Saito Y - Search Results

1

[A Japanese family with POMT2-related limb girdle muscular dystrophy].

Tomita Y, Matusya N, Narita T, Saito Y, Nishino I, Fukudome T. Tomita Y, et al. Among authors: saito y. Rinsho Shinkeigaku. 2021 Jun 29;61(6):378-384. doi: 10.5692/clinicalneurol.cn-001547. Epub 2021 May 20. Rinsho Shinkeigaku. 2021. PMID: 34011809 Japanese.

2

[A case of Emery-Dreifuss muscular dystrophy with slight joint contracture].

Fujii S, Eguchi K, Sato C, Saito Y, Indrawati LA, Shirai S, Nishino I, Yabe I. Fujii S, et al. Among authors: saito y. Rinsho Shinkeigaku. 2020 Aug 7;60(8):554-559. doi: 10.5692/clinicalneurol.60.cn-001431. Epub 2020 Jul 7. Rinsho Shinkeigaku. 2020. PMID: 32641626 Japanese.

3

[Clinicopathological Features of Myositis and Necrotizing Myopathy: How to Distinguish between Myositis and Muscular Dystrophy on Muscle Pathology].

Saito Y, Nishino I. Saito Y, et al. Brain Nerve. 2021 Feb;73(2):147-159. doi: 10.11477/mf.1416201727. Brain Nerve. 2021. PMID: 33561829 Japanese.

4

Causative variant profile of collagen VI-related dystrophy in Japan.

Inoue M, Saito Y, Yonekawa T, Ogawa M, Iida A, Nishino I, Noguchi S. Inoue M, et al. Among authors: saito y. Orphanet J Rare Dis. 2021 Jun 24;16(1):284. doi: 10.1186/s13023-021-01921-2. Orphanet J Rare Dis. 2021. PMID: 34167565 Free PMC article.

5

FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients.

Awano H, Saito Y, Shimizu M, Sekiguchi K, Niijima S, Matsuo M, Maegaki Y, Izumi I, Kikuchi C, Ishibashi M, Okazaki T, Komaki H, Iijima K, Nishino I. Awano H, et al. Among authors: saito y. J Clin Neurosci. 2021 Oct;92:215-221. doi: 10.1016/j.jocn.2021.08.014. Epub 2021 Aug 28. J Clin Neurosci. 2021. PMID: 34509255

6

Determining neurodevelopmental manifestations in Duchenne muscular dystrophy using a battery of brief tests.

Saito Y, Takeshita E, Komaki H, Nishino I, Sasaki M. Saito Y, et al. J Neurol Sci. 2022 Sep 15;440:120340. doi: 10.1016/j.jns.2022.120340. Epub 2022 Jul 13. J Neurol Sci. 2022. PMID: 35849899

7

Identification of a novel mutation and genotype-phenotype relationship in MEGF10 myopathy.

Fujii K, Hirano M, Terayama A, Inada R, Saito Y, Nishino I, Nagai Y. Fujii K, et al. Among authors: saito y. Neuromuscul Disord. 2022 May;32(5):436-440. doi: 10.1016/j.nmd.2022.01.009. Epub 2022 Jan 31. Neuromuscul Disord. 2022. PMID: 35370044

8

A 78-year-old Japanese male with late-onset PHKA1-associated distal myopathy: Case report and literature review.

Mori-Yoshimura M, Aizawa K, Oya Y, Saito Y, Fukuda T, Sugie H, Nishino I, Takahashi Y. Mori-Yoshimura M, et al. Among authors: saito y. Neuromuscul Disord. 2022 Sep;32(9):769-773. doi: 10.1016/j.nmd.2022.05.010. Epub 2022 May 24. Neuromuscul Disord. 2022. PMID: 35710611 Review.

9

Maximal Multistage Shuttle Run Test-induced Myalgia in a Patient with Muscle Phosphorylase B Kinase Deficiency.

Munekane A, Ohsawa Y, Fukuda T, Nishimura H, Nishimatsu SI, Sugie H, Saito Y, Nishino I, Sunada Y. Munekane A, et al. Among authors: saito y. Intern Med. 2022 Apr 15;61(8):1241-1245. doi: 10.2169/internalmedicine.8137-21. Epub 2021 Oct 5. Intern Med. 2022. PMID: 34615823 Free PMC article.

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. Among authors: saito y. 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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