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You searched for: Author/Creator Ngoh, Adeline

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1. Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy. (2nd January 2018)

2. Delineation of the movement disorders associated with FOXG1 mutations. (10th May 2016)

4. Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis. Issue 5 (18th March 2016)

8. Severe infantile epileptic encephalopathy due to mutations in PLCB1: expansion of the genotypic and phenotypic disease spectrum. (29th March 2014)