Seizures and electroencephalographic findings in CDKL5 mutations: Case report and review-Reference-Cited by-同舟云学术

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Seizures and electroencephalographic findings in CDKL5 mutations: Case report and review

Published:2007-05 Issue:4 Volume:29 Page:239-242
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Grosso S.,Brogna A.,Bazzotti S.,Renieri A.,Morgese G.,Balestri P.

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference17 articles.

1. Annotation: Rett syndrome: recent progress and implications for research and clinical practice;Kerr;J Child Psychol Psychiatry,2002

2. The clinical pattern of the Rett syndrome;Hanefeld;Brain Dev,1985

3. Atypical forms of Rett syndrome;Goutieres;Am J Med Genet Suppl,1986

4. Disruption of the serine/threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation;Kalscheuer;Am J Hum Genet,2003

5. Early onset seizures and Rett-like features associated with mutations in CDKL5;Evans;Eur J Hum Genet,2005

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1. First report of Tunisian patients with CDKL5‐related encephalopathy;Epilepsia Open;2023-09-13

2. Epileptic spasms in CDKL5 deficiency disorder: Delayed treatment and poor response to first‐line therapies;Epilepsia;2023-05-15

3. CDKL5-associated developmental and epileptic encephalopathy: A long-term, longitudinal electroclinical study of 22 cases;Epilepsy Research;2023-02

4. INVESTIGATION OF CDKL5 GENE MUTATIONS IN AUTISTIC PATIENTS ACCOMPANIED WITH INTRACTABLE SEIZURES, AUTISTIC DISORDER AND SEIZURE IN INFANCY AND EARLY CHILDHOOD;Cumhuriyet Medical Journal;2022-06-18

5. CDKL5 Deficiency Disorder-Related Epilepsy: A Review of Current and Emerging Treatment;CNS Drugs;2022-05-28

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