Hirota K - 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: hirota k. 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: hirota k. Neurology. 1998 Jan;50(1):282-3. doi: 10.1212/wnl.50.1.282. Neurology. 1998. PMID: 9443494

3

Japanese SCA families with an unusual phenotype linked to a locus overlapping with SCA15 locus.

Hara K, Fukushima T, Suzuki T, Shimohata T, Oyake M, Ishiguro H, Hirota K, Miyashita A, Kuwano R, Kurisaki H, Yomono H, Goto J, Kanazawa I, Tsuji S. Hara K, et al. Among authors: hirota k. Neurology. 2004 Feb 24;62(4):648-51. doi: 10.1212/01.wnl.0000110190.08412.25. Neurology. 2004. PMID: 14981189

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: hirota k. Neurology. 1997 Dec;49(6):1605-12. doi: 10.1212/wnl.49.6.1605. Neurology. 1997. PMID: 9409354

5

[Adult onset Still's disease with a brainstem lesion demonstrated on MRI].

Shimohata T, Ishiguro H, Hirota K. Shimohata T, et al. Among authors: hirota k. Rinsho Shinkeigaku. 1997 May;37(5):379-82. Rinsho Shinkeigaku. 1997. PMID: 9294323 Japanese.

6

Cerebral vasculopathy showing moyamoya-like changes in a patient with CREST syndrome.

Terajima K, Shimohata T, Watanabe M, Suzuki T, Hasegawa A, Ishiguro H, Minakawa T, Hirota K. Terajima K, et al. Among authors: hirota k. Eur Neurol. 2001;46(3):163-5. doi: 10.1159/000050795. Eur Neurol. 2001. PMID: 11598340 No abstract available.

7

Pontine atrophy in spinocerebellar ataxia type 6.

Sugawara M, Toyoshima I, Wada C, Kato K, Ishikawa K, Hirota K, Ishiguro H, Kagaya H, Hirata Y, Imota T, Ogasawara M, Masamune O. Sugawara M, et al. Among authors: hirota k. Eur Neurol. 2000;43(1):17-22. doi: 10.1159/000008123. Eur Neurol. 2000. PMID: 10601803

8

Nigral degeneration in a case of amyotrophic lateral sclerosis: evidence of Lewy body-like and skein-like inclusions in the pigmented neurons.

Su M, Yoshida Y, Ishiguro H, Hirota K. Su M, et al. Among authors: hirota k. Clin Neuropathol. 1999 Nov-Dec;18(6):293-300. Clin Neuropathol. 1999. PMID: 10580555

9

[Hereditary ataxias in Akita prefecture].

Sugawara M, Toyoshima I, Kato K, Wada C, Imota T, Hirota K, Ishiguro H, Kagaya H, Hirata A, Ogasawara M, Masamune O. Sugawara M, et al. Among authors: hirota k. Rinsho Shinkeigaku. 1999 Jul;39(7):763-6. Rinsho Shinkeigaku. 1999. PMID: 10548917 Japanese.

10

Pressure sintering of apatite-collagen composite.

Hirota K, Nishihara K, Tanaka H. Hirota K, et al. Biomed Mater Eng. 1993 Fall;3(3):147-51. Biomed Mater Eng. 1993. PMID: 8193566

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