Y. Chan

发表

Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneity

Y. Lau, S. Fan, Ching-lung Lai, 2008, Journal of Human Genetics.

Factitious thyrotoxicosis and herbal dietary supplement for weight reduction

C. Lai, W. Poon, W. Mak, 2008, Clinical toxicology.

Maternally inherited Leigh syndrome: an unusual cause of infantile apnea

C. Lam, Y. Yuen, W. Siu, 2010, Sleep and Breathing.

DNA-based diagnosis of isolated sulfite oxidase deficiency by denaturing high-performance liquid chromatography.

C. Lam, Kwok-Yin Chan, Chi-kong Lai, 2002, Molecular genetics and metabolism.

Proteomics investigation on aristolochic acid nephropathy: a case study on rat kidney tissues

Z. Cai, Y. Mak, W. Poon, 2011, Analytical and bioanalytical chemistry.

Young-Onset Parkinsonism in a Hong Kong Chinese Man With Adult-Onset Hallervorden–Spatz Syndrome

C. Lam, Hencher Han-Chih Lee, C. Mak, 2011, The International journal of neuroscience.

Clinical and pathological characterization of FLNC‐related myofibrillar myopathy caused by founder variant c.8129G>A in Hong Kong Chinese

N. Pan, C. Lam, K. Lee, 2020, Clinical genetics.

DNA-based diagnosis of methylmalonic aciduria and homocystinuria, cblC type in a Chinese patient presenting with mild developmental delay.

C. Lam, Kwok-Yin Chan, Chi-kong Lai, 2007, Clinica chimica acta; international journal of clinical chemistry.

Novel mutations in the BCHE gene in patients with no butyrylcholinesterase activity.

C. Lam, K. Au, C. Shek, 2005, Clinica chimica acta; international journal of clinical chemistry.

Hepatitis induced by Teucrium viscidum

W. Poon, Y. Chan, C. Lai, 2008, Clinical toxicology.

Isolation of the uterotonic principle from Leonurus artemisia, the Chinese motherwort.

H. Yeung, Y. M. Cheung, J. C. Hwang, 1976, The American journal of Chinese medicine.

Simultaneous fluorescence detection of fecal urobilins and porphyrins by reversed-phase high-performance thin-layer chromatography.

C. Lam, C. Lai, Y. Chan, 1998, Clinical chemistry.

Non-invasive screening of HLA-DPA1 and HLA-DPB1 alleles for persistent hepatitis B virus infection: susceptibility for vertical transmission and toward a personalized approach for vaccination and treatment.

C. Lam, P. Chan, W. Poon, 2011, Clinica chimica acta; international journal of clinical chemistry.

Confirmation of gelsemium poisoning by targeted analysis of toxic gelsemium alkaloids in urine.

Y. Chan, C. Lai, 2009, Journal of analytical toxicology.

High-performance thin-layer chromatography of free porphyrins for diagnosis of porphyria.

C. Lai, Y. Chan, C. Lam, 1994, Clinical chemistry.

Quantification of aristolochic acid-derived DNA adducts in rat kidney and liver by using liquid chromatography-electrospray ionization mass spectrometry.

Z. Cai, W. Chan, O. Schmitz, 2008, Mutation research.

A novel mutation, Y255X, of the ARSB gene in a Chinese family with mucopolysaccharidosis type VI.

C. Lam, A. Chan, C. Shek, 2004, Chinese medical journal.

A novel mitofusin 2 gene mutation causing Charcot-Marie-Tooth type 2A disease in a Chinese family.

C. Ching, Y. Chan, K. Lau, 2010, Chinese medical journal.

Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneity

Y. Lau, S. Fan, S. Tam, 2008, Journal of Human Genetics.

Novel donor splice site mutation of ABCG5 gene in sitosterolemia.

C. Lam, S. Tong, Y. Chan, 2002, Molecular genetics and metabolism.

A new approach for the sensitive determination of DNA adduct of aristolochic acid II by using high-performance liquid chromatography with fluorescence detection.

Z. Cai, W. Chan, W. Poon, 2009, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Acute renal failure associated with prolonged intake of slimming pills containing anthraquinones.

C. Lai, W. Poon, K. Leung, 2006, Hong Kong medical journal = Xianggang yi xue za zhi.

Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome.

C. Lam, Y. Yuen, S. Tong, 2006, Clinica chimica acta; international journal of clinical chemistry.

Ethnic-specific splicing mutation of the carnitine-acylcarnitine translocase gene in a Chinese neonate presenting with sudden unexpected death.

Y. Mak, C. Lam, Y. Yuen, 2003, Chinese medical journal.

Clinical and Genetic Characterization of Huntington Disease among Hong Kong Chinese – A 5-year Review

K. Au, W. Poon, C. Mak, 2018 .

Circulating fluorocytes at the first attack of acute intermittent porphyria: a missing link in the pathogenesis.

M. Tsang, C. Lam, C. Mak, 2011, Clinica chimica acta; international journal of clinical chemistry.

Novel splicing mutation of the PPOX gene (IVS10 + 1G-->A) detected by denaturing high-performance liquid chromatography.

C. Lam, C. Lai, Y. Yuen, 2001, Clinica chimica acta; international journal of clinical chemistry.

Hidden aconite poisoning: identification of yunaconitine and related aconitum alkaloids in urine by liquid chromatography-tandem mass spectrometry.

W. Poon, Y. Chan, C. Lai, 2006, Journal of Analytical Toxicology.

Novel mutation and polymorphisms of the HMBS gene detected by denaturing HPLC.

K. L. Choi, A. Lo, C. Lam, 2001, Clinical chemistry.