Sahashi KO - Search Results

1

Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD).

Lee JH, Goto K, Sahashi KO, Nonaka I, Matsuda C, Arahata K. Lee JH, et al. Among authors: sahashi ko. Muscle Nerve Suppl. 1995;(2):S27-31. Muscle Nerve Suppl. 1995. PMID: 23573583

2

DNA rearrangements in Japanese facioscapulohumeral muscular dystrophy patients: clinical correlations.

Goto K, Lee JH, Matsuda C, Hirabayashi K, Kojo T, Nakamura A, Mitsunaga Y, Furukawa T, Sahashi K, Arahata K. Goto K, et al. Neuromuscul Disord. 1995 May;5(3):201-8. doi: 10.1016/0960-8966(94)00055-e. Neuromuscul Disord. 1995. PMID: 7633185

3

Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD).

Lee JH, Goto K, Sahashi K, Nonaka I, Matsuda C, Arahata K. Lee JH, et al. Muscle Nerve Suppl. 1995;2:S27-31. Muscle Nerve Suppl. 1995. PMID: 7739622

4

Multiplicity of abnormal dystrophin in Becker muscular dystrophy. A Becker muscular dystrophy gene frequently produced two smaller sizes of dystrophin.

Hori S, Ohtani S, Shimizu T, Ibi T, Sahashi K, Nonaka I, Miyamoto K, Tanabe H. Hori S, et al. J Neurol Sci. 1994 Feb;121(2):183-9. doi: 10.1016/0022-510x(94)90350-6. J Neurol Sci. 1994. PMID: 8158213

5

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. Neurology. 2003 Jun 10;60(11):1799-804. doi: 10.1212/01.wnl.0000068333.43005.12. Neurology. 2003. PMID: 12796534

6

A sodium channel myotonia due to a novel SCN4A mutation accompanied by acquired autoimmune myasthenia gravis.

Kokunai Y, Goto K, Kubota T, Fukuoka T, Sakoda S, Ibi T, Doyu M, Mochizuki H, Sahashi K, Takahashi MP. Kokunai Y, et al. Among authors: sahashi k. Neurosci Lett. 2012 Jun 21;519(1):67-72. doi: 10.1016/j.neulet.2012.05.023. Epub 2012 May 14. Neurosci Lett. 2012. PMID: 22617007

7

Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population.

Nozaki H, Ikeuchi T, Kawakami A, Kimura A, Koide R, Tsuchiya M, Nakmura Y, Mutoh T, Yamamoto H, Nakao N, Sahashi K, Nishizawa M, Onodera O. Nozaki H, et al. Among authors: sahashi k. Mov Disord. 2007 Apr 30;22(6):857-62. doi: 10.1002/mds.21443. Mov Disord. 2007. PMID: 17357132

8

[Biochemical and histochemical studies on platelet serotonin of Duchenne muscular dystrophy--A new approach for carrier detection].

Fukunaga H, Hori S, Sahashi K, Uono M. Fukunaga H, et al. Rinsho Shinkeigaku. 1977 May;17(5):316-21. Rinsho Shinkeigaku. 1977. PMID: 560278 Japanese. No abstract available.

9

[Compound heterozygous mutations in the muscle chloride channel gene (CLCN1) in a Japanese family with Thomsen's disease].

Sasaki R, Takahashi MP, Kokunai Y, Hirayama M, Ibi T, Tomimoto H, Mochizuki H, Sahashi K. Sasaki R, et al. Among authors: sahashi k. Rinsho Shinkeigaku. 2013;53(4):316-9. doi: 10.5692/clinicalneurol.53.316. Rinsho Shinkeigaku. 2013. PMID: 23603549 Japanese.

10

[Myasthenia gravis, giant cell polymyositis and cardiomyositis associated with thymoma].

Ibi T, Sahashi K. Ibi T, et al. Ryoikibetsu Shokogun Shirizu. 2001;(36):344-6. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11596405 Review. Japanese. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

62 results

Search Page

Filters