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Expanding the global prevalence of spinocerebellar ataxia type 42.
Ngo K, Aker M, Petty LE, Chen J, Cavalcanti F, Nelson AB, Hassin-Baer S, Geschwind MD, Perlman S, Italiano D, Laganà A, Cavallaro S, Coppola G, Below JE, Fogel BL. Ngo K, et al. Neurol Genet. 2018 Apr 5;4(3):e232. doi: 10.1212/NXG.0000000000000232. eCollection 2018 Jun. Neurol Genet. 2018. PMID: 29629410 Free PMC article. No abstract available.
PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations.
Hatano Y, Sato K, Elibol B, Yoshino H, Yamamura Y, Bonifati V, Shinotoh H, Asahina M, Kobayashi S, Ng AR, Rosales RL, Hassin-Baer S, Shinar Y, Lu CS, Chang HC, Wu-Chou YH, Ataç FB, Kobayashi T, Toda T, Mizuno Y, Hattori N. Hatano Y, et al. Neurology. 2004 Oct 26;63(8):1482-5. doi: 10.1212/01.wnl.0000142258.29304.fe. Neurology. 2004. PMID: 15505170
Stiff-person syndrome following West Nile fever.
Hassin-Baer S, Kirson ED, Shulman L, Buchman AS, Bin H, Hindiyeh M, Markevich L, Mendelson E. Hassin-Baer S, et al. Arch Neurol. 2004 Jun;61(6):938-41. doi: 10.1001/archneur.61.6.938. Arch Neurol. 2004. PMID: 15210535
Novel PINK1 mutations in early-onset parkinsonism.
Hatano Y, Li Y, Sato K, Asakawa S, Yamamura Y, Tomiyama H, Yoshino H, Asahina M, Kobayashi S, Hassin-Baer S, Lu CS, Ng AR, Rosales RL, Shimizu N, Toda T, Mizuno Y, Hattori N. Hatano Y, et al. Ann Neurol. 2004 Sep;56(3):424-7. doi: 10.1002/ana.20251. Ann Neurol. 2004. PMID: 15349870
148 results