Gastrointestinal tract symptoms in Maternally Inherited Diabetes and Deafness (MIDD)
- 29 February 2004
- journal article
- Published by Elsevier BV in Diabetes & Metabolism
- Vol. 30 (1), 61-66
- https://doi.org/10.1016/s1262-3636(07)70090-3
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Intestinale Pseudoobstruktionen und Magenwandnekrose bei mitochondrialer MyopathieDeutsche Medizinische Wochenschrift (1946), 2002
- Mitochondrial Dysfunction and the Gastrointestinal SystemPublished by Springer Science and Business Media LLC ,2002
- Prevalence of Gastrointestinal Symptoms Associated With Diabetes MellitusArchives of Internal Medicine, 2001
- De novo mutation in the mitochondrial tRNALeu(UUR) gene (A3243G) with rapid segregation resulting in MELAS in the offspringJournal of Paediatrics and Child Health, 2001
- Adult-Onset MELASStroke, 1996
- Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafnessNature Genetics, 1992
- A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathiesNature, 1990
- Mitochondrial Myopathies with Necrotizing Encephalopathy of the Leigh TypePathology - Research and Practice, 1988
- Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with recurrent abdominal symptoms and coenzyme Q10 administration.Journal of Neurology, Neurosurgery & Psychiatry, 1987
- Ultrastructural study of the childhood mitochondrial myopathic syndrome associated with lactic acidosisEuropean Journal of Pediatrics, 1982