Showing results 1 to 6 of 6
Title | Author(s) | Issue Date | |
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A common PRRT2 mutation in familial paroxysmal kinesigenic dyskinesia in Hong Kong: a case series of 16 patients Journal:Hong Kong Medical Journal | 2016 | ||
Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese Journal:Molecular Genetics and Metabolism | 2010 | ||
Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiency Journal:Journal of Child Neurology | 2011 | ||
Galactorrhea-A strong clinical clue towards the diagnosis of neurotransmitter disease Journal:Brain and Development | 2006 | ||
Isolated persistent elevation of alanine transaminase for early diagnosis of pre-symptomatic Wilson’s disease in Chinese children Journal:World Journal of Pediatrics | 2013 | ||
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