Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Felix Chi-Kin Wong"'
Autor:
Ka Wang Cheung, MD, Tiffany Sin-Tung Au, BSc, Chi-Ho Lee, MD, Vivian Wai Yan Ng, MBBS, Felix Chi-Kin Wong, MBBS, Wing-Sun Chow, MBBS, Pui Wah Hui, MD, Mimi Tin Yan Seto, MBBS
Publikováno v:
AJOG Global Reports, Vol 4, Iss 1, Pp 100315- (2024)
BACKGROUND: Unrecognized diabetes mellitus during pregnancy could pose serious maternal and neonatal complications. A hemoglobin A1c level of ≥6.5% was used to diagnose both diabetes mellitus in nonpregnant individuals and diabetes in pregnancy. As
Externí odkaz:
https://doaj.org/article/2b95e69ecf1840b4a3eaa88fde96507a
Autor:
Jenny Yeuk-Ki Cheng, Felix Chi-Kin Wong, Edith Wing-Kar Chow, Wendy Wan-Hang Lau, Kitty Kit-Ting Cheung, Timothy Hua-Tse Cheng, Teresa Kam-Chi Tsui, Alan Shek-Lun Chan, Clara Wai-Shan Lo, Chung-Shun Ho
Publikováno v:
Clinical Chemistry and Laboratory Medicine (CCLM). 60:1640-1647
Objectives The renin-angiotensin-aldosterone system (RAAS) regulates blood pressure. Plasma renin activities (PRA) and plasma aldosterone concentrations (PAC) are biomarkers related to RAAS. Liquid chromatography-tandem mass spectrometry (LC-MS/MS)-b
Autor:
Sau Wing Yim, Tina Yee Ching Chan, Kiran M. Belaramani, Sze Shun Man, Felix Chi Kin Wong, Sammy Pak Lam Chen, Hencher Han Chih Lee, Chloe Miu Mak, Chor Kwan Ching
Publikováno v:
F1000Research, Vol 8 (2019)
Recurrent rhabdomyolysis is frequently ascribed to fatty acid ß-oxidation defects, mitochondrial respiratory chain disorders and glycogen storage-related diseases. In recent years, autosomal recessive LPIN1 mutations have been identified as a prevai
Externí odkaz:
https://doaj.org/article/00ac1c515c5148708a69f2ac99350c53
Autor:
Felix Chi Kin Wong, Wai Sheung Wong, Jeffrey Sung Shing Kwok, Teresa Kam Chi Tsui, Kam Piu Lau, Michael Ho Ming Chan, Yuet Ping Yuen
Publikováno v:
F1000Research, Vol 8 (2019)
Familial hypocalciuric hypercalcaemia (FHH) is a genetic disorder of altered calcium homeostasis. Mutations in the CASR, GNA11 and AP2S1 genes have been reported to cause FHH. We report a Hong Kong Chinese kindred with FHH type 3 (FHH3) caused by mut
Externí odkaz:
https://doaj.org/article/5a45dbff301b4019916e788f89fe215f
Publikováno v:
Pathology. 54:S67
Autor:
Mei Tik Leung, Ling Yin Hung, Diana Siao Cheng Han, Felix Chi Kin Wong, Shreenidhi Ranganatha Subramaniam
Publikováno v:
Clinical Chemistry. 66:627-628