Changes in the Treatment of Spinal Muscular Atrophy
Author:
Affiliation:
1. Department of Pediatrics and Child Health, Nihon University School of Medicine
Publisher
The Nihon University Medical Association
Subject
Applied Mathematics,General Mathematics
Link
https://www.jstage.jst.go.jp/article/numa/82/2/82_87/_pdf
Reference23 articles.
1. 1) Lefebvre S, Burglen L, Reboullet S, et al. Identification and characterization of a spinal muscular atrophy-determining gene. Cell 1995; 80: 155–165.
2. 2) 脊髄性筋萎縮症 (SMA) 診療の手引き編集委員会．脊髄性筋萎縮症 (SMA) 診療の手引き．メディカルレビュー 社，2022.10.31.
3. 3) Maeda K, Chong PF, Yamashita F, et al. Global central nervous system atrophy in spinal muscular atrophy type 0. Ann Neurol 2019; 86: 801–802.
4. 4) Yamamoto T, Sato H, Lai PS, et al. Intragenic mutations in SMN1 may contribute more significantly to clinical severity than SMN2 copy numbers in some spinal muscular atrophy (SMA) patients. Brain Dev 2017; 39: 763–773.
5. 5) Arnold WD, Kassar D, Kissel JT, et al. Spinal muscular atrophy: Diagnosis and management in a new therapeutic era. Muscle Nerve 2015; 51: 157–167.
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