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Genotype-phenotype associations in SCN1A-related epilepsies
Download from www.researchgate.netNongenetic factors influence severity of episodic ataxia type 1 in monozygotic twins
Download from www.ncbi.nlm.nih.govGenotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)
Download from doi.orgTwo cases of sudden unexpected death in epilepsy in a GEFS+ family with an SCN1A mutation
Download from onlinelibrary.wiley.comSleep problems in children with neurological disorders.
Download from www.researchgate.netPsychosocial and intellectual functioning in childhood narcolepsy
Download from www.researchgate.netSpectrum of epilepsy in terminal 1p36 deletion syndrome
Download from www.researchgate.netClinical and Molecular Phenotype of Aicardi-Goutières Syndrome
Download from doi.orgDeletions or duplications in KCNQ2 can cause benign familial neonatal seizures
Download from www.ncbi.nlm.nih.govGenetics of epilepsy: epilepsy research foundation workshop report.
Download from doi.orgThe spectrum of SCN1A-related infantile epileptic encephalopathies
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