Arahata K - 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. 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

2

Presence of emerinopathy in cases of rigid spine syndrome.

Kubo S, Tsukahara T, Takemitsu M, Yoon KB, Utsumi H, Nonaka I, Arahata K. Kubo S, et al. Among authors: arahata k. Neuromuscul Disord. 1998 Oct;8(7):502-7. doi: 10.1016/s0960-8966(98)00069-8. Neuromuscul Disord. 1998. PMID: 9829281

3

Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy.

Hayashi YK, Ogawa M, Tagawa K, Noguchi S, Ishihara T, Nonaka I, Arahata K. Hayashi YK, et al. Among authors: arahata k. Neurology. 2001 Jul 10;57(1):115-21. doi: 10.1212/wnl.57.1.115. Neurology. 2001. PMID: 11445638

4

A severe muscular dystrophy patient with an internally deleted very short (110 kD) dystrophin: presence of the binding site for dystrophin-associated glycoprotein (DAG) may not be enough for physiological function of dystrophin.

Arikawa-Hirasawa E, Koga R, Tsukahara T, Nonaka I, Mitsudome A, Goto K, Beggs AH, Arahata K. Arikawa-Hirasawa E, et al. Among authors: arahata k. Neuromuscul Disord. 1995 Sep;5(5):429-38. doi: 10.1016/0960-8966(94)00087-p. Neuromuscul Disord. 1995. PMID: 7496177

5

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: arahata k. Brain Dev. 1995 May-Jun;17(3):202-5. doi: 10.1016/0387-7604(95)00018-7. Brain Dev. 1995. PMID: 7573761 Review.

6

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.

7

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. Among authors: arahata k. Neurology. 1995 Mar;45(3 Pt 1):551-4. doi: 10.1212/wnl.45.3.551. Neurology. 1995. PMID: 7898714

8

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: arahata k. Biochem Biophys Res Commun. 1994 Sep 15;203(2):979-83. doi: 10.1006/bbrc.1994.2278. Biochem Biophys Res Commun. 1994. PMID: 8093083

9

Congenital muscular dystrophies.

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

10

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

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