Survey of patients with advanced-stage Okinawa-type neurogenic muscular atrophy (hereditary motor and sensory neuropathy with proximal dominant involvement: HMSN-P)-Reference-Cited by-同舟云学术

Survey of patients with advanced-stage Okinawa-type neurogenic muscular atrophy (hereditary motor and sensory neuropathy with proximal dominant involvement: HMSN-P)

Published:2022 Issue:2 Volume:62 Page:152-156
ISSN:0009-918X
Container-title:Rinsho Shinkeigaku
language:en
Short-container-title:Rinsho Shinkeigaku

Author:

Taniguchi Masahiko¹,Yorishima Yuki²,Shoji Hiroshi²,Ide Makoto³,Kumura Yusuke⁴,Kunisaki Keisuke⁴

Affiliation:

1. Department of Surgery, St. Mary’s Hospital

2. Department of Neurology, St. Mary’s Hospital

3. Healthcare-Center, St. Mary’s Hospital

4. Rehabilitation Unit, St. Mary’s Hospital

Publisher

Societas Neurologica Japonica

Subject

Neurology (clinical)

Link

https://www.jstage.jst.go.jp/article/clinicalneurol/62/2/62_cn-001576/_pdf

Reference10 articles.

1. 1) 湯浅龍彦，水町真知子，若林佑子ら．筋萎縮性側索硬化症のインフォームド・コンセント．医療 2002;56;338-343.

2. 2) 荻野美恵子．日本におけるALS終末期．臨床神経 2008;48:973-975.

3. 3) 京都新聞社説：ALS嘱託殺人，生きようと思う社会に．2020年7月28日．

4. 4) Takashima H, Nakagawa M, Nakahara K, et al. A new type of hereditary motor and sensory neuropathy linked to chromosome. Ann Neurol 1997;41:771-780.

5. 5) Fujisaki N, Suwazono S, Suehara M, et al. The natural history of hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) in 97 Japanese patients. Intractable Rare Dis Res 2018;7:7-12.

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1. Re-survey of 16 Japanese patients with advanced-stage hereditary motor sensory neuropathy with proximal dominant involvement (HMSN-P): Painful muscle cramps for early diagnosis;Intractable & Rare Diseases Research;2023-08-31