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Diagnostic accuracy of cerebrospinal fluid biomarkers in genetic prion diseases.
Schmitz M, Villar-Piqué A, Hermann P, Escaramís G, Calero M, Chen C, Kruse N, Cramm M, Golanska E, Sikorska B, Liberski PP, Pocchiari M, Lange P, Stehmann C, Sarros S, Martí E, Baldeiras I, Santana I, Žáková D, Mitrová E, Dong XP, Collins S, Poleggi A, Ladogana A, Mollenhauer B, Kovacs GG, Geschwind MD, Sánchez-Valle R, Zerr I, Llorens F. Schmitz M, et al. Among authors: geschwind md. Brain. 2022 Apr 18;145(2):700-712. doi: 10.1093/brain/awab350. Brain. 2022. PMID: 35288744 Free PMC article.
Diagnosis of human prion disease.
Safar JG, Geschwind MD, Deering C, Didorenko S, Sattavat M, Sanchez H, Serban A, Vey M, Baron H, Giles K, Miller BL, Dearmond SJ, Prusiner SB. Safar JG, et al. Among authors: geschwind md. Proc Natl Acad Sci U S A. 2005 Mar 1;102(9):3501-6. doi: 10.1073/pnas.0409651102. Proc Natl Acad Sci U S A. 2005. PMID: 15741275 Free PMC article.
First symptom in sporadic Creutzfeldt-Jakob disease.
Rabinovici GD, Wang PN, Levin J, Cook L, Pravdin M, Davis J, DeArmond SJ, Barbaro NM, Martindale J, Miller BL, Geschwind MD. Rabinovici GD, et al. Among authors: geschwind md. Neurology. 2006 Jan 24;66(2):286-7. doi: 10.1212/01.wnl.0000196440.00297.67. Neurology. 2006. PMID: 16434680 No abstract available.
Anti-GAD antibody cerebellar ataxia mimicking Creutzfeldt-Jakob disease.
Chang CC, Eggers SD, Johnson JK, Haman A, Miller BL, Geschwind MD. Chang CC, et al. Among authors: geschwind md. Clin Neurol Neurosurg. 2007 Jan;109(1):54-7. doi: 10.1016/j.clineuro.2006.01.009. Epub 2006 Apr 18. Clin Neurol Neurosurg. 2007. PMID: 16621241
Amyloid imaging in distinguishing atypical prion disease from Alzheimer disease.
Boxer AL, Rabinovici GD, Kepe V, Goldman J, Furst AJ, Huang SC, Baker SL, O'neil JP, Chui H, Geschwind MD, Small GW, Barrio JR, Jagust W, Miller BL. Boxer AL, et al. Among authors: geschwind md. Neurology. 2007 Jul 17;69(3):283-90. doi: 10.1212/01.wnl.0000265815.38958.b6. Neurology. 2007. PMID: 17636066
Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series.
Webb TE, Poulter M, Beck J, Uphill J, Adamson G, Campbell T, Linehan J, Powell C, Brandner S, Pal S, Siddique D, Wadsworth JD, Joiner S, Alner K, Petersen C, Hampson S, Rhymes C, Treacy C, Storey E, Geschwind MD, Nemeth AH, Wroe S, Collinge J, Mead S. Webb TE, et al. Among authors: geschwind md. Brain. 2008 Oct;131(Pt 10):2632-46. doi: 10.1093/brain/awn202. Epub 2008 Aug 30. Brain. 2008. PMID: 18757886 Free PMC article.
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein.
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, Dickson D, Honig L, Torres JM, Mastrianni J, Capellari S, Giaccone G, Belay ED, Schonberger LB, Cohen M, Perry G, Kong Q, Parchi P, Tagliavini F, Gambetti P. Zou WQ, et al. Ann Neurol. 2010 Aug;68(2):162-72. doi: 10.1002/ana.22094. Ann Neurol. 2010. PMID: 20695009 Free PMC article.
186 results