Matsumura T - Search Results

1

Protein and gene analyses of dysferlinopathy in a large group of Japanese muscular dystrophy patients.

Tagawa K, Ogawa M, Kawabe K, Yamanaka G, Matsumura T, Goto K, Nonaka I, Nishino I, Hayashi YK. Tagawa K, et al. Among authors: matsumura t. J Neurol Sci. 2003 Jul 15;211(1-2):23-8. doi: 10.1016/s0022-510x(03)00041-8. J Neurol Sci. 2003. PMID: 12767493

2

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: matsumura t. J Neurol Sci. 2001 Feb 15;184(1):15-9. doi: 10.1016/s0022-510x(00)00484-6. J Neurol Sci. 2001. PMID: 11231027

3

Tongue atrophy in facioscapulohumeral muscular dystrophy.

Yamanaka G, Goto K, Matsumura T, Funakoshi M, Komori T, Hayashi YK, Arahata K. Yamanaka G, et al. Among authors: matsumura t. Neurology. 2001 Aug 28;57(4):733-5. doi: 10.1212/wnl.57.4.733. Neurology. 2001. PMID: 11524495

4

Chromosome 4q;10q translocations; comparison with different ethnic populations and FSHD patients.

Matsumura T, Goto K, Yamanaka G, Lee JH, Zhang C, Hayashi YK, Arahata K. Matsumura T, et al. BMC Neurol. 2002 Aug 20;2:7. doi: 10.1186/1471-2377-2-7. BMC Neurol. 2002. PMID: 12188928 Free PMC article.

5

[An ambiguous pedigree of facioscapulohumeral muscular dystrophy which showed double EcoRI/BlnI resistant short fragments].

Matsumura T, Etoh M, Goto K, Saito T, Nozaki S, Fujimura H, Shinno S. Matsumura T, et al. Rinsho Shinkeigaku. 2002 Apr;42(4):313-6. Rinsho Shinkeigaku. 2002. PMID: 12561087 Japanese.

6

Dysferlin mutations in Japanese Miyoshi myopathy: relationship to phenotype.

Takahashi T, Aoki M, Tateyama M, Kondo E, Mizuno T, Onodera Y, Takano R, Kawai H, Kamakura K, Mochizuki H, Shizuka-Ikeda M, Nakagawa M, Yoshida Y, Akanuma J, Hoshino K, Saito H, Nishizawa M, Kato S, Saito K, Miyachi T, Yamashita H, Kawai M, Matsumura T, Kuzuhara S, Ibi T, Sahashi K, Nakai H, Kohnosu T, Nonaka I, Arahata K, Brown RH Jr, Saito H, Itoyama Y. Takahashi T, et al. Among authors: matsumura t. Neurology. 2003 Jun 10;60(11):1799-804. doi: 10.1212/01.wnl.0000068333.43005.12. Neurology. 2003. PMID: 12796534

7

Necklace cytoplasmic bodies in hereditary myopathy with early respiratory failure.

Uruha A, Hayashi YK, Oya Y, Mori-Yoshimura M, Kanai M, Murata M, Kawamura M, Ogata K, Matsumura T, Suzuki S, Takahashi Y, Kondo T, Kawarabayashi T, Ishii Y, Kokubun N, Yokoi S, Yasuda R, Kira J, Mitsuhashi S, Noguchi S, Nonaka I, Nishino I. Uruha A, et al. Among authors: matsumura t. J Neurol Neurosurg Psychiatry. 2015 May;86(5):483-9. doi: 10.1136/jnnp-2014-309009. Epub 2014 Sep 24. J Neurol Neurosurg Psychiatry. 2015. PMID: 25253871

8

Renal dysfunction can be a common complication in patients with myotonic dystrophy 1.

Matsumura T, Saito T, Yonemoto N, Nakamori M, Sugiura T, Nakamori A, Fujimura H, Sakoda S. Matsumura T, et al. J Neurol Sci. 2016 Sep 15;368:266-71. doi: 10.1016/j.jns.2016.07.036. Epub 2016 Jul 15. J Neurol Sci. 2016. PMID: 27538647

9

Metabolic complications in myotonic dystrophy type 1: A cross-sectional survey using the National Registry of Japan.

Hama M, Horie R, Kubota T, Matsumura T, Kimura E, Nakamura H, Takahashi MP, Takada H. Hama M, et al. Among authors: matsumura t. J Neurol Sci. 2021 Aug 15;427:117511. doi: 10.1016/j.jns.2021.117511. Epub 2021 May 27. J Neurol Sci. 2021. PMID: 34082146

10

Clinical trajectory of a patient with filaminopathy who developed arrhythmogenic cardiomyopathy, myofibrillar myopathy, and multiorgan tumors.

Matsumura T, Inoue K, Toyooka K, Inoue M, Iida A, Saito Y, Nishikawa T, Moriuchi K, Beck G, Nishino I, Fujimura H. Matsumura T, et al. Neuromuscul Disord. 2021 Dec;31(12):1282-1286. doi: 10.1016/j.nmd.2021.10.002. Epub 2021 Oct 9. Neuromuscul Disord. 2021. PMID: 34857437

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