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Results 1 - 6 of 6 for "Childhood-onset" epilepsy syndrome
  1. ... Ohta H, Abiru K, Nakano K, Oka E. Childhood-onset epilepsy associated with ... Lennox-Gastaut syndrome, and GPR56 gene mutations. Epilepsia. 2009 Jun;50( ...
  2. ... Vincent A, Wilson M. Incidence and phenotypes of childhood-onset genetic ... Transporter Type 1 Deficiency Syndrome. 2002 Jul 30 [updated 2018 Mar 1]. In: ...
  3. ... Vincent A, Wilson M. Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohort. Brain. 2019 ...
  4. ... family history of MERRF. Fukuhara disease MERRF MERRF syndrome Myoclonic epilepsy associated with ragged-red fibers Myoencephalopathy ragged-red fiber disease Genetic Testing Registry: MERRF syndrome MERRF ... MYOCLONIC EPILEPSY ASSOCIATED WITH RAGGED-RED FIBERS; MERRF PubMed Blakely ...
  5. ... person's mother (maternal inheritance). DRPLA Haw River syndrome Myoclonic epilepsy with choreoathetosis Naito-Oyanagi disease NOD Genetic Testing Registry: Dentatorubral-pallidoluysian atrophy Dentatorubral pallidoluysian atrophy ... Roses AD, Lee JE, Hulette C, Pericak-Vance MA, Vance JM. The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family. ...
  6. ... infantile convulsions and choreoathetosis (ICCA) and ICCA-related syndromes. J Med Genet. ... paroxysmal kinesigenic dyskinesia with PRRT2 gene mutations. Dev ...