original ) (raw )Prevalence of 15 mitochondrial DNA mutations among type 2 diabetic patients with or without clinical characteristics of maternally inherited diabetes and deafness
Daisy Crispim
Arquivos Brasileiros de Endocrinologia & Metabologia, 2008
View PDFchevron_right
Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation
Rinki Murphy
Diabetic Medicine, 2008
View PDFchevron_right
A subtype of diabetes mellitus associated with a mutation in the mitochondrial gene
Yuzo Tanabe
Muscle & Nerve, 1995
View PDFchevron_right
Clinical features of diabetes mellitus with the mitochondrial DNA 3243 (A–G) mutation in Japanese: Maternal inheritance and mitochondria-related complications
Azuma Kanatsuka
Diabetes Research and Clinical Practice, 2003
View PDFchevron_right
Mitochondrial gene defects in patients with NIDDM
Mary Sweeney
Diabetologia, 1994
View PDFchevron_right
Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and/or deafness in an Italian family
Dario Iafusco , Luciana Rigoli
Diabetic Medicine, 2001
View PDFchevron_right
Involvement of nervous system in maternally inherited diabetes and deafness (MIDD) with the A3243G mutation of mitochondrial DNA
Yau-huei Wei
Acta Neurologica Scandinavica, 2001
View PDFchevron_right
A Novel Unstable Mutation in Mitochondrial DNA Responsible for Maternally Inherited Diabetes and Deafness
Meriame Abbassi
Diabetes Care, 2011
View PDFchevron_right
A pilot study of mitochondrial DNA point mutation A3243G in a sample of Croatian patients having type 2 diabetes mellitus associated with maternal inheritance
Jelka Gabrilovac
Acta Diabetologica, 2004
View PDFchevron_right
Mitochondrial tRNA Leu(UUR) gene mutation and maternally inherited diabetes mellitus in Pakistani population
maryam wahid
International Journal of Diabetes Mellitus, 2009
View PDFchevron_right
Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case–control study
Christine Bellanné-chantelot
Diabetologia, 2008
View PDFchevron_right
Prevalence and progression of diabetes in mitochondrial disease
Robert McFarland
Diabetologia, 2007
View PDFchevron_right
Whole mitochondrial genome screening of a family with maternally inherited diabetes and deafness (MIDD) associated with retinopathy: A putative haplotype associated to MIDD and a novel MT-CO2 m.8241T>G mutation
F. Fakhfakh
Journal of Diabetes and its Complications, 2017
View PDFchevron_right
The heteroplasmic m.14709T>C mutation in the tRNAGlu gene in two Tunisian families with mitochondrial diabetes
Emna Mkaouar-rebai , Najla Mezghani
Journal of Diabetes and its Complications, 2010
View PDFchevron_right
Macular dystrophy, diabetes, and deafness associated with a large mitochondrial dma deletion
Gabriel Coscas
American Journal of Ophthalmology, 1998
View PDFchevron_right
The search for mitochondrial tRNALeu(UUR) A3243G mutation among type 2 diabetes mellitus patients in the Nigerian population
Godwin Imade
African Journal of Biotechnology, 2011
View PDFchevron_right
Family Phenotypic Heterogeneity Caused by Mitochondrial DNA Mutation A3243G
Daniela R. Alves
Acta Médica Portuguesa
View PDFchevron_right
Maternally Inherited Diabetes and Deafness (MIDD) Syndrome: A Clinical and Molecular Genetic Study of a Taiwanese Family
Chia-wei Liou
2000
View PDFchevron_right
The Role of Heteroplasmy in the Diagnosis and Management of Maternally Inherited Diabetes and Deafness
Neena Xavier
Endocrine Practice, 2019
View PDFchevron_right
A new mitochondrial DNA mutation at 14577 T/C is probably a major pathogenic mutation for maternally inherited type 2 diabetes
Masato Tawata
Diabetes, 2000
View PDFchevron_right
Maternally inherited diabetes and deafness with a variable presentation across three generations within a pedigree, South Africa
Bettina Chale-Matsau
African journal of laboratory medicine, 2024
View PDFchevron_right
Maternally inherited diabetes pPatients from Manado and Jakarta posses A3243G mutation by PCR-Allele's specific amplification
Azmy Noer
chemistry.unpad.ac.id
View PDFchevron_right
Molecular genetic analysis of maternal inherited diabetes with deafness associated point mutatio
Fortune Journals
View PDFchevron_right
Functional and morphological abnormalities of mitochondria harbouring the tRNA Leu(UUR) mutation in mitochondrial DNA derived from patients with maternally inherited diabetes and deafness (MIDD) and progressive kidney disease
Giuseppe Attardi
Diabetologia, 1999
View PDFchevron_right
The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?
Daniele Orsucci
Journal of Neurology, 2014
View PDFchevron_right
Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness
Pascale Massin
Ophthalmology, 1999
View PDFchevron_right
Maternally-inherited diabetes with deafness (MIDD) and hyporeninemic hypoaldosteronism
Patricia Mory
Arquivos Brasileiros de Endocrinologia & Metabologia, 2012
View PDFchevron_right
Prevalence of Various Types Of Mitochondrial DNA Mutation In Type 2 Diabetes Mellitus In Pakistan
Maryam Pahlavan Sharif
2010
View PDFchevron_right
Mitochondrial tRNAleu(UUR) gene A3245G Mutationin Type 2 Diabetes
maryam wahid
2020
View PDFchevron_right