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Journal of Pediatric Endocrinology & Metabolism : JPEM
|
November 5, 2003
Steroid 5alpha-reductase 2 deficiency in two generations of a non-consanguineous Chinese family
Ching-Yin Lee, Ching-Wan Lam, Chi-Chung Shek
Neurology
|
November 9, 2005
Stiff child syndrome with mutation of DYT1 gene
Virginia C N Wong, Ching-Wan Lam, Cheuk Wing Fung
Canadian Journal of Gastroenterology & Hepatology
|
November 30, 2013
Follow-up of participants in the Canadian Association of Gastroenterology Scholars' Program, 2006 to 2012
Mindy Ching Wan Lam, Michael Sl Sey, Jamie Gregor, et al.
Pathology
|
December 23, 2009
Genotype-confirmed alanine aminotransferase deficiency in a Chinese patient with acute liver failure: a potential diagnostic pitfall
Chloe Miu Mak, Bonnie Mei-Wah Fong, Ching-Wan Lam, et al.
Journal of Paediatrics and Child Health
|
October 22, 2008
Hyperinsulinism and hyperammonaemia syndrome due to a novel missense mutation in the allosteric domain of the glutamate dehydrogenase 1 gene
Kar-Ki Chik, Chun-Wing Chan, Ching-Wan Lam, et al.
Rapid Communications in Mass Spectrometry : RCM
|
December 17, 2011
Organochlorine isotopic pattern-enhanced detection and quantification of triclosan and its metabolites in human serum by ultra-high-performance liquid chromatography/quadrupole time-of-flight/mass spectrometry
Jian-lin Wu, Ka-Fai Leung, Sui-Fan Tong, et al.
Journal of Cardiovascular Electrophysiology
|
January 13, 2006
Ketoconazole induced torsades de pointes without concomitant use of QT interval-prolonging drug
Ngai-Shing Mok, Ying-Keung Lo, Ping-Tim Tsui, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 24, 2013
X-linked glycogen storage disease IXa manifested in a female carrier due to skewed X chromosome inactivation
Sun Young Cho, Ching-wan Lam, Sui-Fan Tong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 2, 2016
Novel large deletion in AVPR2 gene causing copy number variation in a patient with X-linked nephrogenic diabetes insipidus
Sun Young Cho, Chun Yiu Law, Kwok Leung Ng, et al.
European Journal of Human Genetics : EJHG
|
December 15, 2016
Limb girdle myasthenia with digenic RAPSN and a novel disease gene AK9 mutations
Ching-Wan Lam, Ka-Sing Wong, Ho-Wan Leung, et al.
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of 18
Search research articles
Search
Showing results (21-30 of 178) with videos related to
Sort By:
Page
of 18
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
November 5, 2003
Steroid 5alpha-reductase 2 deficiency in two generations of a non-consanguineous Chinese family
Ching-Yin Lee, Ching-Wan Lam, Chi-Chung Shek
Neurology
|
November 9, 2005
Stiff child syndrome with mutation of DYT1 gene
Virginia C N Wong, Ching-Wan Lam, Cheuk Wing Fung
Canadian Journal of Gastroenterology & Hepatology
|
November 30, 2013
Follow-up of participants in the Canadian Association of Gastroenterology Scholars' Program, 2006 to 2012
Mindy Ching Wan Lam, Michael Sl Sey, Jamie Gregor, et al.
Pathology
|
December 23, 2009
Genotype-confirmed alanine aminotransferase deficiency in a Chinese patient with acute liver failure: a potential diagnostic pitfall
Chloe Miu Mak, Bonnie Mei-Wah Fong, Ching-Wan Lam, et al.
Journal of Paediatrics and Child Health
|
October 22, 2008
Hyperinsulinism and hyperammonaemia syndrome due to a novel missense mutation in the allosteric domain of the glutamate dehydrogenase 1 gene
Kar-Ki Chik, Chun-Wing Chan, Ching-Wan Lam, et al.
Rapid Communications in Mass Spectrometry : RCM
|
December 17, 2011
Organochlorine isotopic pattern-enhanced detection and quantification of triclosan and its metabolites in human serum by ultra-high-performance liquid chromatography/quadrupole time-of-flight/mass spectrometry
Jian-lin Wu, Ka-Fai Leung, Sui-Fan Tong, et al.
Journal of Cardiovascular Electrophysiology
|
January 13, 2006
Ketoconazole induced torsades de pointes without concomitant use of QT interval-prolonging drug
Ngai-Shing Mok, Ying-Keung Lo, Ping-Tim Tsui, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 24, 2013
X-linked glycogen storage disease IXa manifested in a female carrier due to skewed X chromosome inactivation
Sun Young Cho, Ching-wan Lam, Sui-Fan Tong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 2, 2016
Novel large deletion in AVPR2 gene causing copy number variation in a patient with X-linked nephrogenic diabetes insipidus
Sun Young Cho, Chun Yiu Law, Kwok Leung Ng, et al.
European Journal of Human Genetics : EJHG
|
December 15, 2016
Limb girdle myasthenia with digenic RAPSN and a novel disease gene AK9 mutations
Ching-Wan Lam, Ka-Sing Wong, Ho-Wan Leung, et al.
Page
of 18