Nonaka I - Search Results

1

Molecular pathomechanism of distal myopathy with rimmed vacuoles.

Nishino I, Malicdan MC, Murayama K, Nonaka I, Hayashi YK, Noguchi S. Nishino I, et al. Among authors: nonaka i. Acta Myol. 2005 Oct;24(2):80-3. Acta Myol. 2005. PMID: 16550921 Review.

2

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy.

Noguchi S, McNally EM, Ben Othmane K, Hagiwara Y, Mizuno Y, Yoshida M, Yamamoto H, Bönnemann CG, Gussoni E, Denton PH, Kyriakides T, Middleton L, Hentati F, Ben Hamida M, Nonaka I, Vance JM, Kunkel LM, Ozawa E. Noguchi S, et al. Among authors: nonaka i. Science. 1995 Nov 3;270(5237):819-22. doi: 10.1126/science.270.5237.819. Science. 1995. PMID: 7481775

3

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

4

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

5

Reducing bodies in distal myopathy with rimmed vacuole formation.

Kiyomoto BH, Murakami N, Kishibayashi J, Sunohara N, Nonaka I. Kiyomoto BH, et al. Among authors: nonaka i. Acta Neuropathol. 1995;89(1):109-11. doi: 10.1007/BF00294268. Acta Neuropathol. 1995. PMID: 7709723

6

Muscle fiber degeneration in distal myopathy with rimmed vacuole formation.

Murakami N, Ihara Y, Nonaka I. Murakami N, et al. Among authors: nonaka i. Acta Neuropathol. 1995;89(1):29-34. doi: 10.1007/BF00294256. Acta Neuropathol. 1995. PMID: 7709728

7

Sarcoglycan complex is selectively lost in dystrophic hamster muscle.

Mizuno Y, Noguchi S, Yamamoto H, Yoshida M, Nonaka I, Hirai S, Ozawa E. Mizuno Y, et al. Among authors: nonaka i. Am J Pathol. 1995 Feb;146(2):530-6. Am J Pathol. 1995. PMID: 7856762 Free PMC article.

8

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: nonaka i. Neurology. 1995 Mar;45(3 Pt 1):551-4. doi: 10.1212/wnl.45.3.551. Neurology. 1995. PMID: 7898714

9

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

10

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. Among authors: nonaka i. J Neurol Sci. 1993 Oct;119(1):53-64. doi: 10.1016/0022-510x(93)90191-z. J Neurol Sci. 1993. PMID: 8246011

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