Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Chloe Mak"'
Autor:
Tong Liu, Gary Tse, Ian Chi Kei Wong, Qingpeng Zhang, Jiandong Zhou, Sharen Lee, Ngai Shing Mok, Chloe Mak, Kamalan Jeevaratnam, Wing Tak Wong
Publikováno v:
Open Heart, Vol 8, Iss 2 (2021)
Introduction Long QT syndrome (LQTS) is a less prevalent cardiac ion channelopathy than Brugada syndrome in Asia. The present study compared the outcomes between paediatric/young and adult LQTS patients.Methods This was a population-based retrospecti
Externí odkaz:
https://doaj.org/article/ba5de65b8e264bc48c47958531568aec
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
Introduction: Brugada syndrome (BrS) is a cardiac ion channelopathy with a higher prevalence in Asia compared to the Western populations. The present study compared the differences in clinical and electrocardiographic (ECG) presentation between paedi
Externí odkaz:
https://doaj.org/article/71233981b4aa4a78be897fcd608138fb
Autor:
Gary Tse, Sharen Lee, Jiandong Zhou, Tong Liu, Ian Chi Kei Wong, Chloe Mak, Ngai Shing Mok, Kamalan Jeevaratnam, Qingpeng Zhang, Shuk Han Cheng, Wing Tak Wong
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
Introduction: Congenital long QT syndrome (LQTS) is a cardiac ion channelopathy that predisposes affected individuals to spontaneous ventricular tachycardia/fibrillation (VT/VF) and sudden cardiac death (SCD). The main aims of the study were to: (1)
Externí odkaz:
https://doaj.org/article/3ee884a754f443d7ba8815f7623d8322
Autor:
Ka Hou Christien Li, Tong Liu, Gary Tse, Ian Chi Kei Wong, Qingpeng Zhang, Jiandong Zhou, Sharen Lee, Keith Sai Kit Leung, Ishan Lakhani, Ngai Shing Mok, Chloe Mak
Publikováno v:
Open Heart, Vol 8, Iss 1 (2021)
Objectives Brugada syndrome (BrS) is an ion channelopathy that predisposes affected patients to spontaneous ventricular tachycardia/fibrillation (VT/VF) and sudden cardiac death. The aim of this study is to examine the predictive factors of spontaneo
Externí odkaz:
https://doaj.org/article/bbc71df1919c4f108fcf81cc74e9794a
Autor:
Gary Tse, Sharen Lee, Tong Liu, Ho Chuen Yuen, Ian Chi Kei Wong, Chloe Mak, Ngai Shing Mok, Wing Tak Wong
Publikováno v:
Frontiers in Physiology, Vol 11 (2020)
BackgroundThe aim of this study is to report on the genetic composition of Brugada syndrome (BrS) patients undergoing genetic testing in Hong Kong.MethodsPatients with suspected BrS who presented to the Hospital Authority of Hong Kong between 1997 an
Externí odkaz:
https://doaj.org/article/03903d30b82846f0be0510d0a47ef760
Autor:
Tse, Gary, Sharen Lee, Tong Liu, Ho Chuen Yuen, Ian Chi Kei Wong, Chloe Mak, Ngai Shing Mok, Wing Tak Wong
Publikováno v:
Frontiers in Physiology; 2024, p1-6, 6p
Autor:
Jakob Zierk, Sharon M. Geaghan, Tim Lang, Chloe Mak, Tze Ping Loh, Ronda F. Greaves, Klaus P. Kohse, Ioannis Papassotiriou
Publikováno v:
Journal of Laboratory Medicine, Vol 45, Iss 6, Pp 245-248 (2021)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ca873cd6f063fab4082a273c9fe8fdd
https://doaj.org/article/f29b6b8963714ae19e24c214b0d1415c
https://doaj.org/article/f29b6b8963714ae19e24c214b0d1415c
Autor:
Matthew Chun Wing Yeung, Kwok Yeung Tsang, Chloe Mak, Toby Chun Hei Chan, Tsz Ki Wong, Wan Ting Lau
Publikováno v:
Journal of Laboratory Medicine, Vol 45, Iss 6, Pp 267-274 (2021)
Objectives Next generation sequencing (NGS) technology has allowed cost-effective massive parallel DNA sequencing. To evaluate the utility of NGS for newborn screening (NBS) of inborn errors of metabolism (IEM), a custom panel was designed to target
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88da3cc2b7c826ae95a91c2b2df11907
https://doi.org/10.1515/labmed-2021-0115
https://doi.org/10.1515/labmed-2021-0115
Autor:
Yeow-Kuan Chong, Lai-Ka Lee, Tsz-ki Ling, Han-Chih Hencher Lee, Chun-Hung Ko, Candace Yim Chan, Ching-Wan Lam, Chloe Mak, Nike Kwai-Cheung Lau, Cheuk-Wing Fung, Sheila Suet-Na Wong, Sidney Tam, Chun-yiu Law, K M Cheung, Chi-Kong Lai, Kin-Cheong Eric Yau, Albert Y W Chan, Ka-chung Wong
Publikováno v:
Clinica Chimica Acta. 521:40-44
Background Aromatic L-amino acid decarboxylase deficiency is a rare neurometabolic disease due to impaired decarboxylation of neurotransmitter precursors to its active form. Case: We retrospectively reviewed 8 cases from 2008 to 2019 with cerebrospin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc11642968b04a807262772013c3e60e
https://doi.org/10.1016/j.cca.2021.06.025
https://doi.org/10.1016/j.cca.2021.06.025
Autor:
Qingpeng Zhang, Tong Liu, Guoqiang Li, Chloe Mak, K. H. C. Lee, Gary Tse, I. Lakhani, Ian C. K. Wong, Wing Tak Wong, Ngai Shing Mok, Jiandong Zhou, S. Lee, Keith Sai Kit Leung
BackgroundArrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a hereditary disease characterized by fibrofatty infiltration of the right ventricular myocardium that predisposes affected patients to malignant ventricular arrhythmias,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f1914bf35e4977a10daa9b02672a892
https://doi.org/10.1101/2021.11.17.21266304
https://doi.org/10.1101/2021.11.17.21266304
