Zobrazeno 1 - 10
of 15
pro vyhledávání: '"David K H Chan"'
Autor:
Chandu Sadasivan, Josie T Y Chow, Bun Sheng, David K H Chan, Yiting Fan, Paul C L Choi, Jeffrey K T Wong, Mabel M B Tong, Tsz-Ngai Chan, Erik Fung, Kevin K H Kam, Joseph Y S Chan, Wai-Kin Chi, D Ian Paterson, Manohara Senaratne, Neil Brass, Gavin Y Oudit, Alex P W Lee
Publikováno v:
PLoS ONE, Vol 15, Iss 9, p e0239675 (2020)
Fabry Disease (FD) is a systemic disorder that can result in cardiovascular, renal, and neurovascular disease leading to reduced life expectancy. FD should be considered in the differential of all patients with unexplained left ventricular hypertroph
Externí odkaz:
https://doaj.org/article/d710dc75f1be46ac9b0429cca5766eb1
Autor:
Bun Sheng, Josie T. Y. Chow, David K. H. Chan, Erik Fung, Alex Pui-Wai Lee, Paul Cheung-Lung Choi, Tsz-Ngai Chan, Joseph Y.S. Chan, Mabel M P Tong, Kevin Ka-Ho Kam, Wai-Kin Chi, Yiting Fan, Jeffery K T Wong
Publikováno v:
Journal of Clinical Medicine
Volume 10
Issue 10
Journal of Clinical Medicine, Vol 10, Iss 2160, p 2160 (2021)
Volume 10
Issue 10
Journal of Clinical Medicine, Vol 10, Iss 2160, p 2160 (2021)
Left ventricular hypertrophy (LVH) caused by cardiac variant Fabry disease (FD) is typically late-onset and may mimic LVH caused by abnormal loading conditions. We aimed to determine the prevalence of FD in a non-selective patient population of every
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f0844449b7d7e96b77d582ef9461455
Autor:
Jeffrey Ka-Tat Wong, Kevin Ka-Ho Kam, David K. H. Chan, D. Ian Paterson, Joseph Y.S. Chan, Yiting Fan, Wai-Kin Chi, Alex Pui-Wai Lee, Mabel M. B. Tong, Bun Sheng, Erik Fung, Chandu Sadasivan, Gavin Y. Oudit, Neil Brass, Manohara P.J. Senaratne, Josie T. Y. Chow, Paul Cheung-Lung Choi, Tsz-Ngai Chan
Publikováno v:
PLoS ONE
PLoS ONE, Vol 15, Iss 9, p e0239675 (2020)
PLoS ONE, Vol 15, Iss 9, p e0239675 (2020)
Fabry Disease (FD) is a systemic disorder that can result in cardiovascular, renal, and neurovascular disease leading to reduced life expectancy. FD should be considered in the differential of all patients with unexplained left ventricular hypertroph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5aaa0e5502a08ac17feb275361eb7de8
http://europepmc.org/articles/PMC7521938
http://europepmc.org/articles/PMC7521938
Publikováno v:
American journal of medical genetics. Part AREFERENCES. 182(1)
CHARGE syndrome (CS) is a multiple congenital anomalies condition with the majority of cases caused by dominant loss-of-function mutations of the CHD7 gene. It is clinically characterized by coloboma of the eyes, heart defects, choanal atresia, retar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c52d34036753dfc05c1163acac798402
https://pubmed.ncbi.nlm.nih.gov/32804436
https://pubmed.ncbi.nlm.nih.gov/32804436
Autor:
Bun Sheng, Polakit Teekakirikul, Erik Fung, Ka-Tak Wong, Kevin Kh Kam, Yiting Fan, Alex Pw Lee, David K. H. Chan, Joseph Ys Chan, Josie Chow
Publikováno v:
Keynote Lecture.
Fabry disease (FD) is an X-linked inherited lysosomal storage disorder that results from mutations in the α-galactosidase A gene (GLA), leading to deficient alpha-galactosidase A (α-GalA) activity and subsequent accumulation of globotriaosylceramid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9152df01d9479105c014e9e23f2d2676
https://doi.org/10.1136/heartasia-2019-apahff.31
https://doi.org/10.1136/heartasia-2019-apahff.31
Autor:
Ho Ming Luk, David K H Chan, Ivan F M Lo, Connie O.Y. Fung, Tony M F Tong, Stephen T.S. Lam, Kent K.S. Lai, Edgar W L Hau, Albert C.F. Lam, Daniel H C Chan
Publikováno v:
Journal of Genetics and Genomics. 39:191-194
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d095e58841d045037277f35125a9a84
https://doi.org/10.1016/j.jgg.2012.02.005
https://doi.org/10.1016/j.jgg.2012.02.005
Autor:
Symphorosa Shing Chee Chan, Stephen T.S. Lam, Terence T. Lao, Selina M. W. Pang, David K H Chan, Kwong Wai Choy
Publikováno v:
International urogynecology journal. 21(5)
We aimed to compare the incidence of urinary incontinence in women with Marfan syndrome and controls, hypothesizing that connective tissue abnormality could contribute to urinary incontinence.A cross-sectional historical cohort study was conducted on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fde7814d0a1826805b44e9764c5755e2
https://pubmed.ncbi.nlm.nih.gov/20066398
https://pubmed.ncbi.nlm.nih.gov/20066398
Autor:
Sadasivan, Chandu1,2 (AUTHOR), Chow, Josie T. Y.3 (AUTHOR), Sheng, Bun4 (AUTHOR), Chan, David K. H.5 (AUTHOR), Fan, Yiting3,6 (AUTHOR), Choi, Paul C. L.7 (AUTHOR), Wong, Jeffrey K. T.8 (AUTHOR), Tong, Mabel M. B.9 (AUTHOR), Chan, Tsz-Ngai3 (AUTHOR), Fung, Erik3 (AUTHOR), Kam, Kevin K. H.3 (AUTHOR), Chan, Joseph Y. S.3 (AUTHOR), Chi, Wai-Kin3 (AUTHOR), Paterson, D. Ian1,2 (AUTHOR), Senaratne, Manohara1,10 (AUTHOR), Brass, Neil1,11 (AUTHOR), Oudit, Gavin Y.1,2 (AUTHOR) alexpwlee@cuhk.edu.hk, Lee, Alex P. W.3,6 (AUTHOR) alexpwlee@cuhk.edu.hk
Publikováno v:
PLoS ONE. 9/28/2020, Vol. 15 Issue 9, p1-13. 13p.
Publikováno v:
Women's Health Weekly; 7/25/2024, p516-516, 1p
Publikováno v:
American Journal of Medical Genetics. Part A; Jan2020, Vol. 182 Issue 1, p15-19, 5p