Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

193 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
[Muscular dystrophy].
Tsukahara T, Ishiura S, Arahata K, Sugita H. Tsukahara T, et al. Among authors: arahata k. Tanpakushitsu Kakusan Koso. 1990 May;35(7 Suppl):1246-53. Tanpakushitsu Kakusan Koso. 1990. PMID: 2192396 Japanese. No abstract available.
Quadriceps myopathy: forme fruste of Becker muscular dystrophy.
Sunohara N, Arahata K, Hoffman EP, Yamada H, Nishimiya J, Arikawa E, Kaido M, Nonaka I, Sugita H. Sunohara N, et al. Among authors: arahata k. Ann Neurol. 1990 Nov;28(5):634-9. doi: 10.1002/ana.410280506. Ann Neurol. 1990. PMID: 2260849
[Cardiomyopathy in Becker muscular dystrophy].
Sakata C, Yamada H, Sunohara N, Arahata K, Nonaka I. Sakata C, et al. Among authors: arahata k. Rinsho Shinkeigaku. 1990 Sep;30(9):952-5. Rinsho Shinkeigaku. 1990. PMID: 2265504 Japanese.
Muscle histology in Becker muscular dystrophy.
Kaido M, Arahata K, Hoffman EP, Nonaka I, Sugita H. Kaido M, et al. Among authors: arahata k. Muscle Nerve. 1991 Nov;14(11):1067-73. doi: 10.1002/mus.880141105. Muscle Nerve. 1991. PMID: 1745279
Mutation in the caveolin-3 gene causes a peculiar form of distal myopathy.
Tateyama M, Aoki M, Nishino I, Hayashi YK, Sekiguchi S, Shiga Y, Takahashi T, Onodera Y, Haginoya K, Kobayashi K, Iinuma K, Nonaka I, Arahata K, Itoyama Y. Tateyama M, et al. Among authors: arahata k. Neurology. 2002 Jan 22;58(2):323-5. doi: 10.1212/wnl.58.2.323. Neurology. 2002. PMID: 11805270
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. Among authors: arahata k. Neurology. 2003 Jun 10;60(11):1799-804. doi: 10.1212/01.wnl.0000068333.43005.12. Neurology. 2003. PMID: 12796534
193 results