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Analytical Biochemistry|November 30, 2010
Detection of hemi/homozygotes through heteroduplex formation in high-resolution melting analysisJinting Cheng, Onn-Siong Yim, Poh-Sim Low, et al.Journal of Clinical Medicine|May 4, 2026
Thrombosis in Neuromuscular Medicine: Current Evidence, Unmet Needs, and Future DirectionsZhi Xuan Quak, Furene Wang, Stacey K H Tay, et al.Archives of Neurology|December 15, 2004
Studies of COX16, COX19, and PET191 in human cytochrome-c oxidase deficiencyStacey K H Tay, Claudia Nesti, Michelangelo Mancuso, et al.Journal of Child Neurology|March 30, 2005
Clinical and genetic features in two families with MELAS and the T3271C mutation in mitochondrial DNAStacey K H Tay, Sara Shanske, Carol Crowe, et al.Annals of the Academy of Medicine, Singapore|November 24, 1999
Magnetic resonance imaging of brain metastases: magnetisation transfer or triple dose gadolinium?C H Thng, K H Tay, L L Chan, et al.Singapore Medical Journal|November 29, 2007
Management of pyogenic liver abscesses - percutaneous or open drainage?Y F A Chung, Y M Tan, H F Lui, et al.Molecular Genetics and Metabolism|May 30, 2007
Unusually mild phenotype of AADC deficiency in 2 siblingsS K H Tay, K S Poh, K Hyland, et al.Circulation Journal : Official Journal of the Japanese Circulation Society|August 29, 2006
Displacement of the beating heart induces an immediate and sustained increase in myocardial reactive oxygen speciesZakaria A Almsherqi, Craig S McLachlan, Iouri Kostetski, et al.Annals of the Academy of Medicine, Singapore|February 24, 2005
Uterine artery embolisation for symptomatic fibroids in a tertiary hospital in SingaporeP C Mohan, B S Tan, B H Kwek, et al.Journal of Child Neurology|October 18, 2005
Unusual clinical presentations in four cases of Leigh disease, cytochrome C oxidase deficiency, and SURF1 gene mutationsStacey K H Tay, Sabrina Sacconi, H Ohran Akman, et al.Pageof 9