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Paraneoplastic anti-N-methyl-D-aspartate receptor encephalitis associated with ovarian teratoma.
Dalmau J, Tüzün E, Wu HY, Masjuan J, Rossi JE, Voloschin A, Baehring JM, Shimazaki H, Koide R, King D, Mason W, Sansing LH, Dichter MA, Rosenfeld MR, Lynch DR. Dalmau J, et al. Among authors: Shimazaki H. Ann Neurol. 2007 Jan;61(1):25-36. doi: 10.1002/ana.21050. Ann Neurol. 2007. PMID: 17262855 Free PMC article. Clinical Trial.
Identification of GFAP gene mutation in hereditary adult-onset Alexander's disease.
Namekawa M, Takiyama Y, Aoki Y, Takayashiki N, Sakoe K, Shimazaki H, Taguchi T, Tanaka Y, Nishizawa M, Saito K, Matsubara Y, Nakano I. Namekawa M, et al. Among authors: Shimazaki H. Ann Neurol. 2002 Dec;52(6):779-85. doi: 10.1002/ana.10375. Ann Neurol. 2002. PMID: 12447932
Identification of a SACS gene missense mutation in ARSACS.
Ogawa T, Takiyama Y, Sakoe K, Mori K, Namekawa M, Shimazaki H, Nakano I, Nishizawa M. Ogawa T, et al. Among authors: Shimazaki H. Neurology. 2004 Jan 13;62(1):107-9. doi: 10.1212/01.wnl.0000099371.14478.73. Neurology. 2004. PMID: 14718708
A phenotype without spasticity in sacsin-related ataxia.
Shimazaki H, Takiyama Y, Sakoe K, Ando Y, Nakano I. Shimazaki H, et al. Neurology. 2005 Jun 28;64(12):2129-31. doi: 10.1212/01.WNL.0000166031.91514.B3. Neurology. 2005. PMID: 15985586
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