pironi L, Cortelli P, Parchi P. Two novel truncating mutations broaden the spectrum of prion amyloidosis. Annals of Clinical and Translational Neurology. 5: 777-783. PMID 29928661 DOI: 10.1002/acn3.568  0.96
2018 Quadri M, Mandemakers W, Grochowska MM, Masius R, Geut H, Fabrizio E, Breedveld GJ, Kuipers D, Minneboo M, Vergouw LJM, Carreras Mascaro A, Yonova-Doing E, Simons E, Zhao T, Di Fonzo AB, ... ... Parchi P, et al. LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study. The Lancet. Neurology. PMID 29887161 DOI: 10.1016/S1474-4422(18)30179-0  0.96
2018 Abu-Rumeileh S, Capellari S, Parchi P. Rapidly Progressive Alzheimer's Disease: Contributions to Clinical-Pathological Definition and Diagnosis. Journal of Alzheimer's Disease : Jad. PMID 29710713 DOI: 10.3233/JAD-171181  0.96
2018 Bartoletti-Stella A, Baiardi S, Stanzani-Maserati M, Piras S, Caffarra P, Raggi A, Pantieri R, Baldassari S, Caporali L, Abu-Rumeileh S, Linarello S, Liguori R, Parchi P, Capellari S. Identification of rare genetic variants in Italian patients with dementia by targeted gene sequencing. Neurobiology of Aging. PMID 29525180 DOI: 10.1016/j.neurobiolaging.2018.02.006  0.96
2018 Giannoccaro MP, Bartoletti-Stella A, Piras S, Casalena A, Oppi F, Ambrosetto G, Montagna P, Liguori R, Parchi P, Capellari S. The First Historically Reported Italian Family with FTD/ALS Teaches a Lesson on C9orf72 RE: Clinical Heterogeneity and Oligogenic Inheritance. Journal of Alzheimer's Disease : Jad. 62: 687-697. PMID 29480190 DOI: 10.3233/JAD-170913  0.96
2018 Race B, Williams K, Hughson AG, Jansen C, Parchi P, Rozemuller AJM, Chesebro B. Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion protein. Acta Neuropathologica Communications. 6: 13. PMID 29458424 DOI: 10.1186/s40478-018-0516-2  0.32
2018 Iaccarino L, Presotto L, Bettinardi V, Gianolli L, Roiter I, Capellari S, Parchi P, Cortelli P, Perani D. An in vivo 11C-PK PET study of microglia activation in Fatal Familial Insomnia. Annals of Clinical and Translational Neurology. 5: 11-18. PMID 29376088 DOI: 10.1002/acn3.498  0.96
2018 Abu-Rumeileh S, Capellari S, Stanzani-Maserati M, Polischi B, Martinelli P, Caroppo P, Ladogana A, Parchi P. The CSF neurofilament light signature in rapidly progressive neurodegenerative dementias. Alzheimer's Research & Therapy. 10: 3. PMID 29368621 DOI: 10.1186/s13195-017-0331-1  0.96
2018 Gramegna LL, Pisano A, Testa C, Manners DN, D'Angelo R, Boschetti E, Giancola F, Pironi L, Caporali L, Capristo M, Valentino ML, Plazzi G, Casali C, Dotti MT, Cenacchi G, ... ... Parchi P, et al. Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy. Ajnr. American Journal of Neuroradiology. PMID 29348134 DOI: 10.3174/ajnr.A5507  0.44
2018 Franceschini A, Strammiello R, Capellari S, Giese A, Parchi P. Regional pattern of microgliosis in sporadic Creutzfeldt-Jakob disease in relation to phenotypic variants and disease progression. Neuropathology and Applied Neurobiology. PMID 29345730 DOI: 10.1111/nan.12461  0.96
2018 Cali I, Cohen ML, Haїk S, Parchi P, Giaccone G, Collins SJ, Kofskey D, Wang H, McLean CA, Brandel JP, Privat N, Sazdovitch V, Duyckaerts C, Kitamoto T, Belay ED, et al. Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study. Acta Neuropathologica Communications. 6: 5. PMID 29310723 DOI: 10.1186/s40478-017-0503-z  0.96
2017 Rossi M, Saverioni D, Di Bari M, Baiardi S, Lemstra AW, Pirisinu L, Capellari S, Rozemuller A, Nonno R, Parchi P. Atypical Creutzfeldt-Jakob disease with PrP-amyloid plaques in white matter: molecular characterization and transmission to bank voles show the M1 strain signature. Acta Neuropathologica Communications. 5: 87. PMID 29169405 DOI: 10.1186/s40478-017-0496-7  0.96
2017 Bartoletti-Stella A, Gasparini L, Giacomini C, Corrado P, Terlizzi R, Giorgio E, Magini P, Seri M, Baruzzi A, Parchi P, Brusco A, Cortelli P, Capellari S. Messenger RNA processing is altered in autosomal dominant leukodystrophy. Human Molecular Genetics. 26: 3868. PMID 28934398 DOI: 10.1093/hmg/ddx225  0.96
2017 Franceschini A, Baiardi S, Hughson AG, McKenzie N, Moda F, Rossi M, Capellari S, Green A, Giaccone G, Caughey B, Parchi P. High diagnostic value of second generation CSF RT-QuIC across the wide spectrum of CJD prions. Scientific Reports. 7: 10655. PMID 28878311 DOI: 10.1038/s41598-017-10922-w  0.96
2017 Baiardi S, Magherini A, Capellari S, Redaelli V, Ladogana A, Rossi M, Tagliavini F, Pocchiari M, Giaccone G, Parchi P. Towards an early clinical diagnosis of sporadic CJD VV2 (ataxic type). Journal of Neurology, Neurosurgery, and Psychiatry. PMID 28668775 DOI: 10.1136/jnnp-2017-315942  0.96
2017 Giannoccaro MP, Bartoletti-Stella A, Piras S, Pession A, De Massis P, Oppi F, Stanzani-Maserati M, Pasini E, Baiardi S, Avoni P, Parchi P, Liguori R, Capellari S. Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature. Journal of Neurology. PMID 28620717 DOI: 10.1007/s00415-017-8540-x  0.96
2017 Baschieri F, Calandra-Buonaura G, Cecere A, Barletta G, Contin M, Parchi P, Cortelli P. Iodine-123-meta-iodobenzylguanidine Myocardial Scintigraphy in Isolated Autonomic Failure: Potential Red Flag for Future Multiple System Atrophy. Frontiers in Neurology. 8: 225. PMID 28603516 DOI: 10.3389/fneur.2017.00225  0.36
2017 Terlizzi R, Valentino ML, Bartoletti-Stella A, Columbaro M, Piras S, Stanzani-Maserati M, Quadri M, Breedveld GJ, Bonifati V, Martinelli P, Parchi P, Capellari S. Muscle ceroid lipofuscin-like deposits in a patient with corticobasal syndrome due to a progranulin mutation. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 28543767 DOI: 10.1002/mds.27049  0.96
2017 Lattanzio F, Abu-Rumeileh S, Franceschini A, Kai H, Amore G, Poggiolini I, Rossi M, Baiardi S, McGuire L, Ladogana A, Pocchiari M, Green A, Capellari S, Parchi P. Prion-specific and surrogate CSF biomarkers in Creutzfeldt-Jakob disease: diagnostic accuracy in relation to molecular subtypes and analysis of neuropathological correlates of p-tau and Aβ42 levels. Acta Neuropathologica. PMID 28205010 DOI: 10.1007/s00401-017-1683-0  0.96
2016 Rumeileh SA, Lattanzio F, Maserati MS, Rizzi R, Capellari S, Parchi P. Diagnostic Accuracy of a Combined Analysis of Cerebrospinal Fluid t-PrP, t-tau, p-tau, and Aβ42 in the Differential Diagnosis of Creutzfeldt-Jakob Disease from Alzheimer's Disease with Emphasis on Atypical Disease Variants. Journal of Alzheimer's Disease : Jad. PMID 27886009 DOI: 10.3233/JAD-160740  0.96
2016 Vita MG, Tiple D, Bizzarro A, Ladogana A, Colaizzo E, Capellari S, Rossi M, Parchi P, Masullo C, Pocchiari M. Patient with rapidly evolving neurological disease with neuropathological lesions of Creutzfeldt-Jakob disease, Lewy body dementia, chronic subcortical vascular encephalopathy and meningothelial meningioma. Neuropathology : Official Journal of the Japanese Society of Neuropathology. PMID 27634418 DOI: 10.1111/neup.12343  0.96
2016 McGuire LI, Poleggi A, Poggiolini I, Suardi S, Grznarova K, Shi S, de Vil B, Sarros S, Satoh K, Cheng K, Cramm M, Fairfoul G, Schmitz M, Zerr I, Cras P, ... ... Parchi P, et al. CSF RT-QuIC is a robust and reliable test for sporadic CJD: An international study. Annals of Neurology. PMID 27130376 DOI: 10.1002/ana.24679  0.72
2016 Cescatti M, Saverioni D, Capellari S, Tagliavini F, Kitamoto T, Ironside J, Giese A, Parchi P. Analysis of conformational stability of abnormal prion protein aggregates across the spectrum of Creutzfeldt-Jakob disease prions. Journal of Virology. PMID 27122583 DOI: 10.1128/JVI.00144-16  0.96
2016 Takeuchi A, Kobayashi A, Parchi P, Yamada M, Morita M, Uno S, Kitamoto T. Distinctive properties of plaque-type dura mater graft-associated Creutzfeldt-Jakob disease in cell-protein misfolding cyclic amplification. Laboratory Investigation; a Journal of Technical Methods and Pathology. PMID 26878132 DOI: 10.1038/labinvest.2016.27  0.96
2016 Minikel EV, Vallabh SM, Lek M, Estrada K, Samocha KE, Sathirapongsasuti JF, McLean CY, Tung JY, Yu LP, Gambetti P, Blevins J, Zhang S, Cohen Y, Chen W, Yamada M, ... ... Parchi P, et al. Quantifying prion disease penetrance using large population control cohorts. Science Translational Medicine. 8: 322ra9. PMID 26791950 DOI: 10.1126/scitranslmed.aad5169  0.96
2015 Baiardi S, Capellari S, Ladogana A, Strumia S, Santangelo M, Pocchiari M, Parchi P. Revisiting the Heidenhain Variant of Creutzfeldt-Jakob Disease: Evidence for Prion Type Variability Influencing Clinical Course and Laboratory Findings. Journal of Alzheimer's Disease : Jad. PMID 26682685 DOI: 10.3233/JAD-150668  0.96
2015 Kobayashi A, Parchi P, Yamada M, Mohri S, Kitamoto T. Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases. Neuropathology : Official Journal of the Japanese Society of Neuropathology. PMID 26669818 DOI: 10.1111/neup.12270  0.96
2015 Bartoletti-Stella A, Gasparini L, Giacomini C, Corrado P, Terlizzi R, Giorgio E, Magini P, Seri M, Baruzzi A, Parchi P, Brusco A, Cortelli P, Capellari S. Messenger RNA processing is altered in autosomal dominant leukodystrophy. Human Molecular Genetics. 24: 2746-56. PMID 25637521 DOI: 10.1093/hmg/ddv034  0.96
2015 Kobayashi A, Parchi P, Yamada M, Brown P, Saverioni D, Matsuura Y, Takeuchi A, Mohri S, Kitamoto T. Transmission properties of atypical Creutzfeldt-Jakob disease: a clue to disease etiology? Journal of Virology. 89: 3939-46. PMID 25609817 DOI: 10.1128/JVI.03183-14  0.96
2015 Scontrini A, Di Bonaventura C, Fiorelli M, Tiple D, Colaizzo E, Ladogana A, Parchi P, Pocchiari M. Creutzfeldt-Jakob disease masked by head trauma and features of Wilson's disease. The International Journal of Neuroscience. 125: 312-4. PMID 25485669 DOI: 10.3109/00207454.2014.992428  0.96
2015 Alafuzoff I, Pikkarainen M, Neumann M, Arzberger T, Al-Sarraj S, Bodi I, Bogdanovic N, Bugiani O, Ferrer I, Gelpi E, Gentleman S, Giaccone G, Graeber MB, Hortobagyi T, Ince PG, ... ... Parchi P, et al. Erratum to: Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortium. Journal of Neural Transmission (Vienna, Austria : 1996). 122: 973-4. PMID 25418279 DOI: 10.1007/s00702-014-1337-5  0.96
2015 Alafuzoff I, Pikkarainen M, Neumann M, Arzberger T, Al-Sarraj S, Bodi I, Bogdanovic N, Bugiani O, Ferrer I, Gelpi E, Gentleman S, Giaccone G, Graeber MB, Hortobagyi T, Ince PG, ... ... Parchi P, et al. Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortium. Journal of Neural Transmission (Vienna, Austria : 1996). 122: 957-72. PMID 25239189 DOI: 10.1007/s00702-014-1304-1  0.96
2014 Cardone F, Principe S, Schininà ME, Maras B, Capellari S, Parchi P, Notari S, Di Francesco L, Poleggi A, Galeno R, Vinci R, Mellina V, Almonti S, Ladogana A, Pocchiari M. Mutant PrPCJD prevails over wild-type PrPCJD in the brain of V210I and R208H genetic Creutzfeldt-Jakob disease patients. Biochemical and Biophysical Research Communications. 454: 289-94. PMID 25450391 DOI: 10.1016/j.bbrc.2014.10.051  0.96
2014 D'Angelo R, Rinaldi R, Parchi P, Cirignotta F. Wait and see: a 5 year history of 'recurrent dementia'. Bmj Case Reports. 2014. PMID 25410032 DOI: 10.1136/bcr-2014-205991  0.96
2014 Pizza F, Vandi S, Liguori R, Parchi P, Avoni P, Mignot E, Plazzi G. Primary progressive narcolepsy type 1: the other side of the coin. Neurology. 83: 2189-90. PMID 25355832 DOI: 10.1212/WNL.0000000000001051  0.96
2014 Damato V, Cuccagna C, Costantini EM, Gaudino S, Colosimo C, Parchi P, Servidei S, Luigetti M. Creutzfeldt-Jakob disease manifesting as stroke mimic in a 78-year-old patient: pitfalls and tips in the diagnosis. Journal of the Neurological Sciences. 346: 343-4. PMID 25201717 DOI: 10.1016/j.jns.2014.08.026  0.96
2014 Bacchelli E, Ceroni F, Pinto D, Lomartire S, Giannandrea M, D'Adamo P, Bonora E, Parchi P, Tancredi R, Battaglia A, Maestrini E. A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder. Journal of Neurodevelopmental Disorders. 6: 17. PMID 25050139 DOI: 10.1186/1866-1955-6-17  0.96
2014 Cavallieri F, Mandrioli J, Tondelli M, Vitetta F, Stipa C, Vallone S, Georgoulopoulou E, Barbi F, Liguori R, Parchi P, Nichelli P. Pearls & Oy-sters: rapidly progressive dementia: prions or immunomediated? Neurology. 82: e149-52. PMID 24778290 DOI: 10.1212/WNL.0000000000000354  0.96
2014 Bonora E, Graziano C, Minopoli F, Bacchelli E, Magini P, Diquigiovanni C, Lomartire S, Bianco F, Vargiolu M, Parchi P, Marasco E, Mantovani V, Rampoldi L, Trudu M, Parmeggiani A, et al. Maternally inherited genetic variants of CADPS2 are present in autism spectrum disorders and intellectual disability patients. Embo Molecular Medicine. 6: 795-809. PMID 24737869 DOI: 10.1002/emmm.201303235  0.96
2014 Moghadam KK, Pizza F, La Morgia C, Franceschini C, Tonon C, Lodi R, Barboni P, Seri M, Ferrari S, Liguori R, Donadio V, Parchi P, Cornelio F, Inzitari D, Mignarri A, et al. Narcolepsy is a common phenotype in HSAN IE and ADCA-DN. Brain : a Journal of Neurology. 137: 1643-55. PMID 24727570 DOI: 10.1093/brain/awu069  0.96
2014 Cortelli P, Fabbri M, Calandra-Buonaura G, Capellari S, Tinuper P, Parchi P, Lugaresi E. Gait disorders in fatal familial insomnia. Movement Disorders : Official Journal of the Movement Disorder Society. 29: 420-4. PMID 24375448 DOI: 10.1002/mds.25786  0.96
2013 Poggiolini I, Saverioni D, Parchi P. Prion protein misfolding, strains, and neurotoxicity: an update from studies on Mammalian prions. International Journal of Cell Biology. 2013: 910314. PMID 24454379 DOI: 10.1155/2013/910314  0.96
2013 Vita MG, Gaudino S, Di Giuda D, Sauchelli D, Alboini PE, Gangemi E, Bizzarro A, Scaricamazza E, Capellari S, Parchi P, Masullo C. R208H-129VV haplotype in the prion protein gene: phenotype and neuroimaging of a patient with genetic Creutzfeldt-Jakob disease. Journal of Neurology. 260: 2650-2. PMID 23979103 DOI: 10.1007/s00415-013-7078-9  0.96
2013 Saverioni D, Notari S, Capellari S, Poggiolini I, Giese A, Kretzschmar HA, Parchi P. Analyses of protease resistance and aggregation state of abnormal prion protein across the spectrum of human prions. The Journal of Biological Chemistry. 288: 27972-85. PMID 23897825 DOI: 10.1074/jbc.M113.477547  0.96
2013 Mattsson N, Andreasson U, Persson S, Carrillo MC, Collins S, Chalbot S, Cutler N, Dufour-Rainfray D, Fagan AM, Heegaard NH, Robin Hsiung GY, Hyman B, Iqbal K, Kaeser SA, Käser SA, ... ... Parchi P, et al. CSF biomarker variability in the Alzheimer's Association quality control program. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. 9: 251-61. PMID 23622690 DOI: 10.1016/j.jalz.2013.01.010  0.96
2013 Parchi P, Capellari S. Prion disease: diagnostic value of cerebrospinal fluid markers. Nature Reviews. Neurology. 9: 10-1. PMID 23208112 DOI: 10.1038/nrneurol.2012.253  0.96
2013 Gelpi E, Soler Insa JM, Parchi P, Saverioni D, Yagüe J, Nos C, Martínez-Saez E, Ribalta T, Ferrer I, Sanchez-Valle R. Atypical neuropathological sCJD-MM phenotype with abundant white matter Kuru-type plaques sparing the cerebellar cortex. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 33: 204-8. PMID 22862687 DOI: 10.1111/j.1440-1789.2012.01341.x  0.96
2012 Durrenberger PF, Fernando FS, Magliozzi R, Kashefi SN, Bonnert TP, Ferrer I, Seilhean D, Nait-Oumesmar B, Schmitt A, Gebicke-Haerter PJ, Falkai P, Grünblatt E, Palkovits M, Parchi P, Capellari S, et al. Selection of novel reference genes for use in the human central nervous system: a BrainNet Europe Study. Acta Neuropathologica. 124: 893-903. PMID 22864814 DOI: 10.1007/s00401-012-1027-z  0.96
2012 Parchi P, de Boni L, Saverioni D, Cohen ML, Ferrer I, Gambetti P, Gelpi E, Giaccone G, Hauw JJ, Höftberger R, Ironside JW, Jansen C, Kovacs GG, Rozemuller A, Seilhean D, et al. Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA. Acta Neuropathologica. 124: 517-29. PMID 22744790 DOI: 10.1007/s00401-012-1002-8  0.96
2012 Alafuzoff I, Gelpi E, Al-Sarraj S, Arzberger T, Attems J, Bodi I, Bogdanovic N, Budka H, Bugiani O, Englund E, Ferrer I, Gentleman S, Giaccone G, Graeber MB, Hortobagyi T, ... ... Parchi P, et al. The need to unify neuropathological assessments of vascular alterations in the ageing brain: multicentre survey by the BrainNet Europe consortium. Experimental Gerontology. 47: 825-33. PMID 22705312 DOI: 10.1016/j.exger.2012.06.001  0.96
2012 Jansen C, Parchi P, Capellari S, Ibrahim-Verbaas CA, Schuur M, Strammiello R, Corrado P, Bishop MT, van Gool WA, Verbeek MM, Baas F, van Saane W, Spliet WG, Jansen GH, van Duijn CM, et al. Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects. Plos One. 7: e36333. PMID 22558438 DOI: 10.1371/journal.pone.0036333  0.96
2012 Parchi P, Saverioni D. Molecular pathology, classification, and diagnosis of sporadic human prion disease variants. Folia Neuropathologica / Association of Polish Neuropathologists and Medical Research Centre, Polish Academy of Sciences. 50: 20-45. PMID 22505361  0.96
2012 Cerullo F, Del Nonno F, Baiocchini A, Parchi P, Cesari M, Gambassi G. Creutzfeldt-Jakob disease: an under-recognized cause of dementia. Journal of the American Geriatrics Society. 60: 156-7. PMID 22239296 DOI: 10.1111/j.1532-5415.2011.03756.x  0.96
2012 Popova SN, Tarvainen I, Capellari S, Parchi P, Hannikainen P, Pirinen E, Haapasalo H, Alafuzoff I. Divergent clinical and neuropathological phenotype in a Gerstmann-Sträussler-Scheinker P102L family. Acta Neurologica Scandinavica. 126: 315-23. PMID 22211828 DOI: 10.1111/j.1600-0404.2011.01628.x  0.96
2012 Rizzi R, Zucco R, Bernardi A, Ghidoni E, Marcello N, De Berti G, Ragazzi M, Gardini G, Parchi P. SUDEP after epileptic seizure in limbic encephalitis caused by acute myocardial ischemia: Autopsy results | Morte improvvisa per infarto miocardico dopo crisi epilettica in paziente con encefalite limbica: Risultati autoptici Bollettino - Lega Italiana Contro L'Epilessia. 18-23.  0.96
2011 Jansen C, Parchi P, Capellari S, Strammiello R, Dopper EG, van Swieten JC, Kamphorst W, Rozemuller AJ. A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient. Journal of Neuropathology and Experimental Neurology. 70: 698-702. PMID 21760536 DOI: 10.1097/NEN.0b013e3182270c54  0.96
2011 Giaccone G, Arzberger T, Alafuzoff I, Al-Sarraj S, Budka H, Duyckaerts C, Falkai P, Ferrer I, Ironside JW, Kovács GG, Meyronet D, Parchi P, Patsouris E, Revesz T, Riederer P, et al. New lexicon and criteria for the diagnosis of Alzheimer's disease. The Lancet. Neurology. 10: 298-9; author reply . PMID 21435593 DOI: 10.1016/S1474-4422(11)70055-2  0.96
2011 Parchi P, Strammiello R, Giese A, Kretzschmar H. Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future. Acta Neuropathologica. 121: 91-112. PMID 21107851 DOI: 10.1007/s00401-010-0779-6  0.96
2011 Capellari S, Strammiello R, Saverioni D, Kretzschmar H, Parchi P. Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis. Acta Neuropathologica. 121: 21-37. PMID 20978903 DOI: 10.1007/s00401-010-0760-4  0.96
2011 Jansen C, Parchi P, Jelles B, Gouw AA, Beunders G, van Spaendonk RM, van de Kamp JM, Lemstra AW, Capellari S, Rozemuller AJ. The first case of fatal familial insomnia (FFI) in the Netherlands: a patient from Egyptian descent with concurrent four repeat tau deposits. Neuropathology and Applied Neurobiology. 37: 549-53. PMID 20874730 DOI: 10.1111/j.1365-2990.2010.01126.x  0.96
2011 Jansen C, Voet W, Head MW, Parchi P, Yull H, Verrips A, Wesseling P, Meulstee J, Baas F, van Gool WA, Ironside JW, Rozemuller AJ. A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literature. Acta Neuropathologica. 121: 59-68. PMID 20198483 DOI: 10.1007/s00401-010-0656-3  0.96
2011 Parchi P, Capellari S, Gambetti P. Fatal Familial and Sporadic Insomnia Neurodegeneration: the Molecular Pathology of Dementia and Movement Disorders: Second Edition. 346-349. DOI: 10.1002/9781444341256.ch34  0.96
2011 Budka H, Head MW, Ironside JW, Gambetti P, Parchi P, Tagliavini F. Sporadic Creutzfeldt-Jakob Disease Neurodegeneration: the Molecular Pathology of Dementia and Movement Disorders: Second Edition. 322-335. DOI: 10.1002/9781444341256.ch32  0.96
2010 Parchi P, Cescatti M, Notari S, Schulz-Schaeffer WJ, Capellari S, Giese A, Zou WQ, Kretzschmar H, Ghetti B, Brown P. Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease. Brain : a Journal of Neurology. 133: 3030-42. PMID 20823086 DOI: 10.1093/brain/awq234  0.96
2010 Masullo C, Bizzarro A, Guglielmi V, Iannaccone E, Minicuci G, Vita MG, Capellari S, Parchi P, Servidei S. An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 31: 837-9. PMID 20730466 DOI: 10.1007/s10072-010-0388-0  0.96
2010 Zou WQ, Puoti G, Xiao X, Yuan J, Qing L, Cali I, Shimoji M, Langeveld JP, Castellani R, Notari S, Crain B, Schmidt RE, Geschwind M, Dearmond SJ, Cairns NJ, ... ... Parchi P, et al. Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein. Annals of Neurology. 68: 162-72. PMID 20695009 DOI: 10.1002/ana.22094  0.96
2010 Zou WQ, Langeveld J, Xiao X, Chen S, McGeer PL, Yuan J, Payne MC, Kang HE, McGeehan J, Sy MS, Greenspan NS, Kaplan D, Wang GX, Parchi P, Hoover E, et al. PrP conformational transitions alter species preference of a PrP-specific antibody. The Journal of Biological Chemistry. 285: 13874-84. PMID 20194495 DOI: 10.1074/jbc.M109.088831  0.96
2010 Notari S, Moleres FJ, Hunter SB, Belay ED, Schonberger LB, Cali I, Parchi P, Shieh WJ, Brown P, Zaki S, Zou WQ, Gambetti P. Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States. Plos One. 5: e8765. PMID 20098730 DOI: 10.1371/journal.pone.0008765  0.96
2010 Jansen C, Parchi P, Capellari S, Vermeij AJ, Corrado P, Baas F, Strammiello R, van Gool WA, van Swieten JC, Rozemuller AJ. Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP. Acta Neuropathologica. 119: 189-97. PMID 19911184 DOI: 10.1007/s00401-009-0609-x  0.96
2010 Kovacs GG, Sanchez-Juan P, Ströbel T, Schuur M, Poleggi A, Nocentini S, Giannattasio C, Belay G, Bishop M, Capellari S, Parchi P, Gelpi E, Gal A, Bakos A, Molnar MJ, et al. Cathepsin D (C224T) polymorphism in sporadic and genetic Creutzfeldt-Jakob disease. Alzheimer Disease and Associated Disorders. 24: 104-7. PMID 19571726 DOI: 10.1097/WAD.0b013e3181ad378c  0.96
2010 Zou WQ, Langeveld J, Xiao X, Chen S, McGeer PL, Yuan J, Payne MC, Kang HE, McGeehan J, Sy MS, Greenspan NS, Kaplan D, Wang GX, Parchi P, Hoover E, et al. Reply to Kascsak: Definition of the PrP 3F4 epitope revisited Journal of Biological Chemistry. 285: le6. DOI: 10.1074/jbc.N109.088831  0.96
2009 Jansen C, van Swieten JC, Capellari S, Strammiello R, Parchi P, Rozemuller AJ. Inherited Creutzfeldt-Jakob disease in a Dutch patient with a novel five octapeptide repeat insertion and unusual cerebellar morphology. Journal of Neurology, Neurosurgery, and Psychiatry. 80: 1386-9. PMID 19917818 DOI: 10.1136/jnnp.2008.169359  0.96
2009 Lodi R, Parchi P, Tonon C, Manners D, Capellari S, Strammiello R, Rinaldi R, Testa C, Malucelli E, Mostacci B, Rizzo G, Pierangeli G, Cortelli P, Montagna P, Barbiroli B. Magnetic resonance diagnostic markers in clinically sporadic prion disease: a combined brain magnetic resonance imaging and spectroscopy study. Brain : a Journal of Neurology. 132: 2669-79. PMID 19755520 DOI: 10.1093/brain/awp210  0.96
2009 Cali I, Castellani R, Alshekhlee A, Cohen Y, Blevins J, Yuan J, Langeveld JP, Parchi P, Safar JG, Zou WQ, Gambetti P. Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics. Brain : a Journal of Neurology. 132: 2643-58. PMID 19734292 DOI: 10.1093/brain/awp196  0.96
2009 Parchi P, Strammiello R, Notari S, Giese A, Langeveld JP, Ladogana A, Zerr I, Roncaroli F, Cras P, Ghetti B, Pocchiari M, Kretzschmar H, Capellari S. Incidence and spectrum of sporadic Creutzfeldt-Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification. Acta Neuropathologica. 118: 659-71. PMID 19718500 DOI: 10.1007/s00401-009-0585-1  0.96
2009 Mancuso M, Siciliano G, Capellari S, Orsucci D, Moretti P, Di Fede G, Suardi S, Strammiello R, Parchi P, Tagliavini F, Murri L. Creutzfeldt-Jakob disease with E200K PRNP mutation: a case report and revision of the literature. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 30: 417-20. PMID 19597763 DOI: 10.1007/s10072-009-0118-7  0.96
2009 Baldin E, Capellari S, Provini F, Corrado P, Liguori R, Parchi P, Montagna P, Cortelli P. A case of fatal familial insomnia in Africa. Journal of Neurology. 256: 1778-9. PMID 19526349 DOI: 10.1007/s00415-009-5205-4  0.96
2009 Manners DN, Parchi P, Tonon C, Capellari S, Strammiello R, Testa C, Tani G, Malucelli E, Spagnolo C, Cortelli P, Montagna P, Lodi R, Barbiroli B. Pathologic correlates of diffusion MRI changes in Creutzfeldt-Jakob disease. Neurology. 72: 1425-31. PMID 19380702 DOI: 10.1212/WNL.0b013e3181a18846  0.96
2009 Alafuzoff I, Ince PG, Arzberger T, Al-Sarraj S, Bell J, Bodi I, Bogdanovic N, Bugiani O, Ferrer I, Gelpi E, Gentleman S, Giaccone G, Ironside JW, Kavantzas N, King A, ... ... Parchi P, et al. Staging/typing of Lewy body related alpha-synuclein pathology: a study of the BrainNet Europe Consortium. Acta Neuropathologica. 117: 635-52. PMID 19330340 DOI: 10.1007/s00401-009-0523-2  0.96
2009 Alafuzoff I, Thal DR, Arzberger T, Bogdanovic N, Al-Sarraj S, Bodi I, Boluda S, Bugiani O, Duyckaerts C, Gelpi E, Gentleman S, Giaccone G, Graeber M, Hortobagyi T, Höftberger R, ... ... Parchi P, et al. Assessment of beta-amyloid deposits in human brain: a study of the BrainNet Europe Consortium. Acta Neuropathologica. 117: 309-20. PMID 19184666 DOI: 10.1007/s00401-009-0485-4  0.96
2009 La Morgia C, Parchi P, Capellari S, Lodi R, Tonon C, Rinaldi R, Mondini S, Cirignotta F. 'Agrypnia excitata' in a case of sporadic Creutzfeldt-Jakob disease VV2. Journal of Neurology, Neurosurgery, and Psychiatry. 80: 244-6. PMID 19151026 DOI: 10.1136/jnnp.2008.149344  0.96
2009 Ragno M, Scarcella MG, Cacchiò G, Capellari S, Di Marzio F, Parchi P, Trojano L. Striatal [123I] FP-CIT SPECT demonstrates dopaminergic deficit in a sporadic case of Creutzfeldt-Jakob disease. Acta Neurologica Scandinavica. 119: 131-4. PMID 18638039 DOI: 10.1111/j.1600-0404.2008.01075.x  0.96
2009 Parchi P, Notari S, Weber P, Schimmel H, Budka H, Ferrer I, Haik S, Hauw JJ, Head MW, Ironside JW, Limido L, Rodriguez A, Ströbel T, Tagliavini F, Kretzschmar HA. Inter-laboratory assessment of PrPSc typing in creutzfeldt-jakob disease: a Western blot study within the NeuroPrion Consortium. Brain Pathology (Zurich, Switzerland). 19: 384-91. PMID 18624793 DOI: 10.1111/j.1750-3639.2008.00187.x  0.96
2008 Kovacs GG, Alafuzoff I, Al-Sarraj S, Arzberger T, Bogdanovic N, Capellari S, Ferrer I, Gelpi E, Kövari V, Kretzschmar H, Nagy Z, Parchi P, Seilhean D, Soininen H, Troakes C, et al. Mixed brain pathologies in dementia: the BrainNet Europe consortium experience. Dementia and Geriatric Cognitive Disorders. 26: 343-50. PMID 18849605 DOI: 10.1159/000161560  0.96
2008 Rizzo G, Martinelli P, Manners D, Scaglione C, Tonon C, Cortelli P, Malucelli E, Capellari S, Testa C, Parchi P, Montagna P, Barbiroli B, Lodi R. Diffusion-weighted brain imaging study of patients with clinical diagnosis of corticobasal degeneration, progressive supranuclear palsy and Parkinson's disease. Brain : a Journal of Neurology. 131: 2690-700. PMID 18819991 DOI: 10.1093/brain/awn195  0.96
2008 Notari S, Strammiello R, Capellari S, Giese A, Cescatti M, Grassi J, Ghetti B, Langeveld JP, Zou WQ, Gambetti P, Kretzschmar HA, Parchi P. Characterization of truncated forms of abnormal prion protein in Creutzfeldt-Jakob disease. The Journal of Biological Chemistry. 283: 30557-65. PMID 18753138 DOI: 10.1074/jbc.M801877200  0.96
2008 Ferrer I, Martinez A, Boluda S, Parchi P, Barrachina M. Brain banks: benefits, limitations and cautions concerning the use of post-mortem brain tissue for molecular studies. Cell and Tissue Banking. 9: 181-94. PMID 18543077 DOI: 10.1007/s10561-008-9077-0  0.96
2008 Alafuzoff I, Arzberger T, Al-Sarraj S, Bodi I, Bogdanovic N, Braak H, Bugiani O, Del-Tredici K, Ferrer I, Gelpi E, Giaccone G, Graeber MB, Ince P, Kamphorst W, King A, ... ... Parchi P, et al. Staging of neurofibrillary pathology in Alzheimer's disease: a study of the BrainNet Europe Consortium. Brain Pathology (Zurich, Switzerland). 18: 484-96. PMID 18371174 DOI: 10.1111/j.1750-3639.2008.00147.x  0.96
2008 Bell JE, Alafuzoff I, Al-Sarraj S, Arzberger T, Bogdanovic N, Budka H, Dexter DT, Falkai P, Ferrer I, Gelpi E, Gentleman SM, Giaccone G, Huitinga I, Ironside JW, Klioueva N, ... ... Parchi P, et al. Management of a twenty-first century brain bank: experience in the BrainNet Europe consortium. Acta Neuropathologica. 115: 497-507. PMID 18365220 DOI: 10.1007/s00401-008-0360-8  0.96
2008 Alafuzoff I, Pikkarainen M, Arzberger T, Thal DR, Al-Sarraj S, Bell J, Bodi I, Budka H, Capetillo-Zarate E, Ferrer I, Gelpi E, Gentleman S, Giaccone G, Kavantzas N, King A, ... ... Parchi P, et al. Inter-laboratory comparison of neuropathological assessments of beta-amyloid protein: a study of the BrainNet Europe consortium. Acta Neuropathologica. 115: 533-46. PMID 18343933 DOI: 10.1007/s00401-008-0358-2  0.96
2008 Capellari S, Parchi P, Cortelli P, Avoni P, Casadei GP, Bini C, Baruzzi A, Lugaresi E, Pocchiari M, Gambetti P, Montagna P. Sporadic fatal insomnia in a fatal familial insomnia pedigree. Neurology. 70: 884-5. PMID 18332347 DOI: 10.1212/01.wnl.0000287140.94379.52  0.96
2008 Alafuzoff I, Parkkinen L, Al-Sarraj S, Arzberger T, Bell J, Bodi I, Bogdanovic N, Budka H, Ferrer I, Gelpi E, Gentleman S, Giaccone G, Kamphorst W, King A, Korkolopoulou P, ... ... Parchi P, et al. Assessment of alpha-synuclein pathology: a study of the BrainNet Europe Consortium. Journal of Neuropathology and Experimental Neurology. 67: 125-43. PMID 18219257 DOI: 10.1097/nen.0b013e3181633526  0.96
2008 Cortelli P, Perani D, Montagna P, Gallassi R, Tinuper P, Provini F, Avoni P, Ferrillo F, Anchisi D, Moresco RM, Fazio F, Parchi P, Baruzzi A, Lugaresi E, Gambetti P. Pre-symptomatic diagnosis in fatal familial insomnia: Serial neurophysiological and 18FDG-PET studies (Brain (March 2006) 129: part 3 (668-675) doi: 10.1093/brain/awl003) Brain. 131: 1161. DOI: 10.1093/brain/awn067  0.96
2007 Notari S, Capellari S, Langeveld J, Giese A, Strammiello R, Gambetti P, Kretzschmar HA, Parchi P. A refined method for molecular typing reveals that co-occurrence of PrP(Sc) types in Creutzfeldt-Jakob disease is not the rule. Laboratory Investigation; a Journal of Technical Methods and Pathology. 87: 1103-12. PMID 17893675 DOI: 10.1038/labinvest.3700676  0.96
2007 Ferrer I, Armstrong J, Capellari S, Parchi P, Arzberger T, Bell J, Budka H, Ströbel T, Giaccone G, Rossi G, Bogdanovic N, Fakai P, Schmitt A, Riederers P, Al-Sarraj S, et al. Effects of formalin fixation, paraffin embedding, and time of storage on DNA preservation in brain tissue: a BrainNet Europe study. Brain Pathology (Zurich, Switzerland). 17: 297-303. PMID 17465988 DOI: 10.1111/j.1750-3639.2007.00073.x  0.96
2007 Magherini A, Pentore R, Galassi G, Stucchi CM, Capellari S, Parchi P. MV2 subtype of sporadic Creutzfeldt-Jakob disease presenting as corticobasal syndrome. Movement Disorders : Official Journal of the Movement Disorder Society. 22: 898-9. PMID 17393534 DOI: 10.1002/mds.21426  0.96
2007 Ferrer I, Santpere G, Arzberger T, Bell J, Blanco R, Boluda S, Budka H, Carmona M, Giaccone G, Krebs B, Limido L, Parchi P, Puig B, Strammiello R, Ströbel T, et al. Brain protein preservation largely depends on the postmortem storage temperature: implications for study of proteins in human neurologic diseases and management of brain banks: a BrainNet Europe Study. Journal of Neuropathology and Experimental Neurology. 66: 35-46. PMID 17204935 DOI: 10.1097/nen.0b013e31802c3e7d  0.96
2007 Schmitt A, Bauer M, Heinsen H, Feiden W, Falkai P, Alafuzoff I, Arzberger T, Al-Sarraj S, Bell JE, Bogdanovic N, Brück W, Budka H, Ferrer I, Giaccone G, ... ... Parchi P, et al. How a neuropsychiatric brain bank should be run: a consensus paper of Brainnet Europe II. Journal of Neural Transmission (Vienna, Austria : 1996). 114: 527-37. PMID 17165101 DOI: 10.1007/s00702-006-0601-8  0.96
2006 Cali I, Castellani R, Yuan J, Al-Shekhlee A, Cohen ML, Xiao X, Moleres FJ, Parchi P, Zou WQ, Gambetti P. Classification of sporadic Creutzfeldt-Jakob disease revisited. Brain : a Journal of Neurology. 129: 2266-77. PMID 16923954 DOI: 10.1093/brain/awl224  0.96
2006 Alafuzoff I, Pikkarainen M, Al-Sarraj S, Arzberger T, Bell J, Bodi I, Bogdanovic N, Budka H, Bugiani O, Ferrer I, Gelpi E, Giaccone G, Graeber MB, Hauw JJ, Kamphorst W, ... ... Parchi P, et al. Interlaboratory comparison of assessments of Alzheimer disease-related lesions: a study of the BrainNet Europe Consortium. Journal of Neuropathology and Experimental Neurology. 65: 740-57. PMID 16896308 DOI: 10.1097/01.jnen.0000229986.17548.27  0.96
2006 Cortelli P, Perani D, Montagna P, Gallassi R, Tinuper P, Provini F, Federica P, Avoni P, Ferrillo F, Anchisi D, Moresco RM, Fazio F, Parchi P, Baruzzi A, Lugaresi E, et al. Pre-symptomatic diagnosis in fatal familial insomnia: serial neurophysiological and 18FDG-PET studies. Brain : a Journal of Neurology. 129: 668-75. PMID 16399807 DOI: 10.1093/brain/awl003  0.96
2006 Prusiner SB. History of prion research Prions in Humans and Animals. 44-57. DOI: 10.1515/9783110200171  0.36
2005 Capellari S, Cardone F, Notari S, Schininà ME, Maras B, Sità D, Baruzzi A, Pocchiari M, Parchi P. Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene. Neurology. 64: 905-7. PMID 15753435 DOI: 10.1212/01.WNL.0000152837.82388.DE  0.96
2004 Chrétien F, Le Pavec G, Vallat-Decouvelaere AV, Delisle MB, Uro-Coste E, Ironside JW, Gambetti P, Parchi P, Créminon C, Dormont D, Mikol J, Gray F, Gras G. Expression of excitatory amino acid transporter-1 (EAAT-1) in brain macrophages and microglia of patients with prion diseases. Journal of Neuropathology and Experimental Neurology. 63: 1058-71. PMID 15535133  0.96
2004 Castellani RJ, Colucci M, Xie Z, Zou W, Li C, Parchi P, Capellari S, Pastore M, Rahbar MH, Chen SG, Gambetti P. Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease. Neurology. 63: 436-42. PMID 15304573  0.96
2004 Notari S, Capellari S, Giese A, Westner I, Baruzzi A, Ghetti B, Gambetti P, Kretzschmar HA, Parchi P. Effects of different experimental conditions on the PrPSc core generated by protease digestion: implications for strain typing and molecular classification of CJD. The Journal of Biological Chemistry. 279: 16797-804. PMID 14754888 DOI: 10.1074/jbc.M313220200  0.96
2003 Gambetti P, Kong Q, Zou W, Parchi P, Chen SG. Sporadic and familial CJD: classification and characterisation. British Medical Bulletin. 66: 213-39. PMID 14522861 DOI: 10.1093/bmb/66.1.213  0.96
2003 Zou WQ, Capellari S, Parchi P, Sy MS, Gambetti P, Chen SG. Identification of novel proteinase K-resistant C-terminal fragments of PrP in Creutzfeldt-Jakob disease. The Journal of Biological Chemistry. 278: 40429-36. PMID 12917418 DOI: 10.1074/jbc.M308550200  0.96
2003 Gambetti P, Parchi P, Chen SG. Hereditary Creutzfeldt-Jakob disease and fatal familial insomnia. Clinics in Laboratory Medicine. 23: 43-64. PMID 12733424 DOI: 10.1016/S0272-2712(02)00065-3  0.96
2003 Korth C, Kaneko K, Groth D, Heye N, Telling G, Mastrianni J, Parchi P, Gambetti P, Will R, Ironside J, Heinrich C, Tremblay P, DeArmond SJ, Prusiner SB. Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene. Proceedings of the National Academy of Sciences of the United States of America. 100: 4784-9. PMID 12684540 DOI: 10.1073/pnas.2627989100  0.96
2003 Schininá ME, Maras B, Cardone F, Mancone C, Principe S, Di Bari MA, Parchi P, Pocchiari M. Prion protein allotype profiling by mass spectrometry Pure and Applied Chemistry. 75: 317-323.  0.96
2002 Capellari S, Parchi P, Wolff BD, Campbell J, Atkinson R, Posey DM, Petersen RB, Gambetti P. Creutzfeldt-Jakob disease associated with a deletion of two repeats in the prion protein gene. Neurology. 59: 1628-30. PMID 12451210  0.96
2002 Beaudry P, Parchi P, Peoc'h K, Desbordes P, Dartigues JF, Vital A, Vital C, Capellari S, Gambetti P, Delasnerie-Lauprêtre N, Mary JY, Laplanche JL. A French cluster of Creutzfeldt-Jakob disease: a molecular analysis. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 9: 457-62. PMID 12220376 DOI: 10.1046/j.1468-1331.2002.00456.x  0.96
2001 Gambetti P, Parchi P, Capellari S, Russo C, Tabaton M, Teller JK, Chen SG. Mechanisms of phenotypic heterogeneity in prion, Alzheimer and other conformational diseases. Journal of Alzheimer's Disease : Jad. 3: 87-95. PMID 12214077  0.96
2001 Belay ED, Gambetti P, Schonberger LB, Parchi P, Lyon DR, Capellari S, McQuiston JH, Bradley K, Dowdle G, Crutcher JM, Nichols CR. Creutzfeldt-Jakob disease in unusually young patients who consumed venison. Archives of Neurology. 58: 1673-8. PMID 11594928  0.96
2001 Hannah EL, Belay ED, Gambetti P, Krause G, Parchi P, Capellari S, Hoffman RE, Schonberger LB. Creutzfeldt-Jakob disease after receipt of a previously unimplicated brand of dura mater graft. Neurology. 56: 1080-3. PMID 11320182  0.96
2001 Chen SG, Zou W, Parchi P, Gambetti P. PrPSc typing by N-terminal sequencing and mass spectrometry Archives of Virology, Supplement. 209-216.  0.96
2000 Chen SG, Zou W, Parchi P, Gambetti P. PrP(Sc) typing by N-terminal sequencing and mass spectrometry. Archives of Virology. Supplementum. 209-16. PMID 11214924  0.96
2000 Parchi P, Zou W, Wang W, Brown P, Capellari S, Ghetti B, Kopp N, Schulz-Schaeffer WJ, Kretzschmar HA, Head MW, Ironside JW, Gambetti P, Chen SG. Genetic influence on the structural variations of the abnormal prion protein. Proceedings of the National Academy of Sciences of the United States of America. 97: 10168-72. PMID 10963679 DOI: 10.1073/pnas.97.18.10168  0.96
2000 Capellari S, Parchi P, Russo CM, Sanford J, Sy MS, Gambetti P, Petersen RB. Effect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brain. The American Journal of Pathology. 157: 613-22. PMID 10934164 DOI: 10.1016/S0002-9440(10)64572-5  0.96
2000 Parchi P, Capellari S, Gambetti P. Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia. Microscopy Research and Technique. 50: 16-25. PMID 10871544 DOI: 10.1002/1097-0029(20000701)50:1<16::AID-JEMT4>3.0.CO;2-Y  0.96
2000 Chen SG, Parchi P, Gambetti P. 38. Prion diseases including bovine spongiform encephalopathy (mad cow disease) Facts, Research and Intervention in Geriatrics. 2000: 491-502.  0.96
1999 Worrall BB, Herman ST, Capellari S, Lynch T, Chin S, Gambetti P, Parchi P. Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease. Journal of Neurology, Neurosurgery, and Psychiatry. 67: 671-4. PMID 10519879 DOI: 10.1136/jnnp.67.5.671  0.96
1999 Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, Zerr I, Budka H, Kopp N, Piccardo P, Poser S, Rojiani A, Streichemberger N, Julien J, Vital C, et al. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Annals of Neurology. 46: 224-33. PMID 10443888 DOI: 10.1002/1531-8249(199908)46:2<224::AID-ANA12>3.0.CO;2-W  0.96
1999 Parchi P, Capellari S, Chin S, Schwarz HB, Schecter NP, Butts JD, Hudkins P, Burns DK, Powers JM, Gambetti P. A subtype of sporadic prion disease mimicking fatal familial insomnia. Neurology. 52: 1757-63. PMID 10371520  0.96
1999 Hainfellner JA, Parchi P, Kitamoto T, Jarius C, Gambetti P, Budka H. A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein. Annals of Neurology. 45: 812-6. PMID 10360778 DOI: 10.1002/1531-8249(199906)45:6<812::AID-ANA20>3.0.CO;2-2  0.96
1999 Gambetti P, Parchi P. Insomnia in prion diseases: sporadic and familial. The New England Journal of Medicine. 340: 1675-7. PMID 10341282 DOI: 10.1056/NEJM199905273402111  0.96
1999 Bahn MM, Parchi P. Abnormal diffusion-weighted magnetic resonance images in Creutzfeldt-Jakob disease. Archives of Neurology. 56: 577-83. PMID 10328253 DOI: 10.1001/archneur.56.5.577  0.96
1999 Goedert M, Spillantini MG, Crowther RA, Chen SG, Parchi P, Tabaton M, Lanska DJ, Markesbery WR, Wilhelmsen KC, Dickson DW, Petersen RB, Gambetti P. Tau gene mutation in familial progressive subcortical gliosis. Nature Medicine. 5: 454-7. PMID 10202939 DOI: 10.1038/7454  0.96
1999 Arnold SE, Trojanowski JQ, Parchi P. Protease resistant prion proteins are not present in sporadic "poor outcome" schizophrenia. Journal of Neurology, Neurosurgery, and Psychiatry. 66: 90-2. PMID 9886461  0.96
1998 Padovani A, D'Alessandro M, Parchi P, Cortelli P, Anzola GP, Montagna P, Vignolo LA, Petraroli R, Pocchiari M, Lugaresi E, Gambetti P. Fatal familial insomnia in a new Italian kindred. Neurology. 51: 1491-4. PMID 9818894  0.96
1998 Ghorayeb I, Series C, Parchi P, Sawan B, Guez S, Laplanche JL, Capellari S, Gambetti P, Vital C. Creutzfeldt-Jakob disease with long duration and panencephalopathic lesions: molecular analysis of one case. Neurology. 51: 271-4. PMID 9674819  0.96
1998 Parchi P, Petersen RB, Chen SG, Autilio-Gambetti L, Capellari S, Monari L, Cortelli P, Montagna P, Lugaresi E, Gambetti P. Molecular pathology of fatal familial insomnia. Brain Pathology (Zurich, Switzerland). 8: 539-48. PMID 9669705  0.96
1998 Dorandeu A, Wingertsmann L, Chrétien F, Delisle MB, Vital C, Parchi P, Montagna P, Lugaresi E, Ironside JW, Budka H, Gambetti P, Gray F. Neuronal apoptosis in fatal familial insomnia. Brain Pathology (Zurich, Switzerland). 8: 531-7. PMID 9669704  0.96
1998 Parchi P, Chen SG, Brown P, Zou W, Capellari S, Budka H, Hainfellner J, Reyes PF, Golden GT, Hauw JJ, Gajdusek DC, Gambetti P. Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease. Proceedings of the National Academy of Sciences of the United States of America. 95: 8322-7. PMID 9653185 DOI: 10.1073/pnas.95.14.8322  0.96
1998 Vital C, Gray F, Vital A, Parchi P, Capellari S, Petersen RB, Ferrer X, Jarnier D, Julien J, Gambetti P. Prion encephalopathy with insertion of octapeptide repeats: the number of repeats determines the type of cerebellar deposits. Neuropathology and Applied Neurobiology. 24: 125-30. PMID 9634208 DOI: 10.1046/j.1365-2990.1998.00098.x  0.96
1997 Pierangeli G, Parchi P, Barletta G, Chiogna M, Lugaresi E, Cortelli P. Power spectral analysis of heart rate and diastolic blood pressure variability in migraine with and without aura. Cephalalgia : An International Journal of Headache. 17: 756-60; discussion 7. PMID 9399005 DOI: 10.1046/j.1468-2982.1997.1707756.x  0.96
1997 Chen SG, Parchi P, Brown P, Capellari S, Zou W, Cochran EJ, Vnencak-Jones CL, Julien J, Vital C, Mikol J, Lugaresi E, Autilio-Gambetti L, Gambetti P. Allelic origin of the abnormal prion protein isoform in familial prion diseases. Nature Medicine. 3: 1009-15. PMID 9288728 DOI: 10.1038/nm0997-1009  0.96
1997 Capellari S, Vital C, Parchi P, Petersen RB, Ferrer X, Jarnier D, Pegoraro E, Gambetti P, Julien J. Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family. Neurology. 49: 133-41. PMID 9222181  0.96
1997 Cortelli P, Perani D, Parchi P, Grassi F, Montagna P, De Martin M, Castellani R, Tinuper P, Gambetti P, Lugaresi E, Fazio F. Cerebral metabolism in fatal familial insomnia: relation to duration, neuropathology, and distribution of protease-resistant prion protein. Neurology. 49: 126-33. PMID 9222180  0.96
1997 Castellani RJ, Parchi P, Madoff L, Gambetti P, McKeever P. Biopsy diagnosis of Creutzfeldt-Jakob disease by western blot: a case report. Human Pathology. 28: 623-6. PMID 9158712 DOI: 10.1016/S0046-8177(97)90086-1  0.96
1997 Parchi P, Capellari S, Chen SG, Petersen RB, Gambetti P, Kopp N, Brown P, Kitamoto T, Tateishi J, Giese A, Kretzschmar H. Typing prion isoforms. Nature. 386: 232-4. PMID 9069279 DOI: 10.1038/386232a0  0.96
1996 Telling GC, Parchi P, DeArmond SJ, Cortelli P, Montagna P, Gabizon R, Mastrianni J, Lugaresi E, Gambetti P, Prusiner SB. Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity. Science (New York, N.Y.). 274: 2079-82. PMID 8953038 DOI: 10.1126/science.274.5295.2079  0.96
1996 Parchi P, Castellani R, Capellari S, Ghetti B, Young K, Chen SG, Farlow M, Dickson DW, Sima AA, Trojanowski JQ, Petersen RB, Gambetti P. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease. Annals of Neurology. 39: 767-78. PMID 8651649 DOI: 10.1002/ana.410390613  0.96
1996 Sima AA, Defendini R, Keohane C, D'Amato C, Foster NL, Parchi P, Gambetti P, Lynch T, Wilhelmsen KC. The neuropathology of chromosome 17-linked dementia. Annals of Neurology. 39: 734-43. PMID 8651645 DOI: 10.1002/ana.410390609  0.96
1996 Castellani R, Parchi P, Stahl J, Capellari S, Cohen M, Gambetti P. Early pathologic and biochemical changes in Creutzfeldt-Jakob disease: study of brain biopsies. Neurology. 46: 1690-3. PMID 8649571 DOI: 10.1212/WNL.46.6.1690  0.96
1996 Petersen RB, Parchi P, Richardson SL, Urig CB, Gambetti P. Effect of the D178N mutation and the codon 129 polymorphism on the metabolism of the prion protein. The Journal of Biological Chemistry. 271: 12661-8. PMID 8647879 DOI: 10.1074/jbc.271.21.12661  0.96
1996 Parchi P, Petersen RB, Gambetti P. New topics in familial prion diseases Seminars in Virology. 7: 181-187. DOI: 10.1006/smvy.1996.0023  0.96
1995 Gambetti P, Parchi P, Petersen RB, Chen SG, Lugaresi E. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features. Brain Pathology (Zurich, Switzerland). 5: 43-51. PMID 7767490  0.96
1995 Créange A, Gray F, Cesaro P, Adle-Biassette H, Duvoux C, Cherqui D, Bell J, Parchi P, Gambetti P, Degos JD. Creutzfeldt-Jakob disease after liver transplantation. Annals of Neurology. 38: 269-72. PMID 7654078 DOI: 10.1002/ana.410380223  0.96
1995 Chen SG, Teplow DB, Parchi P, Teller JK, Gambetti P, Autilio-Gambetti L. Truncated forms of the human prion protein in normal brain and in prion diseases. The Journal of Biological Chemistry. 270: 19173-80. PMID 7642585 DOI: 10.1074/jbc.270.32.19173  0.96
1995 Parchi P, Castellani R, Cortelli P, Montagna P, Chen SG, Petersen RB, Manetto V, Vnencak-Jones CL, McLean MJ, Sheller JR. Regional distribution of protease-resistant prion protein in fatal familial insomnia. Annals of Neurology. 38: 21-9. PMID 7611720 DOI: 10.1002/ana.410380107  0.96
1995 Parchi P, Gambetti P. Human prion diseases. Current Opinion in Neurology. 8: 286-93. PMID 7582044  0.96
1994 Montagna P, Cortelli P, Monari L, Pierangeli G, Parchi P, Lodi R, Iotti S, Frassineti C, Zaniol P, Lugaresi E. 31P-magnetic resonance spectroscopy in migraine without aura. Neurology. 44: 666-9. PMID 8164822  0.96
1994 Cortelli P, Parchi P, Sforza E, Contin M, Pierangeli G, Barletta G, Lugaresi E. Cardiovascular autonomic dysfunction in normotensive awake subjects with obstructive sleep apnoea syndrome. Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society. 4: 57-62. PMID 8054838 DOI: 10.1007/BF01828839  0.96
1994 Monari L, Chen SG, Brown P, Parchi P, Petersen RB, Mikol J, Gray F, Cortelli P, Montagna P, Ghetti B. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism. Proceedings of the National Academy of Sciences of the United States of America. 91: 2839-42. PMID 7908444  0.96
1994 Sforza E, Parchi P, Contin M, Cortelli P, Lugaresi E. Do autonomic cardiovascular reflexes predict the nocturnal rise in blood pressure in obstructive sleep apnea syndrome? Blood Pressure. 3: 295-302. PMID 7866593 DOI: 10.3109/08037059409102277  0.96
1993 Parchi P, Pierangeli G, Verlicchi A, Cortelli P. Non-invasive continuous cardiovascular monitoring in the vasodepressor form of carotid sinus hypersensitivity--confirmation of its value. Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society. 3: 81-2. PMID 8477183  0.36
1992 Pierangeli G, Lugaresi A, Contin M, Martinelli P, Montagna P, Parchi P, Verlicchi A, Cortelli P. Autonomic nervous system function in myotonic dystrophy. Italian Journal of Neurological Sciences. 13: 589-92. PMID 1428793 DOI: 10.1007/BF02233402  0.96
1992 Cortelli P, Parchi P, Contin M, Sforza E, Lugaresi A, Pasquali R, Lugaresi E. Isolated failure of noradrenergic transmission in a case with orthostatic hypotension and hyperactivity of gastro-colic reflex. Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society. 2: 177-82. PMID 1323364 DOI: 10.1007/BF01818959  0.96
1991 Cortelli P, Parchi P, Contin M, Pierangeli G, Avoni P, Tinuper P, Montagna P, Baruzzi A, Gambetti PL, Lugaresi E. Cardiovascular dysautonomia in fatal familial insomnia. Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society. 1: 15-21. PMID 1821660 DOI: 10.1007/BF01826053  0.96
1991 Avoni P, Cortelli P, Montagna P, Tinuper P, Sforza E, Contin M, Parchi P, Pierangeli G, Maltoni P, Pavani A. Circadian hormonal rhythms in two new cases of fatal familial insomnia. Acta Neurologica. 13: 574-6. PMID 1805556  0.96
1991 Cortelli P, Pierangeli G, Parchi P, Contin M, Baruzzi A, Lugaresi E. Autonomic nervous system function in migraine without aura. Headache. 31: 457-62. PMID 1774161  0.96
1990 Calzá L, Giardino L, Zanni M, Velardo A, Parchi P, Marrama P. Daily changes of neuropeptide Y-like immunoreactivity in the suprachiasmatic nucleus of the rat. Regulatory Peptides. 27: 127-37. PMID 2408111 DOI: 10.1016/0167-0115(90)90211-E  0.96
1989 Giardino L, Calzà L, Zanni M, Parchi P, Battistini N, Marrama P. Iodinated-NPY binding sites: autoradiographic study in the rat brain. Neuropeptides. 13: 23-8. PMID 2537936 DOI: 10.1016/0143-4179(89)90017-6  0.96
1987 Giardino L, Calzà L, Galetti R, Parchi P, Galetti G. [Autoradiographic mapping of neurotransmitters and drug receptors in the vestibular nuclei complex of the rat]. Acta Otorhinolaryngologica Italica : Organo Ufficiale Della Società Italiana Di Otorinolaringologia E Chirurgia Cervico-Facciale. 7: 581-7. PMID 2842998  0.96
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