Osame M - Search Results

1

Hereditary Motor and Sensory Neuropathy with Proximal Dominant Involvement: Clinical, Pathological, and Genetic Features.

Nakagawa M, Takashima H, Suehara M, Saito M, Saito A, Kanzato N, Matsuzaki T, Hirata K, Izumo S, Terwilliger JD, Osame M. Nakagawa M, et al. Among authors: osame m. Ann N Y Acad Sci. 1999 Oct;883(1):449-452. doi: 10.1111/j.1749-6632.1999.tb08607.x. Ann N Y Acad Sci. 1999. PMID: 29086967 No abstract available.

2

Autosomal dominant palatal myoclonus and spinal cord atrophy.

Okamoto Y, Mitsuyama H, Jonosono M, Hirata K, Arimura K, Osame M, Nakagawa M. Okamoto Y, et al. Among authors: osame m. J Neurol Sci. 2002 Mar 15;195(1):71-6. doi: 10.1016/s0022-510x(01)00687-6. J Neurol Sci. 2002. PMID: 11867077

3

Altered trafficking and adhesion function of MPZ mutations and phenotypes of Charcot-Marie-Tooth disease 1B.

Matsuyama W, Nakagawa M, Takashima H, Osame M. Matsuyama W, et al. Among authors: osame m. Acta Neuropathol. 2002 May;103(5):501-8. doi: 10.1007/s00401-001-0497-1. Epub 2002 Jan 31. Acta Neuropathol. 2002. PMID: 11935267

4

A prospective uncontrolled trial of fermented milk drink containing viable Lactobacillus casei strain Shirota in the treatment of HTLV-1 associated myelopathy/tropical spastic paraparesis.

Matsuzaki T, Saito M, Usuku K, Nose H, Izumo S, Arimura K, Osame M. Matsuzaki T, et al. Among authors: osame m. J Neurol Sci. 2005 Oct 15;237(1-2):75-81. doi: 10.1016/j.jns.2005.05.011. J Neurol Sci. 2005. PMID: 15961107 Clinical Trial.

5

Miyoshi myopathy patients with novel 5' splicing donor site mutations showed different dysferlin immunostaining at the sarcolemma.

Saito A, Higuchi I, Nakagawa M, Saito M, Hirata K, Suehara M, Yoshida Y, Takahashi T, Aoki M, Osame M. Saito A, et al. Among authors: osame m. Acta Neuropathol. 2002 Dec;104(6):615-20. doi: 10.1007/s00401-002-0593-x. Epub 2002 Jul 19. Acta Neuropathol. 2002. PMID: 12410383 Review.

6

Molecular mechanism of rigid spine with muscular dystrophy type 1 caused by novel mutations of selenoprotein N gene.

Okamoto Y, Takashima H, Higuchi I, Matsuyama W, Suehara M, Nishihira Y, Hashiguchi A, Hirano R, Ng AR, Nakagawa M, Izumo S, Osame M, Arimura K. Okamoto Y, et al. Among authors: osame m. Neurogenetics. 2006 Jul;7(3):175-83. doi: 10.1007/s10048-006-0046-0. Epub 2006 Jun 15. Neurogenetics. 2006. PMID: 16779558

7

Pathological characteristics of skeletal muscle in Ullrich's disease with collagen VI deficiency.

Higuchi I, Horikiri T, Niiyama T, Suehara M, Shiraishi T, Hu J, Uchida Y, Saito A, Nakagawa M, Arimura K, Osame M. Higuchi I, et al. Among authors: osame m. Neuromuscul Disord. 2003 May;13(4):310-6. doi: 10.1016/s0960-8966(02)00282-1. Neuromuscul Disord. 2003. PMID: 12868500

8

Electron microscopic abnormalities of skeletal muscle in patients with collagen VI deficiency in Ullrich's disease.

Niiyama T, Higuchi I, Suehara M, Hashiguchi T, Shiraishi T, Nakagawa M, Arimura K, Maruyama I, Osame M. Niiyama T, et al. Among authors: osame m. Acta Neuropathol. 2002 Jul;104(1):67-71. doi: 10.1007/s00401-002-0522-z. Epub 2002 Apr 30. Acta Neuropathol. 2002. PMID: 12070666

9

Molecular analysis of T cell clonotypes in muscle-infiltrating lymphocytes from patients with human T lymphotropic virus type 1 polymyositis.

Saito M, Higuchi I, Saito A, Izumo S, Usuku K, Bangham CR, Osame M. Saito M, et al. Among authors: osame m. J Infect Dis. 2002 Nov 1;186(9):1231-41. doi: 10.1086/344315. Epub 2002 Oct 7. J Infect Dis. 2002. PMID: 12402192

10

Fibronectin receptor reduction in skin and fibroblasts of patients with Ullrich's disease.

Hu J, Higuchi I, Shiraishi T, Suehara M, Niiyama T, Horikiri T, Uchida Y, Saito A, Osame M. Hu J, et al. Among authors: osame m. Muscle Nerve. 2002 Nov;26(5):696-701. doi: 10.1002/mus.10250. Muscle Nerve. 2002. PMID: 12402292

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