Takahashi Y - Search Results

1

Distinctive chaperonopathy in skeletal muscle associated with the dominant variant in DNAJB4.

Inoue M, Noguchi S, Inoue YU, Iida A, Ogawa M, Bengoechea R, Pittman SK, Hayashi S, Watanabe K, Hosoi Y, Sano T, Takao M, Oya Y, Takahashi Y, Miyajima H, Weihl CC, Inoue T, Nishino I. Inoue M, et al. Among authors: takahashi y. Acta Neuropathol. 2023 Feb;145(2):235-255. doi: 10.1007/s00401-022-02530-4. Epub 2022 Dec 13. Acta Neuropathol. 2023. PMID: 36512060

2

[A case of chronic sarcoid myopathy with Basedow's disease and Sjogren's syndrome: A case series of sarcoid myopathy].

Isobe T, Mori-Yoshimura M, Oya Y, Saito Y, Murata M, Nishino I, Takahashi Y. Isobe T, et al. Among authors: takahashi y. Rinsho Shinkeigaku. 2017 May 27;57(5):220-224. doi: 10.5692/clinicalneurol.cn-001012. Epub 2017 Apr 27. Rinsho Shinkeigaku. 2017. PMID: 28450690 Japanese.

3

[Childhood-onset anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (anti-HMGCR) necrotizing myopathy needs to be distinguished from muscular dystrophy: A case study].

Hama Y, Mori-Yoshimura M, Komaki H, Suzuki S, Kohsaka H, Nishino I, Takahashi Y. Hama Y, et al. Among authors: takahashi y. Rinsho Shinkeigaku. 2017 Oct 27;57(10):567-572. doi: 10.5692/clinicalneurol.cn-001040. Epub 2017 Sep 30. Rinsho Shinkeigaku. 2017. PMID: 28966227 Japanese.

4

Cardiac conduction disturbances and aging in patients with Duchenne muscular dystrophy.

Segawa K, Komaki H, Mori-Yoshimura M, Oya Y, Kimura K, Tachimori H, Kato N, Sasaki M, Takahashi Y. Segawa K, et al. Among authors: takahashi y. Medicine (Baltimore). 2017 Oct;96(42):e8335. doi: 10.1097/MD.0000000000008335. Medicine (Baltimore). 2017. PMID: 29049249 Free PMC article.

5

[Two cases of nemaline myopathy presenting with hypertrophy of distal limbs with prominent asymmetry].

Mizuno Y, Mori-Yoshimura M, Oya Y, Nishikawa A, Nishino I, Takahashi Y. Mizuno Y, et al. Among authors: takahashi y. Rinsho Shinkeigaku. 2017 Nov 25;57(11):691-697. doi: 10.5692/clinicalneurol.cn-001024. Epub 2017 Oct 26. Rinsho Shinkeigaku. 2017. PMID: 29070751 Japanese.

6

Social involvement issues in patients with Becker muscular dystrophy: A questionnaire survey of subjects from a patient registry.

Mori-Yoshimura M, Mizuno Y, Yoshida S, Minami N, Yonemoto N, Takeuchi F, Nishino I, Murata M, Takeda S, Takahashi Y, Kimura E. Mori-Yoshimura M, et al. Among authors: takahashi y. Brain Dev. 2018 Apr;40(4):268-277. doi: 10.1016/j.braindev.2017.11.004. Epub 2017 Nov 29. Brain Dev. 2018. PMID: 29196072

7

Characteristics of Japanese Patients with Becker Muscular Dystrophy and Intermediate Muscular Dystrophy in a Japanese National Registry of Muscular Dystrophy (Remudy): Heterogeneity and Clinical Variation.

Mori-Yoshimura M, Mitsuhashi S, Nakamura H, Komaki H, Goto K, Yonemoto N, Takeuchi F, Hayashi YK, Murata M, Takahashi Y, Nishino I, Takeda S, Kimura E. Mori-Yoshimura M, et al. Among authors: takahashi y. J Neuromuscul Dis. 2018;5(2):193-203. doi: 10.3233/JND-170225. J Neuromuscul Dis. 2018. PMID: 29614690 Free PMC article.

8

Two novel VCP missense variants identified in Japanese patients with multisystem proteinopathy.

Inoue M, Iida A, Hayashi S, Mori-Yoshimura M, Nagaoka A, Yoshimura S, Shiraishi H, Tsujino A, Takahashi Y, Nonaka I, Hayashi YK, Noguchi S, Nishino I. Inoue M, et al. Among authors: takahashi y. Hum Genome Var. 2018 May 30;5:9. doi: 10.1038/s41439-018-0009-7. eCollection 2018. Hum Genome Var. 2018. PMID: 29899994 Free PMC article.

9

Emery-Dreifuss muscular dystrophy-related myopathy with TMEM43 mutations.

Mukai T, Mori-Yoshimura M, Nishikawa A, Hokkoku K, Sonoo M, Nishino I, Takahashi Y. Mukai T, et al. Among authors: takahashi y. Muscle Nerve. 2019 Feb;59(2):E5-E7. doi: 10.1002/mus.26355. Epub 2018 Nov 13. Muscle Nerve. 2019. PMID: 30311943 No abstract available.

10

Phenotype of a limb-girdle congenital myasthenic syndrome patient carrying a GFPT1 mutation.

Matsumoto C, Mori-Yoshimura M, Noguchi S, Endo Y, Oya Y, Murata M, Nishino I, Takahashi Y. Matsumoto C, et al. Among authors: takahashi y. Brain Dev. 2019 May;41(5):470-473. doi: 10.1016/j.braindev.2018.12.002. Epub 2019 Mar 4. Brain Dev. 2019. PMID: 30846217

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