The spectrum of clinical presentation, diagnosis, and management of mitochondrial forms of diabetes-Reference-Cited by-同舟云学术

The spectrum of clinical presentation, diagnosis, and management of mitochondrial forms of diabetes

Published:2014-10-20 Issue:1 Volume:16 Page:1-9
ISSN:1399-543X
Container-title:Pediatric Diabetes
language:en
Short-container-title:Pediatr Diabetes

Author:

Karaa Amel¹^ORCID,Goldstein Amy²

Affiliation:

1. Neurogenetics Clinic, Neurology and Clinical Genetics; Massachusetts General Hospital, Harvard Medical School; Boston MA USA

2. Neurogenetics & Metabolism, Division of Child Neurology, Children's Hospital of Pittsburgh of UPMC; University of Pittsburgh School of Medicine; Pittsburgh PA USA

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health,Internal Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/pedi.12223/fullpdf

Reference35 articles.

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2. Endocrine disorders in mitochondrial disease;Schaefer;Mol Cell Endocrinol,2013

3. Treatment of mitochondrial electron transport chain disorders: a review of clinical trials over the past decade;Kerr;Mol Genet Metab,2010

4. m.3243A>G mutation in mitochondrial DNA leads to decreased insulin sensitivity in skeletal muscle and to progressive beta-cell dysfunction;Lindroos;Diabetes,2009

5. Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation;Velho;Diabetes,1996

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