Takahashi T - Search Results

1

Multicenter questionnaire survey for sporadic inclusion body myositis in Japan.

Suzuki N, Mori-Yoshimura M, Yamashita S, Nakano S, Murata KY, Inamori Y, Matsui N, Kimura E, Kusaka H, Kondo T, Higuchi I, Kaji R, Tateyama M, Izumi R, Ono H, Kato M, Warita H, Takahashi T, Nishino I, Aoki M. Suzuki N, et al. Among authors: takahashi t. Orphanet J Rare Dis. 2016 Nov 8;11(1):146. doi: 10.1186/s13023-016-0524-x. Orphanet J Rare Dis. 2016. PMID: 27821140 Free PMC article.

2

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: takahashi t. 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.

3

Novel dysferlin mutations and characteristic muscle atrophy in late-onset Miyoshi myopathy.

Suzuki N, Aoki M, Takahashi T, Takano D, Asano M, Shiga Y, Onodera Y, Tateyama M, Itoyama Y. Suzuki N, et al. Among authors: takahashi t. Muscle Nerve. 2004 May;29(5):721-3. doi: 10.1002/mus.20025. Muscle Nerve. 2004. PMID: 15116377

4

Expression profiling with progression of dystrophic change in dysferlin-deficient mice (SJL).

Suzuki N, Aoki M, Hinuma Y, Takahashi T, Onodera Y, Ishigaki A, Kato M, Warita H, Tateyama M, Itoyama Y. Suzuki N, et al. Among authors: takahashi t. Neurosci Res. 2005 May;52(1):47-60. doi: 10.1016/j.neures.2005.01.006. Neurosci Res. 2005. PMID: 15811552

5

Late-onset distal myopathy with rimmed vacuoles without mutation in the GNE or dysferlin genes.

Suzuki N, Aoki M, Mizuno H, Onodera Y, Takahashi T, Nagata T, Tateyama M, Itoyama Y. Suzuki N, et al. Among authors: takahashi t. Muscle Nerve. 2005 Dec;32(6):812-4. doi: 10.1002/mus.20417. Muscle Nerve. 2005. PMID: 16116644

6

[Mutational and clinical features of Japanese patients with dysferlinopathy (Miyoshi myopathy and limb girdle muscular dystrophy type 2B)].

Aoki M, Takahashi T. Aoki M, et al. Among authors: takahashi t. Rinsho Shinkeigaku. 2005 Nov;45(11):938-42. Rinsho Shinkeigaku. 2005. PMID: 16447768 Review. Japanese.

7

A case of dysferlinopathy presenting choreic movements.

Takahashi T, Aoki M, Imai T, Yoshioka M, Konno H, Higano S, Onodera Y, Saito H, Kimura I, Itoyama Y. Takahashi T, et al. Mov Disord. 2006 Sep;21(9):1513-5. doi: 10.1002/mds.21027. Mov Disord. 2006. PMID: 16817213

8

Distal anterior compartment myopathy with early ankle contractures.

Saito H, Suzuki N, Ishiguro H, Hirota K, Itoyama Y, Takahashi T, Aoki M. Saito H, et al. Among authors: takahashi t. Muscle Nerve. 2007 Oct;36(4):525-7. doi: 10.1002/mus.20836. Muscle Nerve. 2007. PMID: 17614318

9

Rapid screening for Japanese dysferlinopathy by fluorescent primer extension.

Hayashi S, Ohsawa Y, Takahashi T, Suzuki N, Okada T, Rikimaru M, Murakami T, Aoki M, Sunada Y. Hayashi S, et al. Among authors: takahashi t. Intern Med. 2010;49(24):2693-6. doi: 10.2169/internalmedicine.49.3771. Epub 2010 Dec 15. Intern Med. 2010. PMID: 21173544 Free article.

10

Continuous administration of poloxamer 188 reduces overload-induced muscular atrophy in dysferlin-deficient SJL mice.

Suzuki N, Akiyama T, Takahashi T, Komuro H, Warita H, Tateyama M, Itoyama Y, Aoki M. Suzuki N, et al. Among authors: takahashi t. Neurosci Res. 2012 Feb;72(2):181-6. doi: 10.1016/j.neures.2011.10.005. Epub 2011 Oct 21. Neurosci Res. 2012. PMID: 22044584 Free article.

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