Rare Diseases
Records 1 - 4 (of 4 Records) |
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The International SCN8A Patient Registry: A Scientific Resource to Advance the Understanding and Treatment of a Rare Pediatric Neurodevelopmental Syndrome. Jennifer G Andrews et al. J Registry Manag 2023 50(1) 4-10 |
KCNQ2 - Related Epilepsy: geno - phenotype relationship with tailorized anti seizures medication (ASM): Systematic review. Raffaele Falsaperla et al. Neuropediatrics 2023 |
Genome sequencing of 320 Chinese children with epilepsy: a clinical and molecular study. Zou Dongfang et al. Brain : a journal of neurology 2021 |
Determining the best candidates for next-generation sequencing-based gene panel for evaluation of early-onset epilepsy. Lee Jiwon et al. Molecular genetics & genomic medicine 2020 Jul e1376 |