Osame M - Search Results

1

Myoadenylate deaminase deficiency with progressive muscle weakness and atrophy caused by new missense mutations in AMPD1 gene: case report in a Japanese patient.

Abe M, Higuchi I, Morisaki H, Morisaki T, Osame M. Abe M, et al. Among authors: osame m. Neuromuscul Disord. 2000 Oct;10(7):472-7. doi: 10.1016/s0960-8966(00)00127-9. Neuromuscul Disord. 2000. PMID: 10996775

2

Abnormal expression of heparin sulfate proteoglycan on basal lamina of muscle fibers in two Japanese patients with adhalin deficiency.

Higuchi I, Fukunaga H, Matsumura K, Inose M, Izumi K, Okubo R, Nakagawa M, Shimizu T, Osame M. Higuchi I, et al. Among authors: osame m. Neuromuscul Disord. 1995 Nov;5(6):467-74. doi: 10.1016/0960-8966(95)00010-k. Neuromuscul Disord. 1995. PMID: 8580728

3

First missense mutations (R388W and R425H) of AMPD1 accompanied with myopathy found in a Japanese patient.

Morisaki H, Higuchi I, Abe M, Osame M, Morisaki T. Morisaki H, et al. Among authors: osame m. Hum Mutat. 2000 Dec;16(6):467-72. doi: 10.1002/1098-1004(200012)16:6<467::AID-HUMU3>3.0.CO;2-V. Hum Mutat. 2000. PMID: 11102975

4

Familial facioscapulohumeral muscular dystrophy: phenotypic diversity and genetic abnormality.

Nakagawa M, Higuchi I, Yoshidome H, Isashiki Y, Ohkubo R, Kaseda S, Iwaki H, Fukunaga H, Osame M. Nakagawa M, et al. Among authors: osame m. Acta Neurol Scand. 1996 Feb-Mar;93(2-3):189-92. doi: 10.1111/j.1600-0404.1996.tb00197.x. Acta Neurol Scand. 1996. PMID: 8741141

5

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. Among authors: osame m. J Neurol Sci. 1997 Dec 9;153(1):100-5. doi: 10.1016/s0022-510x(97)00182-2. J Neurol Sci. 1997. PMID: 9455986

6

Familial skeletal myopathy with atrioventricular block.

Ohkubo R, Nakagawa M, Higuchi I, Utatsu Y, Miyazato H, Atsuchi Y, Osame M. Ohkubo R, et al. Among authors: osame m. Intern Med. 1999 Nov;38(11):856-60. doi: 10.2169/internalmedicine.38.856. Intern Med. 1999. PMID: 10563745 Free article.

7

[A study of clinical symptoms, muscle pathology, therapeutic response, and prognosis of myositis in patients with HTLV-1 associated myelopathy (HAM)].

Inose M, Higuchi I, Yoshimine K, Arimura K, Osame M, Izumo S, Hokezu Y. Inose M, et al. Among authors: osame m. Rinsho Shinkeigaku. 1999 Aug;39(8):807-11. Rinsho Shinkeigaku. 1999. PMID: 10586623 Clinical Trial. Japanese.

8

Mitochondrial myopathy and familial thiamine deficiency.

Sato Y, Nakagawa M, Higuchi I, Osame M, Naito E, Oizumi K. Sato Y, et al. Among authors: osame m. Muscle Nerve. 2000 Jul;23(7):1069-75. doi: 10.1002/1097-4598(200007)23:7<1069::aid-mus9>3.0.co;2-0. Muscle Nerve. 2000. PMID: 10883001

9

Microvascular endothelial abnormality in skeletal muscle from a patient with gastric cancer without dermatomyositis.

Higuchi I, Niiyama T, Uchida Y, Inose M, Hu J, Nakagawa M, Arimura K, Osame M. Higuchi I, et al. Among authors: osame m. Acta Neuropathol. 2000 Dec;100(6):718-22. doi: 10.1007/s004010000243. Acta Neuropathol. 2000. PMID: 11078226

10

Phenotypic variation in a large Japanese family with Miyoshi myopathy with nonsense mutation in exon 19 of dysferlin gene.

Nakagawa M, Matsuzaki T, Suehara M, Kanzato N, Takashima H, Higuchi I, Matsumura T, Goto K, Arahata K, Osame M. Nakagawa M, et al. Among authors: osame m. J Neurol Sci. 2001 Feb 15;184(1):15-9. doi: 10.1016/s0022-510x(00)00484-6. J Neurol Sci. 2001. PMID: 11231027

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