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Ching-Wan Lam

Showing results (91-100 of 179) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|October 21, 2015
Clinical whole-exome sequencing reveals a novel missense pathogenic variant of GNAO1 in a patient with infantile-onset epilepsyChun-Yiu Law, Sharon Tzu-Lun Chang, Sun Young Cho, et al.
Pathology|October 27, 2021
Nuclear magnetic resonance spectroscopy-based urinalysis for a young girl with extreme hypoglycaemiaChun-Yiu Law, Anne Mei-Kwun Kwok, Tsz-Ki Ling, et al.
Chinese Medical Journal|July 2, 2005
Early-onset primary torsional dystonia in a 4-generation Chinese family with a mutation in the DYT1 geneWai Lan Yeung, Ching Wan Lam, Wai Tsoi Cheng, et al.
Human Mutation|August 31, 2002
Genotype-phenotype studies of six novel LPL mutations in Chinese patients with hypertriglyceridemiaLisa Y S Chan, Ching-Wan Lam, Ying-Tat Mak, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 25, 2014
Dystroglycanopathy with two novel POMT1 mutations in a Chinese boy with developmental delay and muscular dystrophyYeow Kuan Chong, Louis Che Kwan Ma, Kit Lin Lo, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 15, 2015
Novel POLG mutation in a patient with sensory ataxia, neuropathy, ophthalmoparesis and strokeChing-Wan Lam, Chun-Yiu Law, Wai-Kwan Siu, et al.
Leukemia Research|May 27, 2006
Solid tumors subsequent to arsenic trioxide treatment for acute promyelocytic leukemiaWing-Yan Au, Cyrus R Kumana, Ching-Wan Lam, et al.
Experimental Biology and Medicine (Maywood, N.J.)|April 25, 2015
Laboratory diagnosis of melioidosis: past, present and futureSusanna K P Lau, Siddharth Sridhar, Chi-Chun Ho, et al.
Sleep & Breathing = Schlaf & Atmung|August 12, 2009
Maternally inherited Leigh syndrome: an unusual cause of infantile apneaChristy Shuk-kuen Chau, Ka-li Kwok, Daniel K Ng, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 7, 2020
Centrosome-associated CDC25B is a novel disease-causing gene for a syndrome with cataracts, dilated cardiomyopathy, and multiple endocrinopathiesChing-Wan Lam, Nai-Chung Fong, Tina Yee-Ching Chan, et al.
Pageof 18

Showing results (91-100 of 179) with videos related to

Sort By:
Pageof 18
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 21, 2015
Clinical whole-exome sequencing reveals a novel missense pathogenic variant of GNAO1 in a patient with infantile-onset epilepsyChun-Yiu Law, Sharon Tzu-Lun Chang, Sun Young Cho, et al.
Pathology|October 27, 2021
Nuclear magnetic resonance spectroscopy-based urinalysis for a young girl with extreme hypoglycaemiaChun-Yiu Law, Anne Mei-Kwun Kwok, Tsz-Ki Ling, et al.
Chinese Medical Journal|July 2, 2005
Early-onset primary torsional dystonia in a 4-generation Chinese family with a mutation in the DYT1 geneWai Lan Yeung, Ching Wan Lam, Wai Tsoi Cheng, et al.
Human Mutation|August 31, 2002
Genotype-phenotype studies of six novel LPL mutations in Chinese patients with hypertriglyceridemiaLisa Y S Chan, Ching-Wan Lam, Ying-Tat Mak, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 25, 2014
Dystroglycanopathy with two novel POMT1 mutations in a Chinese boy with developmental delay and muscular dystrophyYeow Kuan Chong, Louis Che Kwan Ma, Kit Lin Lo, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 15, 2015
Novel POLG mutation in a patient with sensory ataxia, neuropathy, ophthalmoparesis and strokeChing-Wan Lam, Chun-Yiu Law, Wai-Kwan Siu, et al.
Leukemia Research|May 27, 2006
Solid tumors subsequent to arsenic trioxide treatment for acute promyelocytic leukemiaWing-Yan Au, Cyrus R Kumana, Ching-Wan Lam, et al.
Experimental Biology and Medicine (Maywood, N.J.)|April 25, 2015
Laboratory diagnosis of melioidosis: past, present and futureSusanna K P Lau, Siddharth Sridhar, Chi-Chun Ho, et al.
Sleep & Breathing = Schlaf & Atmung|August 12, 2009
Maternally inherited Leigh syndrome: an unusual cause of infantile apneaChristy Shuk-kuen Chau, Ka-li Kwok, Daniel K Ng, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 7, 2020
Centrosome-associated CDC25B is a novel disease-causing gene for a syndrome with cataracts, dilated cardiomyopathy, and multiple endocrinopathiesChing-Wan Lam, Nai-Chung Fong, Tina Yee-Ching Chan, et al.
Pageof 18