Valeriy Levandovskiy

Mutations in Iron-Sulfur Cluster Scaffold Genes NFU1 and BOLA3 Cause a Fatal Deficiency of Multiple Respiratory Chain and 2-Oxoacid Dehydrogenase Enzymes

Jessie M. Cameron, Alexandre Janer, Valeriy Levandovskiy et al. · The American Journal of Human Genetics · 2011 · 270 citations · Full text

Fatal Deficiency, Biochemistry, Iron Metabolism +11

Identification of a novel mutation in GYS1 (muscle-specific glycogen synthase) resulting in sudden cardiac death, that is diagnosable from skin fibroblasts

Jessie M. Cameron, Valeriy Levandovskiy, Nevena MacKay et al. · Molecular Genetics and Metabolism · 2009 · 81 citations

Cardiac Muscle, Cardiomyopathy, Fibrosis +9

Disruption of a mitochondrial RNA-binding protein gene results in decreased cytochrome <i>b</i> expression and a marked reduction in ubiquinol–cytochrome <i>c</i> reductase activity in mouse heart mitochondria

Fenghao Xu, Cameron Ackerley, Mary C. Maj et al. · Biochemical Journal · 2008 · 79 citations

Heart Failure, Molecular Biology, Mitochondrial Biology +16

Pyruvate Dehydrogenase Phosphatase Deficiency: Identification of the First Mutation in Two Brothers and Restoration of Activity by Protein Complementation

Mary C. Maj, Neviana MacKay, Valeriy Levandovskiy et al. · The Journal of Clinical Endocrinology & Metabolism · 2005 · 64 citations · Full text

Novel mutations in dihydrolipoamide dehydrogenase deficiency in two cousins with borderline‐normal PDH complex activity

Jessie M. Cameron, Valeriy Levandovskiy, Neviana MacKay et al. · American Journal of Medical Genetics Part A · 2006 · 57 citations