Tanaka H - Search Results

1

Ataxia with isolated vitamin E deficiency and retinitis pigmentosa.

Shimohata T, Date H, Ishiguro H, Suzuki T, Takano H, Tanaka H, Tsuji S, Hirota K. Shimohata T, et al. Among authors: tanaka h. Ann Neurol. 1998 Feb;43(2):273. doi: 10.1002/ana.410430222. Ann Neurol. 1998. PMID: 9485073 No abstract available.

2

Sporadic cases of dentatorubral-pallidoluysian atrophy associated with maternal transmission.

Shimohata T, Ishiguro H, Makino K, Takano H, Tanaka H, Tsuji S, Hirota K. Shimohata T, et al. Among authors: tanaka h. Neurology. 1998 Jan;50(1):282-3. doi: 10.1212/wnl.50.1.282. Neurology. 1998. PMID: 9443494

3

Spinocerebellar ataxia type 6: CAG repeat expansion in alpha1A voltage-dependent calcium channel gene and clinical variations in Japanese population.

Ikeuchi T, Takano H, Koide R, Horikawa Y, Honma Y, Onishi Y, Igarashi S, Tanaka H, Nakao N, Sahashi K, Tsukagoshi H, Inoue K, Takahashi H, Tsuji S. Ikeuchi T, et al. Among authors: tanaka h. Ann Neurol. 1997 Dec;42(6):879-84. doi: 10.1002/ana.410420609. Ann Neurol. 1997. PMID: 9403480

4

Atrophy of the cerebellum and brainstem in dentatorubral pallidoluysian atrophy. Influence of CAG repeat size on MRI findings.

Koide R, Onodera O, Ikeuchi T, Kondo R, Tanaka H, Tokiguchi S, Tomoda A, Miike T, Isa F, Beppu H, Shimizu N, Watanabe Y, Horikawa Y, Shimohata T, Hirota K, Ishikawa A, Tsuji S. Koide R, et al. Among authors: tanaka h. Neurology. 1997 Dec;49(6):1605-12. doi: 10.1212/wnl.49.6.1605. Neurology. 1997. PMID: 9409354

5

Linkage mapping of the gene for Charcot-Marie-Tooth disease type 2 to chromosome 1p (CMT2A) and the clinical features of CMT2A.

Saito M, Hayashi Y, Suzuki T, Tanaka H, Hozumi I, Tsuji S. Saito M, et al. Among authors: tanaka h. Neurology. 1997 Dec;49(6):1630-5. doi: 10.1212/wnl.49.6.1630. Neurology. 1997. PMID: 9409358

6

Progressive atrophy of cerebellum and brainstem as a function of age and the size of the expanded CAG repeats in the MJD1 gene in Machado-Joseph disease.

Onodera O, Idezuka J, Igarashi S, Takiyama Y, Endo K, Takano H, Oyake M, Tanaka H, Inuzuka T, Hayashi T, Yuasa T, Ito J, Miyatake T, Tsuji S. Onodera O, et al. Among authors: tanaka h. Ann Neurol. 1998 Mar;43(3):288-96. doi: 10.1002/ana.410430305. Ann Neurol. 1998. PMID: 9506544

7

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: tanaka h. 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

8

X-linked nonprogressive congenital cerebellar hypoplasia: clinical description and mapping to chromosome Xq.

Illarioshkin SN, Tanaka H, Markova ED, Nikolskaya NN, Ivanova-Smolenskaya IA, Tsuji S. Illarioshkin SN, et al. Among authors: tanaka h. Ann Neurol. 1996 Jul;40(1):75-83. doi: 10.1002/ana.410400113. Ann Neurol. 1996. PMID: 8687195

9

Novel mutations, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism.

Maruyama M, Ikeuchi T, Saito M, Ishikawa A, Yuasa T, Tanaka H, Hayashi S, Wakabayashi K, Takahashi H, Tsuji S. Maruyama M, et al. Among authors: tanaka h. Ann Neurol. 2000 Aug;48(2):245-50. Ann Neurol. 2000. PMID: 10939576

10

Pure cerebellar ataxia phenotype in Machado-Joseph disease.

Ishikawa K, Mizusawa H, Igarashi S, Takiyama Y, Tanaka H, Ohkoshi N, Shoji S, Tsuji S. Ishikawa K, et al. Among authors: tanaka h. Neurology. 1996 Jun;46(6):1776-7. doi: 10.1212/wnl.46.6.1776. Neurology. 1996. PMID: 8649595 No abstract available.

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