Nonaka I - Search Results

1

Autophagic vacuoles with sarcolemmal features delineate Danon disease and related myopathies.

Sugie K, Noguchi S, Kozuka Y, Arikawa-Hirasawa E, Tanaka M, Yan C, Saftig P, von Figura K, Hirano M, Ueno S, Nonaka I, Nishino I. Sugie K, et al. Among authors: nonaka i. J Neuropathol Exp Neurol. 2005 Jun;64(6):513-22. doi: 10.1093/jnen/64.6.513. J Neuropathol Exp Neurol. 2005. PMID: 15977643

2

Progressive cytochrome c oxidase deficiency in a case of Leigh's encephalomyelopathy.

Koga Y, Nonaka I, Nakao M, Yoshino M, Tanaka M, Ozawa T, Nakase H, DiMauro S. Koga Y, et al. Among authors: nonaka i. J Neurol Sci. 1990 Jan;95(1):63-76. doi: 10.1016/0022-510x(90)90117-6. J Neurol Sci. 1990. PMID: 2159985

3

Nemaline myopathy: comparative muscle histochemistry in the severe neonatal, moderate congenital, and adult-onset forms.

Shimomura C, Nonaka I. Shimomura C, et al. Among authors: nonaka i. Pediatr Neurol. 1989 Jan-Feb;5(1):25-31. doi: 10.1016/0887-8994(89)90005-2. Pediatr Neurol. 1989. PMID: 2712935

4

Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency.

Koga Y, Nonaka I, Kobayashi M, Tojyo M, Nihei K. Koga Y, et al. Among authors: nonaka i. Ann Neurol. 1988 Dec;24(6):749-56. doi: 10.1002/ana.410240609. Ann Neurol. 1988. PMID: 3144939

5

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

6

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: nonaka i. Neuromuscul Disord. 1995 Sep;5(5):429-38. doi: 10.1016/0960-8966(94)00087-p. Neuromuscul Disord. 1995. PMID: 7496177

7

Sarcolemmal indentation in cardiomyopathy with mental retardation and vacuolar myopathy.

Murakami N, Goto Y, Itoh M, Katsumi Y, Wada T, Ozawa E, Nonaka I. Murakami N, et al. Among authors: nonaka i. Neuromuscul Disord. 1995 Mar;5(2):149-55. doi: 10.1016/0960-8966(94)00046-c. Neuromuscul Disord. 1995. PMID: 7539316

8

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.

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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