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Polymicrogyria and Intractable Epilepsy in Siblings With Knobloch Syndrome and Homozygous Mutation of COL18A1.
Charsar, Brittany A; Goldberg, Ethan M.
Afiliación
  • Charsar BA; Department of Neuroscience and Vickie and Jack Farber Institute for Neuroscience, Sidney Kimmel Medical College, and Jefferson College of Biomedical Sciences, Thomas Jefferson University, Philadelphia, Pennsylvania 19107. Electronic address: brittany.charsar@jefferson.edu.
  • Goldberg EM; Department of Pediatrics, Division of Neurology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania; Department of Neurology, The Perelman School of Medicine at The University of Pennsylvania, Philadelphia, Pennsylvania; Department of Neuroscience, The Perelman School of Medicine at The University of Pennsylvania, Pennsylvania.
Pediatr Neurol ; 76: 91-92, 2017 11.
Article en En | MEDLINE | ID: mdl-28950998

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Degeneración Retiniana / Desprendimiento de Retina / Discapacidades del Desarrollo / Colágeno Tipo VIII / Encefalocele / Polimicrogiria / Epilepsia Refractaria Tipo de estudio: Etiology_studies Idioma: En Año: 2017 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Degeneración Retiniana / Desprendimiento de Retina / Discapacidades del Desarrollo / Colágeno Tipo VIII / Encefalocele / Polimicrogiria / Epilepsia Refractaria Tipo de estudio: Etiology_studies Idioma: En Año: 2017 Tipo del documento: Article