Shishikura K - Search Results

1

Ependymal abnormalities in lissencephaly/pachygyria.

Sarnat HB, Darwish HZ, Barth PG, Trevenen CL, Pinto A, Kotagal S, Shishikura K, Osawa M, Korobkin R. Sarnat HB, et al. Among authors: shishikura k. J Neuropathol Exp Neurol. 1993 Sep;52(5):525-41. doi: 10.1097/00005072-199309000-00011. J Neuropathol Exp Neurol. 1993. PMID: 8360705

2

Fukuyama type congenital progressive muscular dystrophy.

Osawa M, Arai Y, Ikenaka H, Murasugi H, Sugahara N, Sumida S, Okada N, Shishikura K, Suzuki H, Hirayama Y, et al. Osawa M, et al. Among authors: shishikura k. Acta Paediatr Jpn. 1991 Apr;33(2):261-9. doi: 10.1111/j.1442-200x.1991.tb01552.x. Acta Paediatr Jpn. 1991. PMID: 1957653 Review.

3

[Progressive bulbar paralysis in childhood (Fazio-Londe disease)].

Shishikura K, Osawa M. Shishikura K, et al. Ryoikibetsu Shokogun Shirizu. 1999;(27 Pt 2):339-42. Ryoikibetsu Shokogun Shirizu. 1999. PMID: 10434668 Review. Japanese. No abstract available.

4

Clinical variability of congenital myopathy with type 1 fiber atrophy: a long-term observation of three cases.

Shishikura K, Osawa M, Suzuki H, Hirayama Y, Arai Y, Sumida S, Takahashi R, Fukuyama Y. Shishikura K, et al. Acta Paediatr Jpn. 1994 Apr;36(2):186-93. doi: 10.1111/j.1442-200x.1994.tb03159.x. Acta Paediatr Jpn. 1994. PMID: 8203265

5

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: shishikura k. Brain Dev. 1987;9(1):61-4. doi: 10.1016/s0387-7604(87)80013-x. Brain Dev. 1987. PMID: 3605541

6

Computed tomography and magnetic resonance imaging of affected muscle in childhood acid alpha-glucosidase deficiency: a case report.

Arai Y, Osawa M, Shishikura K, Suzuki H, Saito K, Fukuyama Y, Sugie H. Arai Y, et al. Among authors: shishikura k. Brain Dev. 1993 Mar-Apr;15(2):147-52. doi: 10.1016/0387-7604(93)90053-b. Brain Dev. 1993. PMID: 8214335

7

[Spinal muscular atrophy (type I, II)].

Saito K, Shishikura K, Suzuki H, Osawa M. Saito K, et al. Among authors: shishikura k. Ryoikibetsu Shokogun Shirizu. 1999;(27 Pt 2):364-70. Ryoikibetsu Shokogun Shirizu. 1999. PMID: 10434675 Review. Japanese. No abstract available.

8

[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: shishikura k. No To Hattatsu. 1990 Jan;22(1):55-60. No To Hattatsu. 1990. PMID: 2403811 Japanese.

9

[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: shishikura k. No To Hattatsu. 1989 Jul;21(4):361-8. No To Hattatsu. 1989. PMID: 2675944 Japanese.

10

[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. Among authors: shishikura k. No To Hattatsu. 1983 Jul;15(4):290-300. No To Hattatsu. 1983. PMID: 6412732 Japanese. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

60 results

Search Page