Hayashi YK - Search Results

1

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. Neuromuscul Disord. 2001 May;11(4):350-9. doi: 10.1016/s0960-8966(00)00203-0. Neuromuscul Disord. 2001. PMID: 11369186

2

A carrier of Duchenne muscular dystrophy with dilated cardiomyopathy but no skeletal muscle symptom.

Kinoshita H, Goto Y, Ishikawa M, Uemura T, Matsumoto K, Hayashi YK, Arahata K, Nonaka I. Kinoshita H, et al. Among authors: hayashi yk. Brain Dev. 1995 May-Jun;17(3):202-5. doi: 10.1016/0387-7604(95)00018-7. Brain Dev. 1995. PMID: 7573761 Review.

3

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. Muscle Nerve. 1995 Sep;18(9):1027-30. doi: 10.1002/mus.880180918. Muscle Nerve. 1995. PMID: 7643867 No abstract available.

4

The frequency of patients with 50-kd dystrophin-associated glycoprotein (50DAG or adhalin) deficiency in a muscular dystrophy patient population in Japan: immunocytochemical analysis of 50DAG, 43DAG, dystrophin, and utrophin.

Hayashi YK, Mizuno Y, Yoshida M, Nonaka I, Ozawa E, Arahata K. Hayashi YK, et al. Neurology. 1995 Mar;45(3 Pt 1):551-4. doi: 10.1212/wnl.45.3.551. Neurology. 1995. PMID: 7898714

5

Selective defect of sarcoglycan complex in severe childhood autosomal recessive muscular dystrophy muscle.

Mizuno Y, Noguchi S, Yamamoto H, Yoshida M, Suzuki A, Hagiwara Y, Hayashi YK, Arahata K, Nonaka I, Hirai S, et al. Mizuno Y, et al. Among authors: hayashi yk. Biochem Biophys Res Commun. 1994 Sep 15;203(2):979-83. doi: 10.1006/bbrc.1994.2278. Biochem Biophys Res Commun. 1994. PMID: 8093083

6

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. Among authors: hayashi yk. Lancet. 1993 Sep 4;342(8871):623-4. doi: 10.1016/0140-6736(93)91454-t. Lancet. 1993. PMID: 8102757 No abstract available.

7

Abnormal localization of laminin subunits in muscular dystrophies.

Hayashi YK, Engvall E, Arikawa-Hirasawa E, Goto K, Koga R, Nonaka I, Sugita H, Arahata K. Hayashi YK, et al. J Neurol Sci. 1993 Oct;119(1):53-64. doi: 10.1016/0022-510x(93)90191-z. J Neurol Sci. 1993. PMID: 8246011

8

Congenital muscular dystrophies.

Arahata K, Ishii H, Hayashi YK. Arahata K, et al. Among authors: hayashi yk. Curr Opin Neurol. 1995 Oct;8(5):385-90. doi: 10.1097/00019052-199510000-00011. Curr Opin Neurol. 1995. PMID: 8542045 Review.

9

Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophy.

Nagano A, Koga R, Ogawa M, Kurano Y, Kawada J, Okada R, Hayashi YK, Tsukahara T, Arahata K. Nagano A, et al. Among authors: hayashi yk. Nat Genet. 1996 Mar;12(3):254-9. doi: 10.1038/ng0396-254. Nat Genet. 1996. PMID: 8589715

10

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. Lancet. 1997 Apr 19;349(9059):1147. doi: 10.1016/S0140-6736(05)63023-1. Lancet. 1997. PMID: 9113020 No abstract available.

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