membro de AVALIAÇÃO, DESENVOLVIMENTO E IMPLEMENTAÇÃO DE TERAPIAS PARA DOENÇAS GENÉTICAS Grupo de Pesquisa Neurociência Aplicada a Saúde Mental e Doenças Neurodegenerativas da Criança e do Adolescente Grupo de Pesquisa
publicações selecionadas Clinical and Neurological Course of Tuberous Sclerosis Complex in Children and Adolescents Neurological Characteristics of Pediatric Glycogen Storage Disease Pediatric anti-N-methyl-D-aspartate receptor encephalitis mimicking glutaric aciduria type 1: A case report MUCOPOLYSACARIDOSIS TYPE IIIB MISDIAGNOSED AS AN AUTISTIC SPECTRUM DISORDER: A CASE REPORT AND LITERATURE REVIEW Diagnóstico tardio de síndrome de deleção 22q11.2 em criança com hipocalcemia sintomática: relato de caso Acute Childhood Viral Encephalitis in Southern Brazil Neurological, neurobehavioral, and radiological alterations in patients with mucopolysaccharidosis III (Sanfilippo's syndrome) in Brazil Neurodevelopmental regression, severe generalized dystonia, and metabolic acidosis caused by mutations Enzyme Replacement Therapy Decreases Left Ventricular Mass Index in Patients with Hunter Syndrome? GABAA receptor encephalitis associated with human parvovirus B19 virus infection: Case report Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features
