Suzuki H - Search Results

1

[Genetic studies of Duchenne muscular dystrophy families using the dystrophy families using the dystrophin cDNA].

Saito K, Tanaka A, Harada T, Ikeya K, Fukuyama Y, Arahata K, Sugita H, Osawa M, Shishikura K, Suzuki H. Saito K, et al. Among authors: suzuki h. No To Hattatsu. 1989 Jul;21(4):361-8. No To Hattatsu. 1989. PMID: 2675944 Japanese.

2

[Skeletal muscle CT scan and ultrasound imaging in two siblings with central core disease].

Arai Y, Sumida S, Osawa M, Hirasawa K, Okada N, Kawai M, Shishikura K, Suzuki H, Hirayama Y, Saito K, et al. Arai Y, et al. Among authors: suzuki h. No To Hattatsu. 1990 Jan;22(1):55-60. No To Hattatsu. 1990. PMID: 2403811 Japanese.

3

[A histological study of mitochondrial myopathy in partial deficiency of pyruvate dehydrogenase complex].

Suzuki H, Shishikura K, Osawa M, Hirayama Y, Motegi R, Mitsuishi Y, Yamaguchi K, Fukuyama Y. Suzuki H, et al. No To Hattatsu. 1983 Jul;15(4):290-300. No To Hattatsu. 1983. PMID: 6412732 Japanese. No abstract available.

4

Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations.

Fukuyama Y, Osawa M, Suzuki H. Fukuyama Y, et al. Among authors: suzuki h. Brain Dev. 1981;3(1):1-29. doi: 10.1016/s0387-7604(81)80002-2. Brain Dev. 1981. PMID: 7258547

5

Improvement of action myoclonus by an administration of 5-hydroxytryptophan and carbidopa in a child with muscular subsarcolemmal hyperactivity.

Nakano K, Hayakawa T, Shishikura K, Ohsawa M, Suzuki H, Fukuyama Y. Nakano K, et al. Among authors: suzuki h. Brain Dev. 1990;12(5):516-20. doi: 10.1016/s0387-7604(12)80218-x. Brain Dev. 1990. PMID: 2288384

6

[Home-stay respiratory management of a child with nemaline myopathy by using a negative pressure-controlled respirator].

Ikeya K, Kajiyama M, Hirasawa K, Ohsawa M, Shishikura K, Suzuki H, Fukuyama Y. Ikeya K, et al. Among authors: suzuki h. No To Hattatsu. 1988;20(5):423-8. No To Hattatsu. 1988. PMID: 3224016 Japanese. No abstract available.

7

Nonspecific congenital myopathy (minimal change myopathy): a case report.

Jong YJ, Shishikura K, Aoyama M, Kitahara H, Horita H, Osawa M, Suzuki H, Hirayama Y, Nakada E, Saito K, et al. Jong YJ, et al. Among authors: suzuki h. Brain Dev. 1987;9(1):61-4. doi: 10.1016/s0387-7604(87)80013-x. Brain Dev. 1987. PMID: 3605541

8

[Hypothalamic GH Deficiency and gelastic seizures in a 10-year-old girl with MELAS].

Matsuzaki M, Izumi T, Ebato K, Suzuki H, Shishikura K, Osawa M, Fukuyama Y, Shimizu N. Matsuzaki M, et al. Among authors: suzuki h. No To Hattatsu. 1991 Jul;23(4):411-6. No To Hattatsu. 1991. PMID: 1873057 Japanese.

9

[Dramatic effects of high-dose intravenous gammaglobulin in each patient with intractable dermatomyositis and polymyositis].

Morita R, Nakano K, Hirano Y, Izumi T, Hirayama Y, Suzuki H, Shishikura K, Okada N, Osawa M, Fukuyama Y. Morita R, et al. Among authors: suzuki h. No To Hattatsu. 1989 Nov;21(6):523-8. No To Hattatsu. 1989. PMID: 2478176 Japanese.

10

[Sequential muscle biopsy in Lafora type myoclonus epilepsy].

Shishikura K, Umezu R, Aoyama M, Hirayama Y, Suzuki H, Osawa M, Fukuyama Y, Kamoshita S, Hara M. Shishikura K, et al. Among authors: suzuki h. No To Hattatsu. 1983 Nov;15(6):467-77. No To Hattatsu. 1983. PMID: 6416274 Japanese. No abstract available.

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