Sabina Capellari - Publications

Affiliations: 
Università di Bologna, Bologna, Italy 

151 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
2021 Sarapura-Castro E, Cosentino C, Landman J, Landman A, Torres L, Nuñez Y, Capellari S, Parchi P, Cornejo-Olivas M. Early sensory disturbances and seizures are common manifestations of familial Creutzfeldt-Jakob disease due to E200K PRNP mutation: Case report from two Peruvian families. Clinical Neurology and Neurosurgery. 202: 106490. PMID 33454496 DOI: 10.1016/j.clineuro.2021.106490  1
2020 Pirazzini C, Azevedo T, Baldelli L, Bartoletti-Stella A, Calandra-Buonaura G, Molin AD, Dimitri GM, Doykov I, Gómez-Garre P, Hägg S, Hällqvist J, Halsband C, Heywood W, Jesús S, Jylhävä J, ... ... Capellari S, et al. A Geroscience approach for Parkinson's Disease: conceptual framework and design of PROPAG-AGEING project. Mechanisms of Ageing and Development. 111426. PMID 33385396 DOI: 10.1016/j.mad.2020.111426  0.8
2020 Ratti S, Rusciano I, Mongiorgi S, Owusu Obeng E, Cappellini A, Teti G, Falconi M, Talozzi L, Capellari S, Bartoletti-Stella A, Guaraldi P, Cortelli P, Suh PG, Cocco L, Manzoli L, et al. Cell signaling pathways in autosomal-dominant leukodystrophy (ADLD): the intriguing role of the astrocytes. Cellular and Molecular Life Sciences : Cmls. PMID 33034697 DOI: 10.1007/s00018-020-03661-1  0.8
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, ... ... Capellari S, 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  1
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  1
2020 Romagnoli M, Stanzani Maserati M, De Matteis M, Capellari S, Carbonelli M, Amore G, Cantalupo G, Zenesini C, Liguori R, Sadun AA, Carelli V, Park JC, La Morgia C. Chromatic Pupillometry Findings in Alzheimer's Disease. Frontiers in Neuroscience. 14: 780. PMID 32848556 DOI: 10.3389/fnins.2020.00780  0.8
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  1
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, ... Capellari S, 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  1
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, 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  1
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  1
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  1
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  1
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  0.76
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2019 Stanzani Maserati M, Mitolo M, Medici F, D'Onofrio R, Oppi F, Poda R, De Matteis M, Tonon C, Lodi R, Liguori R, Capellari S. Color Choice Preference in Cognitively Impaired Patients: A Look Inside Alzheimer's Disease Through the Use of Lüscher Color Diagnostic. Frontiers in Psychology. 10: 1951. PMID 31507498 DOI: 10.3389/fpsyg.2019.01951  0.64
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  1
2019 Giorgio E, Lorenzati M, Rivetti di Val Cervo P, Brussino A, Cernigoj M, Della Sala E, Bartoletti Stella A, Ferrero M, Caiazzo M, Capellari S, Cortelli P, Conti L, Cattaneo E, Buffo A, Brusco A. Allele-specific silencing as treatment for gene duplication disorders: proof-of-principle in autosomal dominant leukodystrophy. Brain : a Journal of Neurology. PMID 31143934 DOI: 10.1093/brain/awz139  0.76
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  1
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  1
2019 Fileccia E, Di Stasi V, Poda R, Rizzo G, Stanzani-Maserati M, Oppi F, Avoni P, Capellari S, Liguori R. Effects on cognition of 20-day anodal transcranial direct current stimulation over the left dorsolateral prefrontal cortex in patients affected by mild cognitive impairment: a case-control study. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. PMID 31062189 DOI: 10.1007/s10072-019-03903-6  0.64
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  1
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  1
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  1
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  1
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  1
2018 Sambati L, Baldelli L, Calandra Buonaura G, Capellari S, Giannini G, Scaglione CLM, Armaroli M, Zoni E, Cortelli P, Martinelli P. Observing movement disorders: best practice proposal in the use of video recording in clinical practice. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. PMID 30448965 DOI: 10.1007/s10072-018-3639-0  0.76
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  1
2018 Contin M, Lopane G, Mohamed S, Calandra-Buonaura G, Capellari S, De Massis P, Nassetti S, Perrone A, Riva R, Sambati L, Scaglione C, Cortelli P. Clinical pharmacokinetics of pramipexole, ropinirole and rotigotine in patients with Parkinson's disease. Parkinsonism & Related Disorders. PMID 30446407 DOI: 10.1016/j.parkreldis.2018.11.007  0.76
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  1
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  1
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, et al. Sporadic Fatal Insomnia in Europe: Phenotypic features and diagnostic challenges. Annals of Neurology. PMID 30048013 DOI: 10.1002/ana.25300  1
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  1
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  1
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  1
2018 Gramegna LL, Evangelisti S, Testa C, Baiardi S, Mitolo M, Capellari S, Stracciari A, Poda R, Di Stasi V, Cretella L, Lodi R, Tonon C, Liguori R. Cognitive Rehabilitation and Transcranial Direct Current Stimulation in a Patient with Posterior Cortical Atrophy: An fMRI Study. The American Journal of Case Reports. 19: 729-733. PMID 29925828 DOI: 10.12659/AJCR.909167  0.8
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, ... ... Capellari S, 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  1
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  1
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  1
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  1
2018 Stanzani Maserati M, D'Onofrio R, Matacena C, Sambati L, Oppi F, Poda R, De Matteis M, Naldi I, Liguori R, Capellari S. Human figure drawing distinguishes Alzheimer's patients: a cognitive screening test study. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. PMID 29455399 DOI: 10.1007/s10072-018-3288-3  0.64
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2017 Donadio V, Incensi A, Rizzo G, Capellari S, Pantieri R, Stanzani Maserati M, Devigili G, Eleopra R, Defazio G, Montini F, Baruzzi A, Liguori R. A new potential biomarker for dementia with Lewy bodies: Skin nerve α-synuclein deposits. Neurology. PMID 28667178 DOI: 10.1212/WNL.0000000000004146  0.48
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  1
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  1
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  1
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  1
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  1
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  1
2016 Terlizzi R, Calandra-Buonaura G, Zanigni S, Barletta G, Capellari S, Guaraldi P, Donadio V, Cason E, Contin M, Poda R, Tonon C, Sambati L, Gallassi R, Liguori R, Lodi R, et al. A longitudinal study of a family with adult-onset autosomal dominant leukodystrophy: Clinical, autonomic and neuropsychological findings. Autonomic Neuroscience : Basic & Clinical. PMID 26896090 DOI: 10.1016/j.autneu.2016.02.005  0.76
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, ... ... Capellari S, et al. Quantifying prion disease penetrance using large population control cohorts. Science Translational Medicine. 8: 322ra9. PMID 26791950 DOI: 10.1126/scitranslmed.aad5169  0.92
2015 Garagnani P, Terlizzi R, Cevoli S, Capellari S, Pierangeli G, Pirazzini C, Bacalini MG, Franceschi C, Cortelli P. Genomics and epigenomics. The Journal of Headache and Pain. 16: A7. PMID 28132381 DOI: 10.1186/1129-2377-16-S1-A7  0.76
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  1
2015 Rizzo G, Licchetta L, Scaglione C, Buttiglione M, Capellari S, Martinelli P, Martino D. Behçet disease presenting with movement disorders and anti basal ganglia antibodies. Autoimmunity Reviews. PMID 26640160 DOI: 10.1016/j.autrev.2015.11.011  0.92
2015 Calandra-Buonaura G, Doria A, Lopane G, Guaraldi P, Capellari S, Martinelli P, Cortelli P, Contin M. Pharmacodynamics of a low subacute levodopa dose helps distinguish between multiple system atrophy with predominant Parkinsonism and Parkinson's disease. Journal of Neurology. PMID 26566913 DOI: 10.1007/s00415-015-7961-7  0.92
2015 Bartoletti-Stella A, Chiaro G, Calandra-Buonaura G, Contin M, Scaglione C, Barletta G, Cecere A, Garagnani P, Tieri P, Ferrarini A, Piras S, Franceschi C, Delledonne M, Cortelli P, Capellari S. A patient with PMP22-related hereditary neuropathy and DBH-gene-related dysautonomia. Journal of Neurology. 262: 2373-81. PMID 26410747 DOI: 10.1007/s00415-015-7896-z  0.92
2015 Zanigni S, Terlizzi R, Tonon C, Testa C, Manners DN, Capellari S, Gallassi R, Poda R, Gramegna LL, Calandra-Buonaura G, Sambati L, Cortelli P, Lodi R. Brain magnetic resonance metabolic and microstructural changes in adult-onset autosomal dominant leukodystrophy. Brain Research Bulletin. 117: 24-31. PMID 26189928 DOI: 10.1016/j.brainresbull.2015.07.002  0.92
2015 Giannoccaro MP, Donadio V, Incensi A, Pizza F, Cason E, Di Stasi V, Martinelli P, Scaglione C, Capellari S, Treglia G, Liguori R. Skin biopsy and I-123 MIBG scintigraphy findings in idiopathic Parkinson's disease and parkinsonism: A comparative study. Movement Disorders : Official Journal of the Movement Disorder Society. 30: 986-9. PMID 25778097 DOI: 10.1002/mds.26189  0.92
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  0.92
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  0.92
2014 Antelmi E, Rizzo G, Fabbri M, Capellari S, Scaglione C, Martinelli P. Arylsulphatase A activity in familial parkinsonism: a pathogenetic role? Journal of Neurology. 261: 1803-9. PMID 24989669 DOI: 10.1007/s00415-014-7425-5  0.92
2014 Ferrera D, Canale C, Marotta R, Mazzaro N, Gritti M, Mazzanti M, Capellari S, Cortelli P, Gasparini L. Lamin B1 overexpression increases nuclear rigidity in autosomal dominant leukodystrophy fibroblasts. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 28: 3906-18. PMID 24858279 DOI: 10.1096/fj.13-247635  0.92
2014 Donadio V, Incensi A, Leta V, Giannoccaro MP, Scaglione C, Martinelli P, Capellari S, Avoni P, Baruzzi A, Liguori R. Skin nerve α-synuclein deposits: a biomarker for idiopathic Parkinson disease. Neurology. 82: 1362-9. PMID 24634456 DOI: 10.1212/WNL.0000000000000316  0.92
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  0.92
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  0.92
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  0.92
2013 Giorgio E, Rolyan H, Kropp L, Chakka AB, Yatsenko S, Di Gregorio E, Lacerenza D, Vaula G, Talarico F, Mandich P, Toro C, Pierre EE, Labauge P, Capellari S, Cortelli P, et al. Analysis of LMNB1 duplications in autosomal dominant leukodystrophy provides insights into duplication mechanisms and allele-specific expression. Human Mutation. 34: 1160-71. PMID 23649844 DOI: 10.1002/humu.22348  0.92
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  0.92
2013 Martinelli P, Rizzo G, Scaglione C, Capellari S. Neurosyphilis orofacial dyskinesia: the candy sign. Movement Disorders : Official Journal of the Movement Disorder Society. 28: 246-7. PMID 23166011 DOI: 10.1002/mds.25281  0.92
2013 Sambati L, Agati R, Bacci A, Bianchi S, Capellari S. Vanishing white matter disease: an Italian case with A638G mutation in exon 5 of EIF2B2 gene, an unusual early onset and a long course. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 34: 1235-8. PMID 22729508 DOI: 10.1007/s10072-012-1129-3  0.92
2013 La Morgia C, Barboni P, Rizzo G, Carbonelli M, Savini G, Scaglione C, Capellari S, Bonazza S, Giannoccaro MP, Calandra-Buonaura G, Liguori R, Cortelli P, Martinelli P, Baruzzi A, Carelli V. Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern? European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 20: 198-201. PMID 22436028 DOI: 10.1111/j.1468-1331.2012.03701.x  0.92
2012 Cortelli P, Terlizzi R, Capellari S, Benarroch E. Nuclear lamins: functions and clinical implications. Neurology. 79: 1726-31. PMID 23071165 DOI: 10.1212/WNL.0b013e31826ea887  0.92
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  0.92
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  0.92
2012 Martinelli P, Scaglione C, Rizzo G, Capellari S. From ritual sword duel to electrophysiology: hyperactive facial motor nucleus in hemifacial spasm. Movement Disorders : Official Journal of the Movement Disorder Society. 27: 927-8. PMID 22499336 DOI: 10.1002/mds.24986  0.92
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  0.92
2011 Marconi S, Rizzo G, Capellari S, Scaglione C, Cortelli P, Martinelli P, Bonazza S. Eating disorder as a psychiatric onset of juvenile Huntington's disease. The American Journal of Psychiatry. 168: 1120-1. PMID 21969052 DOI: 10.1176/appi.ajp.2011.11020312  0.92
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  0.92
2011 Bonazza S, La Morgia C, Martinelli P, Capellari S. Strio-pallido-dentate calcinosis: a diagnostic approach in adult patients. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 32: 537-45. PMID 21479613 DOI: 10.1007/s10072-011-0514-7  0.92
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  0.92
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  0.92
2011 Guaraldi P, Donadio V, Capellari S, Contin M, Casadio MC, Montagna P, Liguori R, Cortelli P. Isolated noradrenergic failure in adult-onset autosomal dominant leukodystrophy. Autonomic Neuroscience : Basic & Clinical. 159: 123-6. PMID 20719577 DOI: 10.1016/j.autneu.2010.07.011  0.92
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  0.92
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  0.92
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  0.92
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, ... ... Capellari S, 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  0.92
2010 Fusco D, Vargiolu M, Vidone M, Mariani E, Pennisi LF, Bonora E, Capellari S, Dirnberger D, Baumeister R, Martinelli P, Romeo G. The RET51/FKBP52 complex and its involvement in Parkinson disease. Human Molecular Genetics. 19: 2804-16. PMID 20442138 DOI: 10.1093/hmg/ddq181  0.92
2010 Cevoli S, Marzocchi N, Capellari S, Scapoli C, Pierangeli G, Grimaldi D, Naldi F, Pini LA, Montagna P, Cortelli P. Lack of association between five serotonin metabolism-related genes and medication overuse headache. The Journal of Headache and Pain. 11: 53-8. PMID 19936617 DOI: 10.1007/s10194-009-0168-5  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
2009 Rizzo G, Marconi S, Capellari S, Scaglione C, Martinelli P. Benign tremulous parkinsonism in a patient with dardarin mutation. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 1399-401. PMID 19373934 DOI: 10.1002/mds.22544  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
2008 Rodríguez-Martínez AB, Alfonso-Sánchez MA, Peña JA, Sánchez-Valle R, Zerr I, Capellari S, Calero M, Zarranz JJ, de Pancorbo MM. Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation. Neurogenetics. 9: 109-18. PMID 18347820 DOI: 10.1007/s10048-008-0120-x  0.92
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  0.92
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  0.92
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  0.92
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  0.92
2005 Zaidi SI, Richardson SL, Capellari S, Song L, Smith MA, Ghetti B, Sy MS, Gambetti P, Petersen RB. Characterization of the F198S prion protein mutation: enhanced glycosylation and defective refolding. Journal of Alzheimer's Disease : Jad. 7: 159-71; discussion 1. PMID 15851854  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
2002 Taratuto AL, Piccardo P, Reich EG, Chen SG, Sevlever G, Schultz M, Luzzi AA, Rugiero M, Abecasis G, Endelman M, Garcia AM, Capellari S, Xie Z, Lugaresi E, Gambetti P, et al. Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease. Neurology. 58: 362-7. PMID 11839833  0.92
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  0.92
2001 Mastrianni JA, Capellari S, Telling GC, Han D, Bosque P, Prusiner SB, DeArmond SJ. Inherited prion disease caused by the V210I mutation: transmission to transgenic mice. Neurology. 57: 2198-205. PMID 11756597 DOI: 10.1212/WNL.57.12.2198  0.92
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  0.92
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  0.92
2000 Capellari S, Zaidi SI, Long AC, Kwon EE, Petersen RB. The Thr183Ala Mutation, Not the Loss of the First Glycosylation Site, Alters the Physical Properties of the Prion Protein. Journal of Alzheimer's Disease : Jad. 2: 27-35. PMID 12214108  0.92
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  0.92
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  0.92
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  0.92
1999 Capellari S, Zaidi SI, Urig CB, Perry G, Smith MA, Petersen RB. Prion protein glycosylation is sensitive to redox change. The Journal of Biological Chemistry. 274: 34846-50. PMID 10574957 DOI: 10.1074/jbc.274.49.34846  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
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  0.92
1994 Tinuper P, Plazzi G, Monari L, Sangiorgi S, Pellissier JF, Cerullo A, Provini F, Capellari S, Baruzzi A, Lugaresi E. Arylsulfatase A pseudodeficiency and Lafora bodies in a patient with progressive myoclonic epilepsy. Epilepsia. 35: 332-5. PMID 7908874  0.92
1992 Plazzi G, Tinuper P, Monari L, Capellari S, Sangiorgi S, Montagna P, Provini F, Cerullo A, Pellissier JF, Baruzzi A, Lugaresi E. Arylsulphatase A (ASA) pseudodeficiency (PD) and Lafora bodies (LB) in a patient with non progressive myoclonic epilepsy | EPILESSIA MIOCLONICA NON PROGRESSIVA CON CORPI DI LAFORA E PSEUDODEFICIENZA DI ARILSULFATASI A Bollettino - Lega Italiana Contro L'Epilessia. 195-196.  0.92
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