Medical Attitudes Survey for Female Dystrophinopathy Carriers in Japan-Reference-Cited by-同舟云学术

Medical Attitudes Survey for Female Dystrophinopathy Carriers in Japan

Published:2018-08-15 Issue:16 Volume:57 Page:2325-2332
ISSN:0918-2918
Container-title:Internal Medicine
language:en
Short-container-title:Intern. Med.

Author:

Kobayashi Michio¹,Hatakeyama Tomoyuki¹,Ishizaki Masatoshi²,Adachi Katsuhito³,Morita Mizuki⁴,Yonemoto Naohiro⁵,Matsumura Tsuyoshi⁶,Toyoshima Itaru¹,Kimura En⁷

Affiliation:

1. Department of Neurology, Akita National Hospital, Japan

2. Department of Neurology, Kumamoto Saishunso National Hospital, Japan

3. Department of Internal Medicine, Tokushima National Hospital, Japan

4. Department of Biorepository Research and Networking, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Japan

5. Department of Biostatics, Kyoto University, Japan

6. Department of Neurology, Toneyama National Hospital, Japan

7. Translational Medical Center, National Center of Neurology and Psychiatry, Japan

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Link

https://www.jstage.jst.go.jp/article/internalmedicine/57/16/57_0163-17/_pdf

Reference21 articles.

1. 1. Lee T, Takeshima Y, Kusunoki N, et al. Differences in carrier frequency between mothers of Duchenne and Becker muscular dystrophy patients. J Hum Genet 59: 46-50, 2014.

2. 2. Hoogerwaard EM, Bakker E, Ippel PF, et al. Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in The Netherlands: a cohort study. Lancet 353: 2116-2119, 1999.

3. 3. Politano L, Nigro V, Nigro G, et al. Development of cardiomyopathy in female carriers of Duchenne and Becker muscular dystrophies. JAMA 275: 1335-1338, 1996.

4. 4. Imbornoni L, Price ET, Andrews J, Meaney FJ, Ciafaloni E, Cunniff C. Diagnostic and clinical characteristics of early-manifesting females with Duchenne or Becker muscular dystrophy. Am J Med Genet A 164a: 2769-2774, 2014.

5. 5. Hori H, Maeda Y, Ishizaki M, et al. A carrier with de novo Mutation in the dystrophin gene whose myopathic symptoms became seriously progressive after pregnancy and delivery. Muscle Nerve 52: 913-914, 2015.

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