Familial Pernicious Chronic Intestinal Pseudo-obstruction with a Mitochondrial DNA A3243G Mutation
Author:
Affiliation:
1. Department of Neurology, TOYOTA Memorial Hospital, Japan
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/56/9/56_56.7753/_pdf
Reference26 articles.
1. 1. Ma Y, Fang F, Cao Y, et al. Clinical features of mitochondrial DNA m.3243A>G mutation in 47 Chinese families. J Neurol Sci 291: 17-21, 2010.
2. 2. Hom XB, Lavine JE. Gastrointestinal complications of mitochondrial disease. Mitochondrion 4: 601-607, 2004.
3. 3. Ohkubo H, Iida H, Takahashi H, et al. An epidemiologic survey of chronic intestinal pseudo-obstruction and evaluation of the newly proposed diagnostic criteria. Digestion 86: 12-19, 2012.
4. 4. Lee YC, Liu CS, Wu HM, Wang PS, Chang MH, Soong BW. The 'hot cross bun' sign in the patients with spinocerebellar ataxia. Eur J Neurol 16: 513-516, 2009.
5. 5. Sudarsky L, Plotkin GM, Logigian EL, Johns DR. Dystonia as a presenting feature of the 3243 mitochondrial DNA mutation. Mov Disord 14: 488-491, 1999.
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