Estudio de las epilepsias según la edad de inicio, controladas durante 3 años en una unidad de neuropediatría de referencia regional

Ochoa-Gómez, Laura; López-Pisón, Javier; Lapresta Moros, Carlos; Fuertes Rodrigo, Cristina; Fernando Martínez, Ruth; Samper-Villagrasa, Pilar; Monge-Galindo, Lorena; Peña-Segura, José Luis; García-Jiménez, María Concepción.
An. pediatr. (2003. Ed. impr.) ; 86(1): 11-19, ene. 2017. tab
Artículo en Español | IBECS (España) | ID: ibc-159130

Documentos relacionados

  1. Flexible Stoichiometry: Implications for KCNQ2- and KCNQ3-Associated Neurodevelopmental Disorders.
  2. Pathogenic variants in KCNQ2 cause intellectual deficiency without epilepsy: Broadening the phenotypic spectrum of a potassium channelopathy.
  3. Pitfalls of clinical exome and gene panel testing: alternative transcripts.
  4. Phenotypes of children with 20q13.3 microdeletion affecting KCNQ2 and CHRNA4.
  5. Potassium channelopathies associated with epilepsy-related syndromes and directions for therapeutic intervention.
  6. The ILAE classification of seizures and the epilepsies: Modification for seizures in the neonate. Position paper by the ILAE Task Force on Neonatal Seizures.
  7. Phenotypic Spectrum in a Family Sharing a Heterozygous <i>KCNQ3</i> Variant.
  8. Crisis neonatales y evolución a epilepsia en un hospital de tercer nivel
  9. [Clinical characteristics and genetic features of benign infantile epilepsy with PRRT2 mutation].
  10. Electroencephalography in neonatal epilepsies.