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Publications by D. M. Sproule

Natural History of MELAS Associated With Mitochondrial DNA M.3243A>G Genotype

English

Monitoring of Cerebral Vasodilatory Capacity With Transcranial Doppler Carbon Dioxide Inhalation in Patients With Severe Carotid Artery Disease

Cardiovascular Medicine

Specialized Nursing

English

Related publications

Glucose Metabolism Derangements in Adults With the MELAS M.3243A>G Mutation

Molecular Medicine

Molecular Biology

English

Mitochondrial DNA M.3243A > G Heteroplasmy Affects Multiple Aging Phenotypes and Risk of Mortality

Scientific Reports

Multidisciplinary

English

Gastro-Intestinal Involvement in M.3243A>G-Associated Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes

Internal Medicine

Internal Medicine

English

De Novo Mutation of M.3243A>G Together With M.16093T>C Associated With Atypical Clinical Features in a Pedigree With MIDD Syndrome

Journal of Diabetes Research

English

Fear of Disease Progression in Carriers of the M.3243A > G Mutation

Orphanet Journal of Rare Diseases

English

Natural History and Genotype-Phenotype Correlations in 72 Individuals With SATB2 -Associated Syndrome

American Journal of Medical Genetics, Part A

English

Reduced Bone Mineral Density in M.3243A > G Carriers May Be Multifactorial

Journal of Bone and Mineral Research

Sports Medicine

English

Authors' Reply to 'Heteroplasmy of the M.3243A>G Mutation May Influence Phenotypic Heterogeneity'

Internal Medicine

Internal Medicine

English

Fine Mapping of Mitochondrial RNAs Derived From the mtDNA Region Containing a Point Mutation Associated With MELAS

Nucleic Acids Research

English