Fukazawa T - Search Results

1

Spinocerebellar ataxia type 1 and familial spontaneous pneumothorax.

Fukazawa T, Sasaki H, Kikuchi S, Hamada K, Hamada T, Tashiro K. Fukazawa T, et al. Neurology. 1997 Nov;49(5):1460-2. doi: 10.1212/wnl.49.5.1460. Neurology. 1997. PMID: 9371943

2

Spinocerebellar ataxia 1 (SCA1) in the Japanese in Hokkaido may derive from a single common ancestry.

Wakisaka A, Sasaki H, Takada A, Fukazawa T, Suzuki Y, Hamada T, Iwabuchi K, Tashiro K, Yoshiki T. Wakisaka A, et al. Among authors: fukazawa t. J Med Genet. 1995 Aug;32(8):590-2. doi: 10.1136/jmg.32.8.590. J Med Genet. 1995. PMID: 7473647 Free PMC article.

3

Spinocerebellar ataxia 1 (SCA1) in the Japanese: analysis of CAG trinucleitide repeat expansion and instability of the repeat for paternal transmission.

Suzuki Y, Sasaki H, Wakisaka A, Takada A, Yoshiki T, Iwabuchi K, Tashiro K, Fukazawa T, Hamada T. Suzuki Y, et al. Among authors: fukazawa t. Jpn J Hum Genet. 1995 Mar;40(1):131-43. doi: 10.1007/BF01874077. Jpn J Hum Genet. 1995. PMID: 7780164

4

Multifocal eosinophilic granuloma presenting as progressive brainstem and cerebellar dysfunction.

Fukazawa T, Yanagihara T, Hamada K, Hamada T. Fukazawa T, et al. J Neurol Neurosurg Psychiatry. 1994 Aug;57(8):980-2. doi: 10.1136/jnnp.57.8.980. J Neurol Neurosurg Psychiatry. 1994. PMID: 8057124 Free PMC article.

5

Clinical features and natural history of spinocerebellar ataxia type 1.

Sasaki H, Fukazawa T, Yanagihara T, Hamada T, Shima K, Matsumoto A, Hashimoto K, Ito N, Wakisaka A, Tashiro K. Sasaki H, et al. Among authors: fukazawa t. Acta Neurol Scand. 1996 Jan;93(1):64-71. doi: 10.1111/j.1600-0404.1996.tb00173.x. Acta Neurol Scand. 1996. PMID: 8825276

6

[A case of chronic bromvalerylurea intoxication with episodic neurological manifestations such as optic neuropathy ophthalmoplegia and ataxia].

Fukazawa T, Sasaki H, Ito-Owada Y, Hamada T, Tashiro K. Fukazawa T, et al. Rinsho Shinkeigaku. 1996 Jun;36(6):790-2. Rinsho Shinkeigaku. 1996. PMID: 8937204 Japanese.

7

[MRI changes in spontaneous intracranial hypotension].

Honma S, Fukazawa T, Hamada K, Hamada T, Tashiro K. Honma S, et al. Among authors: fukazawa t. Rinsho Shinkeigaku. 1996 Jul;36(7):912-5. Rinsho Shinkeigaku. 1996. PMID: 8952366 Japanese.

8

Central phenotype and related varieties of spinocerebellar ataxia 2 (SCA2): a clinical and genetic study with a pedigree in the Japanese.

Sasaki H, Fukazawa T, Wakisaka A, Hamada K, Hamada T, Koyama T, Tsuji S, Tashiro K. Sasaki H, et al. Among authors: fukazawa t. J Neurol Sci. 1996 Dec;144(1-2):176-81. doi: 10.1016/s0022-510x(96)00225-0. J Neurol Sci. 1996. PMID: 8994121 Clinical Trial.

9

Dominantly inherited leukodystrophy showing cerebellar deficits and spastic paraparesis: a new entity?

Fukazawa T, Sasaki H, Kikuchi S, Hamada K, Hamada T, Tashiro K. Fukazawa T, et al. J Neurol. 1997 Jul;244(7):446-9. doi: 10.1007/s004150050120. J Neurol. 1997. PMID: 9266464

10

Anti-nuclear antibodies and the optic-spinal form of multiple sclerosis.

Fukazawa T, Kikuchi S, Sasaki H, Hamada K, Hamada T, Miyasaka K, Tashiro K. Fukazawa T, et al. J Neurol. 1997 Aug;244(8):483-8. doi: 10.1007/s004150050129. J Neurol. 1997. PMID: 9309553

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