Dr. Leung obtained her undergraduate degree in biochemical sciences from Harvard University. While attending medical school at Duke University, she completed a year-long research fellowship studying genetic markers of late-onset Alzheimer’s disease at the National Institute on Aging as part of the NIH Clinical Research Training Program. She completed her neurology residency and clinical neurophysiology fellowship at Stanford University Medical Center, and is currently a Ph.D. candidate in the graduate training program in clinical investigation at the Johns Hopkins Bloomberg School of Public Health. Dr. Leung joined the Center for Genetic Muscle Disorders at the Kennedy Krieger Institute as a translational research fellow in 2010 and was appointed to the faculty in 2014. Her clinic specializes in electromyography and the diagnosis and treatment of hereditary muscle diseases. Dr. Leung’s research focuses on the development of imaging biomarkers and outcome measures for muscle diseases. She is the principal investigator for a longitudinal cohort study of whole-body MRI in facioscapulohumeral muscular dystrophy. Dr. Leung is also a site principal investigator for the Ionis-DMPKRx trial, a phase Ib/IIa clinical trial of a novel RNA-based therapy for myotonic muscular dystrophy. Dr. Leung is rated as an Advanced provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. Her top areas of expertise are Facioscapulohumeral Muscular Dystrophy (FSHD), Dysferlinopathy, Limb-Girdle Muscular Dystrophy Type 2I, and Limb-Girdle Muscular Dystrophy.

Dr. Hilary Vernon is a Professor of Genetic Medicine and pediatrics at the Johns Hopkins University School of Medicine. She is also an attending physician at Kennedy Krieger Institute. Hilary Vernon has expertise in treating inborn errors of metabolism and mitochondrial disorders. She is the director of the Mitochondrial Care Center at The Johns Hopkins Hospital and the Barth Syndrome Interdisciplinary Clinic at the Kennedy Krieger Institute. Her research interests include understanding intermediary metabolism in Barth syndrome and in disorders of branch chain amino acid metabolism. Dr. Vernon also co-directs the Department of Genetic Medicine Clinical Trials Unit, and is the principal investigator on multiple clinical trials for rare diseases. Dr. Vernon received her medical degree and doctorate from Rutgers University, New Brunswick, New Jersey. She completed residencies in genetics and pediatrics at The Johns Hopkins University, and a fellowship in clinical laboratory biochemical genetics at The Johns Hopkins University. Dr. Vernon was recognized with the 2010 Francis F. Schwentker Award for Excellence in Research at Johns Hopkins University and the 2011 James B. Sidbury Jr. Fellowship in Biochemical Genetics at Johns Hopkins University. Dr. Vernon is rated as an Advanced provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. Her top areas of expertise are Methylmalonic Acidemia, Propionic Acidemia, Infantile Neutropenia, Progressive External Ophthalmoplegia, and Gastrostomy.

Dr. Ricardo Roda earned a combined MD/PhD degree from University of Rochester and completed an adult neurology residency, followed by a clinical neuromuscular fellowship at Johns Hopkins University School of Medicine. During residency, Dr. Roda developed a special interest in both auto-immune disorders and genetic disorders. Following residency, he spent three years in neurogenetics branch of National Institute of Neurological Disorders and Stroke (NINDS) working with Dr. Craig Blackstone, focusing on the use of the newer DNA sequencing techniques in genetic diagnosis, and in establishing genotype/phenotype correlations neuromuscular disorders. His current clinical interests include developing testing strategies for undiagnosed genetic disorders and myasthenia gravis. Dr. Roda is rated as an Experienced provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. His top areas of expertise are Spastic Paraplegia Type 7, Hereditary Spastic Paraparesis, Myasthenia Gravis, and Spastic Paraplegia Type 2.

Hind Alsharhan is a Medical Genetics provider in Baltimore, Maryland. Dr. Alsharhan is rated as an Experienced provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. Her top areas of expertise are ALG3-CDG, Ornithine Transcarbamylase Deficiency, Coenzyme Q Cytochrome C Reductase Deficiency, and Phenylketonuria (PKU).

Carol Greene is a Pediatrics provider in Baltimore, Maryland. Dr. Greene is rated as an Experienced provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. Her top areas of expertise are Musculocontractural Ehlers-Danlos Syndrome (mcEDS), Phenylketonuria (PKU), Increased Head Circumference, and MELAS Syndrome.

Narender Bharaj is a primary care provider, practicing in Internal Medicine in Parkville, Maryland. Dr. Bharaj is rated as an Experienced provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. His top areas of expertise are Dementia, Anemia, Hypertension, and Glucocorticoid-Remediable Aldosteronism.

David Adams is a Medical Genetics specialist and a Pediatrics provider in Bethesda, Maryland. Dr. Adams is rated as an Experienced provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. His top areas of expertise are Hermansky-Pudlak Syndrome, Oculocutaneous Albinism Type 2, Oculocutaneous Albinism, and Oculocutaneous Albinism Type 1.

Peter Mcguire is a Medical Genetics specialist and a Pediatrics provider in Bethesda, Maryland. Dr. Mcguire is rated as an Experienced provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. His top areas of expertise are Ornithine Transcarbamylase Deficiency, Urea Cycle Disorders (UCD), Coenzyme Q Cytochrome C Reductase Deficiency, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency.

Robert Paschall is a Neurologist in Salisbury, Maryland. Dr. Paschall is rated as an Experienced provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. His top areas of expertise are Epilepsy, Stroke, Memory Loss, Seizures, and Gastrostomy. Dr. Paschall is currently accepting new patients.

Madhu Sachdev is a primary care provider, practicing in Family Medicine in North East, Maryland. Dr. Sachdev is rated as an Experienced provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. Her top areas of expertise are Bronchitis, Hypertension, Familial Hypertension, and Glucocorticoid-Remediable Aldosteronism. Dr. Sachdev is currently accepting new patients.

Elizabeth Streeten is an Endocrinologist and a Medical Genetics provider in Baltimore, Maryland. Dr. Streeten is rated as an Experienced provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. Her top areas of expertise are Osteoporosis-Pseudoglioma Syndrome, Osteoporosis, Gaucher Disease, and Gaucher Disease Type 3.