A detailed investigation of maternally inherited diabetes and deafness (MIDD) including clinical characteristics, C-peptide secretion, HLA-DR and -DQ status and autoantibody pattern-Reference-Cited by-同舟云学术

A detailed investigation of maternally inherited diabetes and deafness (MIDD) including clinical characteristics, C-peptide secretion, HLA-DR and -DQ status and autoantibody pattern

Published:2009-02 Issue:2 Volume:25 Page:127-135
ISSN:1520-7552
Container-title:Diabetes/Metabolism Research and Reviews
language:en
Short-container-title:Diabetes Metab. Res. Rev.

Author:

Hosszúfalusi Nóra,Karcagi Veronika,Horváth Rita,Palik Éva,Várkonyi Judit,Rajczy Katalin,Prohászka Zoltán,Szentirmai Csaba,Karádi István,Romics László,Pánczél Pál

Publisher

Wiley

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference28 articles.

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2. Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR) gene;van den Ouweland;Diabetes,1994

3. Mutation in mitochondrial tRNA(Leu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness;van den Ouweland;Nat Genet,1992

4. Maternally inherited diabetes and deafness: a new diabetes subtype;Maassen;Diabetologia,1996

5. Maternally inherited diabetes and deafness: a multicenter study;Guillausseau;Ann Intern Med,2001

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1. Maternally inherited diabetes and deafness (MIDD): An uncommon but important cause of diabetes;Endocrine and Metabolic Science;2021-03

2. Mitochondrialer Diabetes;Journal für Klinische Endokrinologie und Stoffwechsel;2019-06

3. The clinical characteristics of patients with mitochondrial tRNA Leu(UUR)m.3243A > G mutation: Compared with type 1 diabetes and early onset type 2 diabetes;Journal of Diabetes and its Complications;2017-08

4. Low prevalence of patients with mitochondrial disease in the German/Austrian DPV diabetes registry;European Journal of Pediatrics;2015-12-15

5. Serum FGF21 levels in adult m.3243A>G carriers: Clinical implications;Neurology;2014-06-06