Zobrazeno 1 - 10
of 1 814
pro vyhledávání: '"So Lun Lee"'
Autor:
Jeffrey Fong Ting Chau, Mullin Ho Chung Yu, Martin Man Chun Chui, Cyrus Chun Wing Yeung, Aaron Wing Cheung Kwok, Xuehan Zhuang, Ryan Lee, Jasmine Lee Fong Fung, Mianne Lee, Christopher Chun Yu Mak, Nicole Ying Ting Ng, Claudia Ching Yan Chung, Marcus Chun Yin Chan, Mandy Ho Yin Tsang, Joshua Chun Ki Chan, Kelvin Yuen Kwong Chan, Anita Sik Yau Kan, Patrick Ho Yu Chung, Wanling Yang, So Lun Lee, Godfrey Chi Fung Chan, Paul Kwong Hang Tam, Yu Lung Lau, Kit San Yeung, Brian Hon Yin Chung, Clara Sze Man Tang
Publikováno v:
npj Genomic Medicine, Vol 7, Iss 1, Pp 1-9 (2022)
Abstract Traditional carrier screening has been utilized for the detection of carriers of genetic disorders. Since a comprehensive assessment of the carrier frequencies of recessive conditions in the Southern Chinese population is not yet available,
Externí odkaz:
https://doaj.org/article/a4439854ca474791ac85c6eeb89fbddb
Autor:
Claudia C. Y. Chung, Jasmine L. F. Fung, Adrian C. Y. Lui, Marcus C. Y. Chan, Yvette N. C. Ng, Wilfred H. S. Wong, So Lun Lee, Martin Knapp, Brian H. Y. Chung
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract The measurement of costs is fundamental in healthcare decision-making, but it is often challenging. In particular, standardised methods have not been developed in the rare genetic disease population. A reliable and valid tool is critical for
Externí odkaz:
https://doaj.org/article/4efed92bdf984270ad8f041bdb5d02a0
Autor:
Chi Hang Wong, Jaime Rosa Duque, Joshua Sung Chih Wong, Chi-man Victor Chan, Cheuk San Ivan Lam, Yu Ming Fu, Kai-Ning Cheong, Gilbert T. Chua, Pamela P. Lee, Patrick Ip, Marco Hok Kung Ho, Ian Chi Kei Wong, Godfrey Chi Fung Chan, Wing Hang Leung, So Lun Lee, Kwok Piu Lee, Chi Chiu Shek, Ming Sum Rosanna Wong, Mabel Siu Chun Wong, Yu-Lung Lau, Mike Yat-wah Kwan
Publikováno v:
International Journal of Infectious Diseases, Vol 111, Iss , Pp 288-294 (2021)
Objectives: Meningitis in neonates and young infants leads to significant morbidity and mortality worldwide. This study aimed to investigate pathogens, antibiotic resistance and secular change of incidence in Hong Kong. Methods: A retrospective searc
Externí odkaz:
https://doaj.org/article/ac4344219f0b410d823262525327dc9b
Autor:
Mullin Ho Chung Yu, Marcus Chun Yin Chan, Claudia Ching Yan Chung, Andrew Wang Tat Li, Chara Yin Wa Yip, Christopher Chun Yu Mak, Jeffrey Fong Ting Chau, Mianne Lee, Jasmine Lee Fong Fung, Mandy Ho Yin Tsang, Joshua Chun Ki Chan, Wilfred Hing Sang Wong, Jing Yang, William Chun Ming Chui, Patrick Ho Yu Chung, Wanling Yang, So Lun Lee, Godfrey Chi Fung Chan, Paul Kwong Hang Tam, Yu Lung Lau, Clara Sze Man Tang, Kit San Yeung, Brian Hon Yin Chung
Publikováno v:
PLoS Genetics, Vol 17, Iss 2, p e1009323 (2021)
Preemptive pharmacogenetic testing has the potential to improve drug dosing by providing point-of-care patient genotype information. Nonetheless, its implementation in the Chinese population is limited by the lack of population-wide data. In this stu
Externí odkaz:
https://doaj.org/article/17bc0de37ec248a2bc84c547426580ef
Autor:
Claudia C.Y. Chung, Gordon K.C. Leung, Christopher C.Y. Mak, Jasmine L.F. Fung, Mianne Lee, Steven L.C. Pei, Mullin H.C. Yu, Vivian C.C. Hui, Joshua C.K. Chan, Jeffrey F.T. Chau, Marcus C.Y. Chan, Mandy H.Y. Tsang, Wilfred H.S. Wong, Joanna Y.L. Tung, Kin Shing Lun, Yiu Ki Ng, Cheuk Wing Fung, Mabel S.C. Wong, Rosanna M.S. Wong, Yu Lung Lau, Godfrey C.F. Chan, So Lun Lee, Kit San Yeung, Brian H.Y. Chung
Publikováno v:
The Lancet Regional Health. Western Pacific, Vol 1, Iss , Pp 100001- (2020)
Background: Rapid whole-exome sequencing (rWES) offers the potential for early diagnosis-predicated precision medicine. Previous evidence focused predominantly on infants from the intensive care unit (ICU). This study sought to examine the diagnostic
Externí odkaz:
https://doaj.org/article/e398ebf6ac4d424a93584d7da343cb7a
Autor:
Yuet Yee Chee FHKAM, Rosanna Ming Sum Wong FHKAM, Mabel Siu Chun Wong FHKAM, Winnie Wan Yee Tso FHKAM, Wilfred Hing Sang Wong MMedSc, PhD, So Lun Lee FHKAM
Publikováno v:
Global Pediatric Health, Vol 7 (2020)
Introduction . We retrospectively reviewed a cohort of extremely low-birth-weight (ELBW) babies born at Queen Mary Hospital and explored if there is any time trend in survival and short-term neurodevelopmental outcomes. Methods . We included ELBW inf
Externí odkaz:
https://doaj.org/article/f0cb465c58ed4b019116664feffe18f2
Autor:
Annie Ting Gee Chiu, Claudia Ching Yan Chung, Wilfred Hing Sang Wong, So Lun Lee, Brian Hon Yin Chung
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-8 (2018)
Abstract Background The burden of rare diseases is important for healthcare planning but difficult to estimate. This has been facilitated by the development of ORPHAcodes, a comprehensive classification and coding system for rare diseases developed b
Externí odkaz:
https://doaj.org/article/17ae8a9a46544d9eba7635a1146b4d36
Autor:
Kit San Yeung, Winnie Wan Yee Tso, Janice Jing Kun Ip, Christopher Chun Yu Mak, Gordon Ka Chun Leung, Mandy Ho Yin Tsang, Dingge Ying, Steven Lim Cho Pei, So Lun Lee, Wanling Yang, Brian Hon-Yin Chung
Publikováno v:
Molecular Autism, Vol 8, Iss 1, Pp 1-11 (2017)
Abstract Background Macrocephaly, which is defined as a head circumference greater than or equal to + 2 standard deviations, is a feature commonly observed in children with developmental delay and/or autism spectrum disorder. Although PTEN is a well-
Externí odkaz:
https://doaj.org/article/9b94f5a06273458588cf48e2ab2e0cf9
Autor:
Annisa Shui Lam Mak, Annie Ting Gee Chiu, Gordon Ka Chun Leung, Christopher Chun Yu Mak, Yoyo Wing Yiu Chu, Gary Tsz Kin Mok, Wing Fai Tang, Kelvin Yuen Kwong Chan, Mary Hoi Yin Tang, Elizabeth Tak-Kwong Lau Yim, Kin Wai So, Victoria Qinchen Tao, Cheuk Wing Fung, Virginia Chun Nei Wong, Mohammed Uddin, So Lun Lee, Christian R. Marshall, Stephen W. Scherer, Anita Sik Yau Kan, Brian Hon Yin Chung
Publikováno v:
Molecular Autism, Vol 8, Iss 1, Pp 1-12 (2017)
Abstract Background Array comparative genomic hybridization (aCGH) is recommended as a first-tier genetic test for children with autism spectrum disorder (ASD). However, interpretation of results can often be challenging partly due to the fact that c
Externí odkaz:
https://doaj.org/article/f4d95ed70644412987ce07feaa2f58c6
Autor:
Pei-Chien Tsai, Chung-Feng Huang, Ming-Lun Yeh, Meng-Hsuan Hsieh, Hsing-Tao Kuo, Chao-Hung Hung, Kuo-Chih Tseng, Hsueh-Chou Lai, Cheng-Yuan Peng, Jing-Houng Wang, Jyh-Jou Chen, Pei-Lun Lee, Rong-Nan Chien, Chi-Chieh Yang, Gin-Ho Lo, Jia-Horng Kao, Chun-Jen Liu, Chen-Hua Liu, Sheng-Lei Yan, Chun-Yen Lin, Wei-Wen Su, Cheng-Hsin Chu, Chih-Jen Chen, Shui-Yi Tung, Chi‐Ming Tai, Chih-Wen Lin, Ching-Chu Lo, Pin-Nan Cheng, Yen-Cheng Chiu, Chia-Chi Wang, Jin-Shiung Cheng, Wei-Lun Tsai, Han-Chieh Lin, Yi-Hsiang Huang, Chi-Yi Chen, Jee-Fu Huang, Chia-Yen Dai, Wan-Long Chung, Ming-Jong Bair, Ming-Lung Yu, T-COACH Study Group
Publikováno v:
Clinical and Molecular Hepatology, Vol 30, Iss 3, Pp 468-486 (2024)
Background/Aims Chronic hepatitis C (CHC) patients who failed antiviral therapy are at increased risk for hepatocellular carcinoma (HCC). This study assessed the potential role of metformin and statins, medications for diabetes mellitus (DM) and hype
Externí odkaz:
https://doaj.org/article/c4b167d9986a4d858ee7c5d56f112a9c