Dr García-Cazorla is a Paediatric Neurologist at the Sant Joan de Déu Barcelona Children's Hospital, in Barcelona. She is an expert in rare neurometabolic and neurogenetic disorders.
Dr Cazorla obtained her degree in Medicine from the University of Barcelona. She then completed her clinical and scientific training in Inborn Errors of Metabolism and Neurometabolic Disorders at the Hospital Necker, in Paris, and at the University of Columbia in New York (post-doctoral fellowship). She has been an Associate Professor at the University of Barcelona since 2012.
She is currently the coordinator of the Neurometabolic Disorders Unit and the Lead Researcher at the Neurology Laboratory (Synaptic Metabolism Lab). She is a member of the CIBERER Network, a member of Scientific Committee of the Recordati Rare Diseases Foundation, and the coordinator of the subgroup of neurotransmitter related disorders at the MetabERN. Her research interests include neurotransmission mechanisms and neuronal communication in inborn metabolic diseases as well as the development of new therapies for these rare diseases.