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Ching-Wan Lam

Showing results (101-110 of 179) with videos related to

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Chemical Communications (Cambridge, England)|February 16, 2019
Plasmonic gold nanoparticles as multifaceted probe for tissue imagingYu-Hong Cheng, Toby Siu-Chung Tam, Siu-Leung Chau, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|August 1, 2012
Molecular diagnosis for a fatal case of very long-chain acyl-CoA dehydrogenase deficiency in Hong Kong Chinese with a novel mutation: a preventable death by newborn screeningWai-Kwan Siu, Chloe Miu Mak, Sylvia Luen-Yee Siu, et al.
Plos Neglected Tropical Diseases|October 25, 2012
First discovery of two polyketide synthase genes for mitorubrinic acid and mitorubrinol yellow pigment biosynthesis and implications in virulence of Penicillium marneffeiPatrick C Y Woo, Ching-Wan Lam, Emily W T Tam, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 10, 2014
NMR-based metabolomic urinalysis: a rapid screening test for urinary tract infectionChing-Wan Lam, Chun-Yiu Law, Kelvin Kai-Wang To, et al.
Human Mutation|March 26, 2003
Pathogenic mutations of the lipoprotein lipase gene in Chinese patients with hypertriglyceridemic type 2 diabetesTao Yang, Chi-Pui Pang, Man-Wo Tsang, et al.
Clinical Toxicology (Philadelphia, Pa.)|May 28, 2021
Serum ceruloplasmin monitoring in a case of silver intoxication due to intravenous silver infusionChun-Yiu Law, Siu-Chung Leung, Florence Loong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 2, 2008
A novel mutation of SLC22A12 gene causing primary renal hypouricemia in a patient with metabolic syndromeChing-Wan Lam, Alice P S Kong, Teresa K C Tsui, et al.
Analytical Chemistry|April 4, 2009
Analysis of melamine cyanurate in urine using matrix-assisted laser desorption/ionization mass spectrometryHo-Wai Tang, Kwan-Ming Ng, Stephen Sin-Yin Chui, et al.
Chinese Medical Journal|July 23, 2002
Novel mitochondrial 16S rRNA mutation, 3200T-->C, associated with adult-onset type 2 diabetesTao Yang, Ching-Wan Lam, Man-Wo Tsang, et al.
Pediatric Nephrology (Berlin, Germany)|September 3, 2024
Familial thrombotic microangiopathy in a child with coenzyme Q10 deficiency-associated glomerulopathyKyle Ying-Kit Lin, Ching-Wan Lam, Eugene Yu-Hin Chan, et al.
Pageof 18

Showing results (101-110 of 179) with videos related to

Sort By:
Pageof 18
Chemical Communications (Cambridge, England)|February 16, 2019
Plasmonic gold nanoparticles as multifaceted probe for tissue imagingYu-Hong Cheng, Toby Siu-Chung Tam, Siu-Leung Chau, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|August 1, 2012
Molecular diagnosis for a fatal case of very long-chain acyl-CoA dehydrogenase deficiency in Hong Kong Chinese with a novel mutation: a preventable death by newborn screeningWai-Kwan Siu, Chloe Miu Mak, Sylvia Luen-Yee Siu, et al.
Plos Neglected Tropical Diseases|October 25, 2012
First discovery of two polyketide synthase genes for mitorubrinic acid and mitorubrinol yellow pigment biosynthesis and implications in virulence of Penicillium marneffeiPatrick C Y Woo, Ching-Wan Lam, Emily W T Tam, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 10, 2014
NMR-based metabolomic urinalysis: a rapid screening test for urinary tract infectionChing-Wan Lam, Chun-Yiu Law, Kelvin Kai-Wang To, et al.
Human Mutation|March 26, 2003
Pathogenic mutations of the lipoprotein lipase gene in Chinese patients with hypertriglyceridemic type 2 diabetesTao Yang, Chi-Pui Pang, Man-Wo Tsang, et al.
Clinical Toxicology (Philadelphia, Pa.)|May 28, 2021
Serum ceruloplasmin monitoring in a case of silver intoxication due to intravenous silver infusionChun-Yiu Law, Siu-Chung Leung, Florence Loong, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 2, 2008
A novel mutation of SLC22A12 gene causing primary renal hypouricemia in a patient with metabolic syndromeChing-Wan Lam, Alice P S Kong, Teresa K C Tsui, et al.
Analytical Chemistry|April 4, 2009
Analysis of melamine cyanurate in urine using matrix-assisted laser desorption/ionization mass spectrometryHo-Wai Tang, Kwan-Ming Ng, Stephen Sin-Yin Chui, et al.
Chinese Medical Journal|July 23, 2002
Novel mitochondrial 16S rRNA mutation, 3200T-->C, associated with adult-onset type 2 diabetesTao Yang, Ching-Wan Lam, Man-Wo Tsang, et al.
Pediatric Nephrology (Berlin, Germany)|September 3, 2024
Familial thrombotic microangiopathy in a child with coenzyme Q10 deficiency-associated glomerulopathyKyle Ying-Kit Lin, Ching-Wan Lam, Eugene Yu-Hin Chan, et al.
Pageof 18