Takahashi T - Search Results

1

AMPK Complex Activation Promotes Sarcolemmal Repair in Dysferlinopathy.

Ono H, Suzuki N, Kanno SI, Kawahara G, Izumi R, Takahashi T, Kitajima Y, Osana S, Nakamura N, Akiyama T, Ikeda K, Shijo T, Mitsuzawa S, Nagatomi R, Araki N, Yasui A, Warita H, Hayashi YK, Miyake K, Aoki M. Ono H, et al. Among authors: takahashi t. Mol Ther. 2020 Apr 8;28(4):1133-1153. doi: 10.1016/j.ymthe.2020.02.006. Epub 2020 Feb 12. Mol Ther. 2020. PMID: 32087766 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

[A patient with limb girdle muscular dystrophy type 2B (LGMD2B) manifesting cardiomyopathy].

Kuru S, Yasuma F, Wakayama T, Kimura S, Konagaya M, Aoki M, Tanabe M, Takahashi T. Kuru S, et al. Among authors: takahashi t. Rinsho Shinkeigaku. 2004 Jun;44(6):375-8. Rinsho Shinkeigaku. 2004. PMID: 15293763 Japanese.

5

[A patient with distal muscular dystrophy without mutations in dysferlin gene but with abnormal dysferlin localization in muscle fibers].

Hozumi I, Takahashi T, Aoki M, Hayashi YK, Suzuki N, Matsuyama Z, Inuzuka T, Nonaka I. Hozumi I, et al. Among authors: takahashi t. Rinsho Shinkeigaku. 2004 Oct;44(10):699-702. Rinsho Shinkeigaku. 2004. PMID: 15568488 Japanese.

6

Dysferlinopathy associated with rigid spine syndrome.

Nagashima T, Chuma T, Mano Y, Goto Y, Hayashi YK, Minami N, Nishino I, Nonaka I, Takahashi T, Sawa H, Aoki M, Nagashima K. Nagashima T, et al. Among authors: takahashi t. Neuropathology. 2004 Dec;24(4):341-6. doi: 10.1111/j.1440-1789.2004.00573.x. Neuropathology. 2004. PMID: 15641596

7

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

8

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

9

[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.

10

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

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