Higuchi I - Search Results

1

Morphologic findings in biopsied skeletal muscle and cultured fibroblasts from a female patient with Danon's disease (lysosomal glycogen storage disease without acid maltase deficiency).

Usuki F, Takenaga S, Higuchi I, Kashio N, Nakagawa M, Osame M. Usuki F, et al. Among authors: higuchi i. J Neurol Sci. 1994 Dec 1;127(1):54-60. doi: 10.1016/0022-510x(94)90135-x. J Neurol Sci. 1994. PMID: 7699392

2

Muscular involvement in lysosomal acid lipase deficiency in rats.

Honda Y, Kuriyama M, Higuchi I, Fujiyama J, Yoshida H, Osame M. Honda Y, et al. Among authors: higuchi i. J Neurol Sci. 1992 Apr;108(2):189-95. doi: 10.1016/0022-510x(92)90050-u. J Neurol Sci. 1992. PMID: 1517751

3

Vacuolar myositis with expression of both MHC class I and class II antigens on skeletal muscle fibers.

Higuchi I, Nerenberg M, Ijichi T, Fukunaga H, Arimura K, Usuki F, Kuriyama M, Osame M. Higuchi I, et al. J Neurol Sci. 1991 Nov;106(1):60-6. doi: 10.1016/0022-510x(91)90195-d. J Neurol Sci. 1991. PMID: 1779240

4

Cardiomyopathy, mental retardation, and autophagic vacuolar myopathy. Abnormal MRI findings in the head.

Kashio N, Usuki F, Akamine T, Nakagawa S, Higuchi I, Nakahara K, Okada A, Osame M, Murata F. Kashio N, et al. Among authors: higuchi i. J Neurol Sci. 1991 Sep;105(1):1-5. doi: 10.1016/0022-510x(91)90109-k. J Neurol Sci. 1991. PMID: 1795162

5

Human acid maltase-deficient myogenic cell transformation with origin-defective SV40: characterization of a cloned line.

Usuki F, Higuchi I, Soejima Y, Hattori M, Maruyama I, Osame M. Usuki F, et al. Among authors: higuchi i. Muscle Nerve. 1991 Mar;14(3):245-52. doi: 10.1002/mus.880140308. Muscle Nerve. 1991. PMID: 2041545

6

Steroid-responsive myalgia in a patient with Becker muscular dystrophy.

Higuchi I, Nakamura K, Nakagawa M, Nakamura N, Usuki F, Inose M, Osame M. Higuchi I, et al. J Neurol Sci. 1993 Apr;115(2):219-22. doi: 10.1016/0022-510x(93)90228-q. J Neurol Sci. 1993. PMID: 7683333

7

Type II muscle fibers are stained by anti-Fas antibody.

Yamada H, Nakagawa M, Higuchi I, Ohkubo R, Osame M. Yamada H, et al. Among authors: higuchi i. J Neurol Sci. 1995 Dec;134(1-2):115-8. doi: 10.1016/0022-510x(95)00242-5. J Neurol Sci. 1995. PMID: 8747853

8

New missense mutation in the alpha-sarcoglycan gene in a Japanese patient with severe childhood autosomal recessive muscular dystrophy with incomplete alpha-sarcoglycan deficiency.

Higuchi I, Iwaki H, Kawai H, Endo T, Kunishige M, Fukunaga H, Nakagawa M, Arimura K, Osame M. Higuchi I, et al. J Neurol Sci. 1997 Dec 9;153(1):100-5. doi: 10.1016/s0022-510x(97)00182-2. J Neurol Sci. 1997. PMID: 9455986

9

Detection of DNA fragmentation of myonuclei in myotonic dystrophy by double staining with anti-emerin antibody and by nick end-labeling.

Yamada H, Nakagawa M, Higuchi I, Horikiri T, Osame M. Yamada H, et al. Among authors: higuchi i. J Neurol Sci. 2000 Feb 15;173(2):97-102. doi: 10.1016/s0022-510x(99)00306-8. J Neurol Sci. 2000. PMID: 10675651

10

Autosomal dominant early onset dementia and leukoencephalopathy in a Japanese family: clinical, neuroimaging and genetic studies.

Utatsu Y, Takashima H, Michizono K, Kanda N, Endou K, Mitsuyama Y, Fujimoto T, Nagai M, Umehara F, Higuchi I, Arimura K, Nakagawa M, Osame M. Utatsu Y, et al. Among authors: higuchi i. J Neurol Sci. 1997 Mar 20;147(1):55-62. doi: 10.1016/s0022-510x(96)05310-5. J Neurol Sci. 1997. PMID: 9094061

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