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1,074 results
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Redefining cerebellar ataxia in degenerative ataxias: lessons from recent research on cerebellar systems.
Tada M, Nishizawa M, Onodera O. Tada M, et al. Among authors: nishizawa m. J Neurol Neurosurg Psychiatry. 2015 Aug;86(8):922-8. doi: 10.1136/jnnp-2013-307225. Epub 2015 Jan 30. J Neurol Neurosurg Psychiatry. 2015. PMID: 25637456 Review.
Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1.
Ishikawa K, Tanaka H, Saito M, Ohkoshi N, Fujita T, Yoshizawa K, Ikeuchi T, Watanabe M, Hayashi A, Takiyama Y, Nishizawa M, Nakano I, Matsubayashi K, Miwa M, Shoji S, Kanazawa I, Tsuji S, Mizusawa H. Ishikawa K, et al. Among authors: nishizawa m. Am J Hum Genet. 1997 Aug;61(2):336-46. doi: 10.1086/514867. Am J Hum Genet. 1997. PMID: 9311738 Free PMC article.
A novel locus for dominant cerebellar ataxia (SCA14) maps to a 10.2-cM interval flanked by D19S206 and D19S605 on chromosome 19q13.4-qter.
Yamashita I, Sasaki H, Yabe I, Fukazawa T, Nogoshi S, Komeichi K, Takada A, Shiraishi K, Takiyama Y, Nishizawa M, Kaneko J, Tanaka H, Tsuji S, Tashiro K. Yamashita I, et al. Among authors: nishizawa m. Ann Neurol. 2000 Aug;48(2):156-63. doi: 10.1002/1531-8249(200008)48:2<156::aid-ana4>3.0.co;2-9. Ann Neurol. 2000. PMID: 10939565
Dysferlin mutations in Japanese Miyoshi myopathy: relationship to phenotype.
Takahashi T, Aoki M, Tateyama M, Kondo E, Mizuno T, Onodera Y, Takano R, Kawai H, Kamakura K, Mochizuki H, Shizuka-Ikeda M, Nakagawa M, Yoshida Y, Akanuma J, Hoshino K, Saito H, Nishizawa M, Kato S, Saito K, Miyachi T, Yamashita H, Kawai M, Matsumura T, Kuzuhara S, Ibi T, Sahashi K, Nakai H, Kohnosu T, Nonaka I, Arahata K, Brown RH Jr, Saito H, Itoyama Y. Takahashi T, et al. Among authors: nishizawa m. Neurology. 2003 Jun 10;60(11):1799-804. doi: 10.1212/01.wnl.0000068333.43005.12. Neurology. 2003. PMID: 12796534
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: nishizawa m. Neurology. 2004 Jan 13;62(1):107-9. doi: 10.1212/01.wnl.0000099371.14478.73. Neurology. 2004. PMID: 14718708
Quantitative evaluation of brainstem involvement in multiple system atrophy by diffusion-weighted MR imaging.
Kanazawa M, Shimohata T, Terajima K, Onodera O, Tanaka K, Tsuji S, Okamoto K, Nishizawa M. Kanazawa M, et al. Among authors: nishizawa m. J Neurol. 2004 Sep;251(9):1121-4. doi: 10.1007/s00415-004-0494-0. J Neurol. 2004. PMID: 15372256
Sacsin-related autosomal recessive ataxia without prominent retinal myelinated fibers in Japan.
Hara K, Onodera O, Endo M, Kondo H, Shiota H, Miki K, Tanimoto N, Kimura T, Nishizawa M. Hara K, et al. Among authors: nishizawa m. Mov Disord. 2005 Mar;20(3):380-2. doi: 10.1002/mds.20315. Mov Disord. 2005. PMID: 15486997
New HSN2 mutation in Japanese patient with hereditary sensory and autonomic neuropathy type 2.
Takagi M, Ozawa T, Hara K, Naruse S, Ishihara T, Shimbo J, Igarashi S, Tanaka K, Onodera O, Nishizawa M. Takagi M, et al. Among authors: nishizawa m. Neurology. 2006 Apr 25;66(8):1251-2. doi: 10.1212/01.wnl.0000208415.90685.cd. Neurology. 2006. PMID: 16636245
A possible variant of neuro-Beh├žet disease presenting chronic progressive ataxia without mucocutaneo-ocular symptoms.
Hirose M, Ikeuchi T, Hayashi S, Terajima K, Endo K, Hayashi T, Kakita A, Kimura T, Takahashi H, Nishizawa M. Hirose M, et al. Among authors: nishizawa m. Rheumatol Int. 2006 Nov;27(1):61-5. doi: 10.1007/s00296-006-0171-y. Epub 2006 Aug 25. Rheumatol Int. 2006. PMID: 16932965
Early development of autonomic dysfunction may predict poor prognosis in patients with multiple system atrophy.
Tada M, Onodera O, Tada M, Ozawa T, Piao YS, Kakita A, Takahashi H, Nishizawa M. Tada M, et al. Among authors: nishizawa m. Arch Neurol. 2007 Feb;64(2):256-60. doi: 10.1001/archneur.64.2.256. Arch Neurol. 2007. PMID: 17296842
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