Kyphoscoliosis and easy fatigability in a 14-year-old boy-Reference-Cited by-同舟云学术

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Kyphoscoliosis and easy fatigability in a 14-year-old boy

Published:2014-08-28 Issue:1 Volume:35 Page:91-93
ISSN:0919-6544
Container-title:Neuropathology
language:en
Short-container-title:Neuropathology

Author:

Tanboon Jantima¹,Hayashi Yukiko K.²³⁴,Nishino Ichizo³⁴,Sangruchi Tumtip¹

Affiliation:

1. Department of Pathology; Faculty of Medicine; Siriraj Hospital; Mahidol University; Bangkok Thailand

2. Department of Neurophysiology; Tokyo Medical University; Tokyo Japan

3. Department of Neuromuscular Research; National Institute of Neuroscience; National Center of Neurology and Psychiatry; Tokyo Japan

4. Department of Clinical Development; Translational Medical Center; National Center of Neurology and Psychiatry; Tokyo Japan

Funder

Ministry of Health Labour and Welfare, Japan

National Center of Neurology and Psychiatry, Japan

Publisher

Wiley

Subject

Neurology (clinical),General Medicine,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/neup.12147/fullpdf

Reference9 articles.

1. Novel TPM3 mutation in a family with cap myopathy and review of the literature;Schreckenbach;Neuromuscul Disord,2014

2. Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies;Marttila;Hum Mutat,2014

3. “Cap disease” - a failure in the correct muscle fibre formation;Fidzianska;J Neurol Sci,2002

4. “Cap myopathy”: case report of a family;Cuisset;Neuromuscul Disord,2006

5. New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutations;Ohlsson;Neurology,2008

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