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Publications by Ralitza H. Gavrilova

Loss-Of-Function Mutations in UDP-Glucose 6-Dehydrogenase Cause Recessive Developmental Epileptic Encephalopathy

Nature Communications

Molecular Biology

English

Clinical Spectrum of STX1B-related Epileptic Disorders

English

Novel GRN Mutation Presenting as an Aphasic Dementia and Evolving Into Corticobasal Syndrome

Neurology: Genetics

English

Mitochondrial Diseases in North America

Neurology: Genetics

English

Anesthetic Considerations in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome: A Case Series

Canadian Journal of Anaesthesia

English

Developmental Delay, Coarse Facial Features, and Epilepsy in a Patient With EXT2 Gene Variants

Clinical Case Reports

English