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Ching-Wan Lam

Showing results (121-130 of 179) with videos related to

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Molecular Genetics and Metabolism Reports|December 7, 2023
CYP2U1: An emerging treatable neurometabolic disease with cerebral folate deficiency in 2 Chinese brothersSheila Suet-Na Wong, Liz Yuet-Ping Yuen, Elaine Kan, et al.
Plos Medicine|February 27, 2009
A 21-year-old pregnant woman with hypertension and proteinuriaAndrea Luk, Ronald C W Ma, Ching Wan Lam, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 5, 2023
Allan-Herndon-Dudley syndrome in Hong Kong: Implication for newborn screeningRachel Sze-Wan Yiu, Tsz-Ki Ling, Chun-Hung Ko, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 28, 2009
Diagnosis and spectrum of melamine-related renal disease: plausible mechanism of stone formation in humansChing-Wan Lam, Lawrence Lan, Xiaoyan Che, et al.
Journal of Child Neurology|September 9, 2010
Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiencyWai-Lan Yeung, Virginia C N Wong, Kwok-Yin Chan, et al.
Clinical and Translational Medicine|February 2, 2013
Development and promotion in translational medicine: perspectives from 2012 sino-american symposium on clinical and translational medicineMengjia Qian, Duojiao Wu, Ena Wang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 3, 2014
NMR-based urinalysis for rapid diagnosis of β-ureidopropionase deficiency in a patient with Dravet syndromeChing-Wan Lam, Chun-Yiu Law, Ka-Fei Leung, et al.
Pediatric Neurology|September 12, 2012
Arginase deficiency with new phenotype and a novel mutation: contemporary summaryJane Pui Ki Tsang, Wai Lun Poon, Ho Ming Luk, et al.
Molecular Carcinogenesis|November 26, 2003
Epigenetic inactivation of TSLC1 gene in nasopharyngeal carcinomaAngela Bik-Yu Hui, Kwok-Wai Lo, Joseph Kwong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 4, 2011
Non-invasive urinary screening for aromatic L-amino acid decarboxylase deficiency in high-prevalence areas: a pilot studyHan-Chih Hencher Lee, Chi-Kong Lai, Kin-Cheong Eric Yau, et al.
Pageof 18

Showing results (121-130 of 179) with videos related to

Sort By:
Pageof 18
Molecular Genetics and Metabolism Reports|December 7, 2023
CYP2U1: An emerging treatable neurometabolic disease with cerebral folate deficiency in 2 Chinese brothersSheila Suet-Na Wong, Liz Yuet-Ping Yuen, Elaine Kan, et al.
Plos Medicine|February 27, 2009
A 21-year-old pregnant woman with hypertension and proteinuriaAndrea Luk, Ronald C W Ma, Ching Wan Lam, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 5, 2023
Allan-Herndon-Dudley syndrome in Hong Kong: Implication for newborn screeningRachel Sze-Wan Yiu, Tsz-Ki Ling, Chun-Hung Ko, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 28, 2009
Diagnosis and spectrum of melamine-related renal disease: plausible mechanism of stone formation in humansChing-Wan Lam, Lawrence Lan, Xiaoyan Che, et al.
Journal of Child Neurology|September 9, 2010
Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiencyWai-Lan Yeung, Virginia C N Wong, Kwok-Yin Chan, et al.
Clinical and Translational Medicine|February 2, 2013
Development and promotion in translational medicine: perspectives from 2012 sino-american symposium on clinical and translational medicineMengjia Qian, Duojiao Wu, Ena Wang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 3, 2014
NMR-based urinalysis for rapid diagnosis of β-ureidopropionase deficiency in a patient with Dravet syndromeChing-Wan Lam, Chun-Yiu Law, Ka-Fei Leung, et al.
Pediatric Neurology|September 12, 2012
Arginase deficiency with new phenotype and a novel mutation: contemporary summaryJane Pui Ki Tsang, Wai Lun Poon, Ho Ming Luk, et al.
Molecular Carcinogenesis|November 26, 2003
Epigenetic inactivation of TSLC1 gene in nasopharyngeal carcinomaAngela Bik-Yu Hui, Kwok-Wai Lo, Joseph Kwong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 4, 2011
Non-invasive urinary screening for aromatic L-amino acid decarboxylase deficiency in high-prevalence areas: a pilot studyHan-Chih Hencher Lee, Chi-Kong Lai, Kin-Cheong Eric Yau, et al.
Pageof 18