Sahashi K - Search Results

1

Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophy.

Igarashi S, Tanno Y, Onodera O, Yamazaki M, Sato S, Ishikawa A, Miyatani N, Nagashima M, Ishikawa Y, Sahashi K, et al. Igarashi S, et al. Among authors: sahashi k. Neurology. 1992 Dec;42(12):2300-2. doi: 10.1212/wnl.42.12.2300. Neurology. 1992. PMID: 1461383

2

[A mother and her son with autosomal dominant bulbar spinal muscular atrophy].

Ibi T, Suoh H, Igarashi S, Tsuji S, Sahashi K. Ibi T, et al. Among authors: sahashi k. Rinsho Shinkeigaku. 1992 Sep;32(9):1038-40. Rinsho Shinkeigaku. 1992. PMID: 1300263 Japanese.

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: sahashi k. Ann Neurol. 1997 Dec;42(6):879-84. doi: 10.1002/ana.410420609. Ann Neurol. 1997. PMID: 9403480

4

[Computed tomographic analyses on skeletal muscles in bulbar spinal muscular atrophy].

Koga H, Yamamoto H, Sahashi K, Ibi T, Mori K. Koga H, et al. Among authors: sahashi k. Rinsho Shinkeigaku. 1990 Aug;30(8):828-34. Rinsho Shinkeigaku. 1990. PMID: 2253416 Japanese.

5

Mitochondrial DNA deletions in inherited recurrent myoglobinuria.

Ohno K, Tanaka M, Sahashi K, Ibi T, Sato W, Yamamoto T, Takahashi A, Ozawa T. Ohno K, et al. Among authors: sahashi k. Ann Neurol. 1991 Apr;29(4):364-9. doi: 10.1002/ana.410290406. Ann Neurol. 1991. PMID: 1929207

6

Direct DNA sequencing from colony: analysis of multiple deletions of mitochondrial genome.

Ohno K, Tanaka M, Ino H, Suzuki H, Tashiro M, Ibi T, Sahashi K, Takahashi A, Ozawa T. Ohno K, et al. Among authors: sahashi k. Biochim Biophys Acta. 1991 Aug 27;1090(1):9-16. doi: 10.1016/0167-4781(91)90030-p. Biochim Biophys Acta. 1991. PMID: 1832017

7

Type I familial amyloid polyneuropathy. A pathological study of the peripheral nervous system.

Sobue G, Nakao N, Murakami K, Yasuda T, Sahashi K, Mitsuma T, Sasaki H, Sakaki Y, Takahashi A. Sobue G, et al. Among authors: sahashi k. Brain. 1990 Aug;113 ( Pt 4):903-19. doi: 10.1093/brain/113.4.903. Brain. 1990. PMID: 2168781

8

Progressive myopathy with circulating autoantibody against giantin in the Golgi apparatus.

Sahashi K, Ibi T, Ohno K, Sahashi K, Nakao N, Kondo H. Sahashi K, et al. Neurology. 2004 May 25;62(10):1891-3. doi: 10.1212/01.wnl.0000125253.84724.b8. Neurology. 2004. PMID: 15159505

9

Cytoplasmic body and mitochondrial DNA deletion.

Sahashi K, Ohno K, Tanaka M, Ibi T, Yamamoto T, Tashiro M, Sato W, Takahashi A, Ozawa T. Sahashi K, et al. J Neurol Sci. 1990 Nov;99(2-3):291-300. doi: 10.1016/0022-510x(90)90163-h. J Neurol Sci. 1990. PMID: 1964959

10

Degenerating compartment and functioning compartment of motor neurons in ALS: possible process of motor neuron loss.

Sobue G, Sahashi K, Takahashi A, Matsuoka Y, Muroga T, Sobue I. Sobue G, et al. Among authors: sahashi k. Neurology. 1983 May;33(5):654-7. doi: 10.1212/wnl.33.5.654. Neurology. 1983. PMID: 6682506

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