CDKL5 mutations as a cause of severe epilepsy in infancy: clinical and electroencephalographic long-term course in 4 patients.
about
Prevalence and onset of comorbidities in the CDKL5 disorder differ from Rett syndromeThere is variability in the attainment of developmental milestones in the CDKL5 disorder.Electroencephalogram of age-dependent epileptic encephalopathies in infancy and early childhood.Epileptic Encephalopathies-Clinical Syndromes and Pathophysiological Concepts.Two Siblings With a CDKL5 Mutation: Genotype and Phenotype Evaluation.Functional abilities in children and adults with the CDKL5 disorder.
P2860
CDKL5 mutations as a cause of severe epilepsy in infancy: clinical and electroencephalographic long-term course in 4 patients.
description
2012 nî lūn-bûn
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name
CDKL5 mutations as a cause of ...... ong-term course in 4 patients.
@en
CDKL5 mutations as a cause of ...... ong-term course in 4 patients.
@nl
type
label
CDKL5 mutations as a cause of ...... ong-term course in 4 patients.
@en
CDKL5 mutations as a cause of ...... ong-term course in 4 patients.
@nl
prefLabel
CDKL5 mutations as a cause of ...... ong-term course in 4 patients.
@en
CDKL5 mutations as a cause of ...... ong-term course in 4 patients.
@nl
P2093
P2860
P356
P1476
CDKL5 mutations as a cause of ...... long-term course in 4 patients
@en
P2093
Hiltrud Muhle
Ingo Helbig
Johanna Jähn
Rainer Boor
Sarah von Spiczak
Ulrich Stephani
P2860
P304
P356
10.1177/0883073812451497
P577
2012-07-25T00:00:00Z