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Historic, Clinical, and Prognostic Features of Epileptic Encephalopathies Caused by CDKL5 Mutations

  • Published:2012-02 Issue:2 Volume:46 Page:101-105
  • ISSN:0887-8994
  • Container-title:Pediatric Neurology
  • language:en
  • Short-container-title:Pediatric Neurology

Author:

Moseley Brian D.,Dhamija Radhika,Wirrell Elaine C.,Nickels Katherine C.

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference30 articles.

1. Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations;Deprez;Neurology,2010

2. West syndrome associated with 14q12 duplications harboring FOXG1;Striano;Neurology,2011

3. EEG features and epilepsy in MECP2-mutated patients with the Zappella variant of Rett syndrome;Buoni;Clin Neurophysiol,2010

4. Severe mental retardation, seizures, and hypotonia due to deletions of MEF2C;Nowakowska;Am J Med Genet [B] Neuropsychiatr Genet,2010

5. Phospholipase C beta 1 deficiency is associated with early-onset epileptic encephalopathy;Kurian;Brain J Neurol,2010
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