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Chuan Tan

Showing results (341-350 of 362) with videos related to

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Genomic Medicine|March 26, 2009
High dose Losartan and ACE gene polymorphism in IgA nephritisKeng-Thye Woo, Choong-Meng Chan, Hui-Lin Choong, et al.
Nephron. Clinical Practice|July 29, 2010
Global evolutionary trend of the prevalence of primary glomerulonephritis over the past three decadesKeng-Thye Woo, Choong-Meng Chan, Yoke Mooi Chin, et al.
Annals of the Academy of Medicine, Singapore|June 21, 2024
Artificial intelligence innovation in healthcare: Relevance of reporting guidelines for clinical translation from bench to bedsideZhen Ling Teo, Ann Kwee, John Cw Lim, et al.
BMC Public Health|March 14, 2024
Extending the diabetic retinopathy screening intervals in Singapore: methodology and preliminary findings of a cohort studyAmudha Aravindhan, Eva K Fenwick, Aurora Wing Dan Chan, et al.
Journal of the American Medical Informatics Association : JAMIA|September 2, 2023
Deep learning algorithms to detect diabetic kidney disease from retinal photographs in multiethnic populations with diabetesBjorn Kaijun Betzler, Evelyn Yi Lyn Chee, Feng He, et al.
Human Molecular Genetics|July 1, 2015
Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiencyChuan Tan, Chloe Shard, Enzo Ranieri, et al.
BMC Infectious Diseases|October 31, 2025
Seroprevalence of COVID-19 neutralizing antibodies among multi-ethnic staff of an Asian primary healthcare institution: insights from point-of-care testing and implications for booster vaccination decisionsPrawira Oka, Huan Jia, Patthara Kongsuphol, et al.
Journal of Clinical Medicine|March 1, 2020
Potential Rapid Diagnostics, Vaccine and Therapeutics for 2019 Novel Coronavirus (2019-nCoV): A Systematic ReviewJunxiong Pang, Min Xian Wang, Ian Yi Han Ang, et al.
Human Molecular Genetics|December 16, 2014
Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorderRaman Kumar, Mark A Corbett, Nicholas J C Smith, et al.
Annals of the Academy of Medicine, Singapore|June 3, 2022
Consensus statement on Singapore integrated 24-hour activity guide for children and adolescentsBenny Kai Guo Loo, Benedict Tan, Michael Yong Hwa Chia, et al.
Pageof 37

Showing results (341-350 of 362) with videos related to

Sort By:
Pageof 37
Genomic Medicine|March 26, 2009
High dose Losartan and ACE gene polymorphism in IgA nephritisKeng-Thye Woo, Choong-Meng Chan, Hui-Lin Choong, et al.
Nephron. Clinical Practice|July 29, 2010
Global evolutionary trend of the prevalence of primary glomerulonephritis over the past three decadesKeng-Thye Woo, Choong-Meng Chan, Yoke Mooi Chin, et al.
Annals of the Academy of Medicine, Singapore|June 21, 2024
Artificial intelligence innovation in healthcare: Relevance of reporting guidelines for clinical translation from bench to bedsideZhen Ling Teo, Ann Kwee, John Cw Lim, et al.
BMC Public Health|March 14, 2024
Extending the diabetic retinopathy screening intervals in Singapore: methodology and preliminary findings of a cohort studyAmudha Aravindhan, Eva K Fenwick, Aurora Wing Dan Chan, et al.
Journal of the American Medical Informatics Association : JAMIA|September 2, 2023
Deep learning algorithms to detect diabetic kidney disease from retinal photographs in multiethnic populations with diabetesBjorn Kaijun Betzler, Evelyn Yi Lyn Chee, Feng He, et al.
Human Molecular Genetics|July 1, 2015
Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiencyChuan Tan, Chloe Shard, Enzo Ranieri, et al.
BMC Infectious Diseases|October 31, 2025
Seroprevalence of COVID-19 neutralizing antibodies among multi-ethnic staff of an Asian primary healthcare institution: insights from point-of-care testing and implications for booster vaccination decisionsPrawira Oka, Huan Jia, Patthara Kongsuphol, et al.
Journal of Clinical Medicine|March 1, 2020
Potential Rapid Diagnostics, Vaccine and Therapeutics for 2019 Novel Coronavirus (2019-nCoV): A Systematic ReviewJunxiong Pang, Min Xian Wang, Ian Yi Han Ang, et al.
Human Molecular Genetics|December 16, 2014
Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorderRaman Kumar, Mark A Corbett, Nicholas J C Smith, et al.
Annals of the Academy of Medicine, Singapore|June 3, 2022
Consensus statement on Singapore integrated 24-hour activity guide for children and adolescentsBenny Kai Guo Loo, Benedict Tan, Michael Yong Hwa Chia, et al.
Pageof 37