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

Glucose metabolism derangements in adults with the MELAS m.3243A>G mutation

(2014) Ayman W. El-Hattab et al.   MITOCHONDRION

The diagnosis and management of monogenic diabetes in children and adolescents

(2014) Oscar Rubio-Cabezas et al.   PEDIATRIC DIABETES

Mitochondria, endothelial cell function, and vascular diseases

(2014) Xiaoqiang Tang et al.   Frontiers in Physiology

The role of mitochondria in the aetiology of insulin resistance and type 2 diabetes

(2013) Sheree D. Martin et al.   BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS

Mitochondrial dysfunction and complications associated with diabetes

(2013) Rachel Blake et al.   BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS

Mitochondrial genetics

(2013) P. F. Chinnery et al.   BRITISH MEDICAL BULLETIN

Diabetes in Friedreich Ataxia

(2013) Miriam Cnop et al.   JOURNAL OF NEUROCHEMISTRY

The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?

(2013) Michelangelo Mancuso et al.   JOURNAL OF NEUROLOGY

Endocrine disorders in mitochondrial disease

(2013) Andrew M. Schaefer et al.   MOLECULAR AND CELLULAR ENDOCRINOLOGY

Mitochondrial DNA Depletion Syndromes: Review and Updates of Genetic Basis, Manifestations, and Therapeutic Options

(2013) Ayman W. El-Hattab et al.   Neurotherapeutics

Pearson syndrome: Unique endocrine manifestations including Neonatal Diabetes and adrenal insufficiency

(2012) T.B. Williams et al.   MOLECULAR GENETICS AND METABOLISM

High risk of severe cardiac adverse events in patients with mitochondrial m.3243A>G mutation

(2012) E. Malfatti et al.   NEUROLOGY

Role of genetics in resistance to type 1 diabetes

(2011) Jing Chen et al.   DIABETES-METABOLISM RESEARCH AND REVIEWS

Correction of the consequences of mitochondrial 3243A>G mutation in the MT-TL1 gene causing the MELAS syndrome by tRNA import into mitochondria

(2011) O. Z. Karicheva et al.   NUCLEIC ACIDS RESEARCH

MELAS and l-arginine therapy: pathophysiology of stroke-like episodes

(2010) Yasutoshi Koga et al.   Annals of the New York Academy of Sciences

The inheritance of pathogenic mitochondrial DNA mutations

(2009) L.M. Cree et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

The Clinical Variability of Maternally Inherited Diabetes and Deafness Is Associated with the Degree of Heteroplasmy in Blood Leukocytes

(2009) M. Laloi-Michelin et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Multisystem manifestations of mitochondrial disorders

(2009) Stefano Di Donato   JOURNAL OF NEUROLOGY

Treatment of mitochondrial electron transport chain disorders: A review of clinical trials over the past decade

(2009) Douglas S. Kerr   MOLECULAR GENETICS AND METABOLISM

URINE HETEROPLASMY IS THE BEST PREDICTOR OF CLINICAL OUTCOME IN THE m.3243A>G mtDNA MUTATION

(2009) R. G. Whittaker et al.   NEUROLOGY

m.3243A>G Mutation in Mitochondrial DNA Leads to Decreased Insulin Sensitivity in Skeletal Muscle and to Progressive  -Cell Dysfunction

(2008) M. M. Lindroos et al.   DIABETES