Kwok‐Yin Chan

Expanding Phenotype and Clinical Analysis of Tyrosine Hydroxylase Deficiency

Wai-lan Yeung, Virginia Wong, Kwok‐Yin Chan et al. · Journal of Child Neurology · 2010 · 44 citations

Mendelian Disorder, Neurological Disorder, Genetic Disorder +13

Non-invasive urinary screening for aromatic l-amino acid decarboxylase deficiency in high-prevalence areas: A pilot study

Han‐Chih Hencher Lee, Chi-Kong Lai, Kin-Cheong Eric Yau et al. · Clinica Chimica Acta · 2011 · 22 citations

Pilot Study, Urological Research, Urology +6

DNA-Based Diagnosis of Isolated Sulfite Oxidase Deficiency by Denaturing High-Performance Liquid Chromatography

Ching‐Wan Lam, Chi Kong Li, Chi-Kong Lai et al. · Molecular Genetics and Metabolism · 2002 · 19 citations

Biochemistry, Dna-based Diagnosis, High-performance Liquid Chromatography +7

Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese

Chloe Miu Mak, C. W. Lam, Tak-Shing Siu et al. · Molecular Genetics and Metabolism · 2009 · 18 citations

Molecular Characterization, Biochemistry, Medicine +5

Infantile isolated sulphite oxidase deficiency in a Chinese family: a rare neurodegenerative disorder.

Kwok‐Yin Chan, C K Li, Chi-Kong Lai et al. · PubMed · 2002 · 17 citations

Oxidative Stress, Intensive Care Unit, Rare Neurodegenerative Disorder +16