Showing results 1 to 6 of 6
| Title | Author(s) | Issue Date | |
|---|---|---|---|
Anti-N-methyl-d-aspartate receptor encephalitis in children: Incidence and experience in Hong Kong Journal:Brain & Development | 2018 | ||
| 1-Jul-2023 | |||
Evaluation of the 18-month 'Pilot Study of Newborn Screening for Inborn Errors of Metabolism' in Hong Kong Journal:Hong Kong Journal of Paediatrics (New series) | 2020 | ||
Exome sequencing in paediatric patients with movement disorders [accepted - OJRD-D-20-00713R2] Journal:Orphanet Journal of Rare Diseases | 2021 | ||
Genetic diagnosis of severe myoclonic epilepsy of infancy (Dravet syndrome) with SCN1A mutations in the Hong Kong Chinese patients Journal:Hong Kong Medical Journal | 2011 | ||
Movement disorders associated with thiamine pyrophosphokinase deficiency: Intrafamilial variability in the phenotype Journal:Clinical Neurology and Neurosurgery | 2020 |