Arahata K - Search Results

1

A benign allelic form of laminin alpha 2 chain deficient muscular dystrophy.

Hayashi YK, Ishihara T, Domen K, Hori H, Arahata K. Hayashi YK, et al. Among authors: arahata k. Lancet. 1997 Apr 19;349(9059):1147. doi: 10.1016/S0140-6736(05)63023-1. Lancet. 1997. PMID: 9113020 No abstract available.

2

Deficiency of laminin alpha 2-chain mRNA in muscle in a patient with merosin-negative congenital muscular dystrophy.

Hayashi YK, Koga R, Tsukahara T, Ishii H, Matsuishi T, Yamashita Y, Nonaka I, Arahata K. Hayashi YK, et al. Among authors: arahata k. Muscle Nerve. 1995 Sep;18(9):1027-30. doi: 10.1002/mus.880180918. Muscle Nerve. 1995. PMID: 7643867 No abstract available.

3

[Congenital muscular dystrophy (CMD)].

Hayashi YK, Arahata K. Hayashi YK, et al. Among authors: arahata k. No To Shinkei. 1997 Apr;49(4):311-8. No To Shinkei. 1997. PMID: 9125738 Review. Japanese. No abstract available.

4

Congenital muscular dystrophy: Clinical and pathologic study of 50 patients with the classical (Occidental) merosin-positive form.

Kobayashi O, Hayashi Y, Arahata K, Ozawa E, Nonaka I. Kobayashi O, et al. Among authors: arahata k. Neurology. 1996 Mar;46(3):815-8. doi: 10.1212/wnl.46.3.815. Neurology. 1996. PMID: 8618689

5

Dystrophin-associated glycoprotein and dystrophin co-localisation at sarcolemma in Fukuyama congenital muscular dystrophy.

Arahata K, Hayashi YK, Mizuno Y, Yoshida M, Ozawa M. Arahata K, et al. Lancet. 1993 Sep 4;342(8871):623-4. doi: 10.1016/0140-6736(93)91454-t. Lancet. 1993. PMID: 8102757 No abstract available.

6

Laminin alpha2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)-deficient congenital muscular dystrophy.

Miyagoe Y, Hanaoka K, Nonaka I, Hayasaka M, Nabeshima Y, Arahata K, Nabeshima Y, Takeda S. Miyagoe Y, et al. Among authors: arahata k. FEBS Lett. 1997 Sep 22;415(1):33-9. doi: 10.1016/s0014-5793(97)01007-7. FEBS Lett. 1997. PMID: 9326364 Free article.

7

Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophy.

Hayashi YK, Tezak Z, Momoi T, Nonaka I, Garcia CA, Hoffman EP, Arahata K. Hayashi YK, et al. Among authors: arahata k. Neuromuscul Disord. 2001 May;11(4):350-9. doi: 10.1016/s0960-8966(00)00203-0. Neuromuscul Disord. 2001. PMID: 11369186

8

Muscular dystrophy.

Arahata K. Arahata K. Neuropathology. 2000 Sep;20 Suppl:S34-41. doi: 10.1046/j.1440-1789.2000.00321.x. Neuropathology. 2000. PMID: 11037185 Review.

9

Mosaic expression of dystrophin in symptomatic carriers of Duchenne's muscular dystrophy.

Arahata K, Ishihara T, Kamakura K, Tsukahara T, Ishiura S, Baba C, Matsumoto T, Nonaka I, Sugita H. Arahata K, et al. N Engl J Med. 1989 Jan 19;320(3):138-42. doi: 10.1056/NEJM198901193200302. N Engl J Med. 1989. PMID: 2643040

10

[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.

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