Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Che Kwan Ma"'
Autor:
Tsz-sum Wong, Kiran M. Belaramani, Chun-kong Chan, Wing-ki Chan, Wai-lun Larry Chan, Shek-kwan Chang, Sing-ngai Cheung, Ka-yin Cheung, Yuk-fai Cheung, Shuk-ching Josephine Chong, Chi-kwan Jasmine Chow, Hon-yin Brian Chung, Sin-ying Florence Fan, Wai-ming Joshua Fok, Ka-wing Fong, Tsui-hang Sharon Fung, Kwok-fai Hui, Ting-hin Hui, Joannie Hui, Chun-hung Ko, Min-chung Kwan, Mei-kwan Anne Kwok, Sung-shing Jeffrey Kwok, Moon-sing Lai, Yau-on Lam, Ching-wan Lam, Ming-chung Lau, Chun-yiu Eric Law, Wing-cheong Lee, Han-chih Hencher Lee, Chin-nam Lee, Kin-hang Leung, Kit-yan Leung, Siu-hung Li, Tsz-ki Jacky Ling, Kam-tim Timothy Liu, Fai-man Lo, Hiu-tung Lui, Ching-on Luk, Ho-ming Luk, Che-kwan Ma, Karen Ma, Kam-hung Ma, Yuen-ni Mew, Alex Mo, Sui-fun Ng, Wing-kit Grace Poon, Richard Rodenburg, Bun Sheng, Jan Smeitink, Cheuk-ling Charing Szeto, Shuk-mui Tai, Choi-ting Alan Tse, Li-yan Lilian Tsung, Ho-ming June Wong, Wing-yin Winnie Wong, Kwok-kui Wong, Suet-na Sheila Wong, Chun-nei Virginia Wong, Wai-shan Sammy Wong, Chi-kin Felix Wong, Shun-ping Wu, Hiu-fung Jerome Wu, Man-mut Yau, Kin-cheong Eric Yau, Wai-lan Yeung, Hon-ming Jonas Yeung, Kin-keung Edwin Yip, Pui-hong Terence Young, Gao Yuan, Yuet-ping Liz Yuen, Chi-lap Yuen, Cheuk-wing Fung
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-11 (2023)
Abstract Objective To determine the prevalence of mitochondrial diseases (MD) in Hong Kong (HK) and to evaluate the clinical characteristics and genetic landscape of MD patients in the region. Methods This study retrospectively reviewed the phenotypi
Externí odkaz:
https://doaj.org/article/a751dccace7643758afd7f2cea4c2452
Autor:
Anna Ka-Yee Kwong, Mandy Ho-Yin Tsang, Jasmine Lee-Fong Fung, Christopher Chun-Yu Mak, Kate Lok-San Chan, Richard J. T. Rodenburg, Monkol Lek, Shushu Huang, Sander Pajusalu, Man-Mut Yau, Cheung Tsoi, Sharon Fung, Kam-Tim Liu, Che-Kwan Ma, Sheila Wong, Eric Kin-Cheong Yau, Shuk-Mui Tai, Eva Lai-Wah Fung, Nick Shun-Ping Wu, Li-Yan Tsung, Jan Smeitink, Brian Hon-Yin Chung, Cheuk-Wing Fung
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-12 (2021)
Abstract Background Movement disorders are a group of heterogeneous neurological diseases including hyperkinetic disorders with unwanted excess movements and hypokinetic disorders with reduction in the degree of movements. The objective of our study
Externí odkaz:
https://doaj.org/article/a75fac8f007d420a85ab11522cca237a
Autor:
Mandy H.Y. Tsang, Anna K.Y. Kwong, Kate L.S. Chan, Jasmine L.F. Fung, Mullin H.C. Yu, Christopher C.Y. Mak, Kit-San Yeung, Richard J.T. Rodenburg, Jan A.M. Smeitink, Rachel Chan, Thomas Tsoi, Joannie Hui, Shelia S.N Wong, Shuk-Mui Tai, Victor C.M. Chan, Che-Kwan Ma, Sharon T.H. Fung, Shun-Ping Wu, W.K. Chak, Brian H.Y. Chung, Cheuk-Wing Fung
Publikováno v:
Human Genomics, Vol 14, Iss 1, Pp 1-10 (2020)
Abstract Background Mitochondrial diseases (MDs) are a group of clinically and genetically heterogeneous disorders characterized by defects in oxidative phosphorylation. Since clinical phenotypes of MDs may be non-specific, genetic diagnosis is cruci
Externí odkaz:
https://doaj.org/article/8385714f30b847afbf46e0c0a43d9134
Guillain-Barré syndrome in children – High occurrence of Miller Fisher syndrome in East Asian region
Autor:
Annie Ting Gee Chiu, Ricky Wing Ki Chan, Maggie Lo Yee Yau, Angus Chi Lap Yuen, Alva King Fai Lam, Shirley Wai Yin Lau, Alan Ming Chung Lau, Sharon Tsui Hang Fung, Kam Hung Ma, Christine Wai Ling Lau, Man Mut Yau, Chun Hung Ko, Kwing Wan Tsui, Che Kwan Ma, Shuk Mui Tai, Eric Kin Cheong Yau, Eva Fung, Shun Ping Wu, Karen Ling Kwong, Sophelia Hoi Shan Chan
Publikováno v:
Brain and Development. 44:715-724
Guillain-Barré syndrome (GBS) is a rare acquired immune-mediated polyneuropathy. Updated population-based data concerning paediatric GBS is needed.Paediatric patients aged below 18 years diagnosed with GBS between 2009 and 2018 in all 11 paediatric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1f93ef018643f52724787807923e27f
https://doi.org/10.1016/j.braindev.2022.07.003
https://doi.org/10.1016/j.braindev.2022.07.003
Autor:
Kwong, Anna Ka-Yee, Tsang, Mandy Ho-Yin, Fung, Jasmine Lee-Fong, Mak, Christopher Chun-Yu, Chan, Kate Lok-San, Rodenburg, Richard J. T., Monkol Lek, Shushu Huang, Pajusalu, Sander, Man-Mut Yau, Cheung Tsoi, Fung, Sharon, Kam-Tim Liu, Che-Kwan Ma, Wong, Sheila, Yau, Eric Kin-Cheong, Shuk-Mui Tai, Fung, Eva Lai-Wah, Wu, Nick Shun-Ping, Tsung, Li-Yan, Smeitink, Jan, Chung, Brian Hon-Yin, Cheuk-Wing Fung
Additional file 1: Supplementary table 1: 272 movement disorder-related genes; Supplementary table 2: 244 mitochondrial disease-related genes; Supplementary table 3: Clinical features of patients with no genetic variant found.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e92b16e9fa005ae3b12231d068a9919
Autor:
Kam-Tim Liu, Nick Shun-Ping Wu, Kate Lok-San Chan, Man-Mut Yau, Jan A.M. Smeitink, Li-Yan Tsung, Cheung Tsoi, Christopher C.Y. Mak, Mandy H.Y. Tsang, Sheila Wong, Brian H.Y. Chung, Anna Ka-Yee Kwong, Jasmine L.F. Fung, Richard J. Rodenburg, Shuk-Mui Tai, Eva Lai-Wah Fung, Monkol Lek, Sharon T. H. Fung, Eric Kin-Cheong Yau, Shushu Huang, Cheuk-Wing Fung, Sander Pajusalu, Che-Kwan Ma
Publikováno v:
Orphanet Journal of Rare Diseases, 16
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-12 (2021)
Orphanet Journal of Rare Diseases, 16, 1
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-12 (2021)
Orphanet Journal of Rare Diseases, 16, 1
Background Movement disorders are a group of heterogeneous neurological diseases including hyperkinetic disorders with unwanted excess movements and hypokinetic disorders with reduction in the degree of movements. The objective of our study is to inv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f826e11ecd98120aa7cf64344e958cb4
http://hdl.handle.net/2066/230163
http://hdl.handle.net/2066/230163
Autor:
Li-Yan Tsung, Monkol Lek, Sander Pajusalu, Che-Kwan Ma, Kate Lok-San Chan, Eva Lai-Wah Fung, Cheuk-Wing Fung, Mandy H.Y. Tsang, Man-Mut Yau, Shuk-Mui Tai, Jasmine L.F. Fung, Richard J. Rodenburg, Sharon T. H. Fung, Kam-Tim Liu, Cheung Tsoi, Shushu Huang, Jan A.M. Smeitink, Nick Shun-Ping Wu, Christopher C.Y. Mak, Brian H.Y. Chung, Sheila Wong, Anna Ka-Yee Kwong, Eric Kin-Cheong Yau
Background: Movement disorders are a group of heterogeneous neurological diseases including hyperkinetic disorders with unwanted excess movements and hypokinetic disorders with reduction in the degree of movements. The objective of our study is to in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::819aafdceb3288e1b79c63f1cd713c2c
https://doi.org/10.21203/rs.3.rs-101211/v1
https://doi.org/10.21203/rs.3.rs-101211/v1
Autor:
Brian H.Y. Chung, Che-Kwan Ma, Kate L.S. Chan, Shuk-Mui Tai, Anna K.Y. Kwong, Mandy H.Y. Tsang, Rachel Chan, Cheuk-Wing Fung, Jan A.M. Smeitink, Christopher C.Y. Mak, W.K. Chak, Shelia S.N Wong, Sharon T. H. Fung, Thomas Tsoi, Jasmine L.F. Fung, Richard J. Rodenburg, Shun-Ping Wu, Joannie Hui, Kit San Yeung, Victor Chi Man Chan, Mullin H.C. Yu
Publikováno v:
Human Genomics, 14, 1
Human Genomics, 14
Human Genomics
Human Genomics, Vol 14, Iss 1, Pp 1-10 (2020)
Human Genomics, 14
Human Genomics
Human Genomics, Vol 14, Iss 1, Pp 1-10 (2020)
Background Mitochondrial diseases (MDs) are a group of clinically and genetically heterogeneous disorders characterized by defects in oxidative phosphorylation. Since clinical phenotypes of MDs may be non-specific, genetic diagnosis is crucial for gu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71f76c3f6d0c1f90ec6f5ea53d48d0f8
https://doi.org/10.1186/s40246-020-00278-0
https://doi.org/10.1186/s40246-020-00278-0
Autor:
Mandy Ho-Yin Tsang, Anna Ka-Yee Kwong, Kate Lok-San Chan, Jasmine Lee-Fong Fung, Mullin Ho-Chung Yu, Christopher Chun-Yu Mak, Kit-San Yeung, Richard J.T. Rodenburg, Jam A.M. Smeitink, Rachel Chan, Thomas Tsoi, Joannie Hui, Sheila Suet-Na Wong, Shuk-Mui Tai, Victor Chi-Man Chan, Che-Kwan Ma, Tsiu-Hang Sharon Fung, Shun-Ping Wu, WK Chan, Brian Hon-Yin Chung, Cheuk-wing Fung
Background Mitochondrial diseases (MDs) are a group of clinically and genetically heterogeneous disorders characterized by defects in oxidative phosphorylation. Since clinical phenotypes of MDs may be non-specific, genetic diagnosis is crucial for gu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8abf1db67e9dcdc1316872c588d761f5
https://doi.org/10.21203/rs.3.rs-23585/v2
https://doi.org/10.21203/rs.3.rs-23585/v2
Publikováno v:
Journal of Paediatrics and Child Health. 47:373-377
Aim: Rotavirus and norovirus gastro-enteritis (GE) are common in children. Complications, except severe dehydration, are rare. Rotavirus was known to cause seizures and even GE encephalopathy, but these complications are less described in norovirus i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a6282cbd9a0c16c5a03b3fe997497c8
https://doi.org/10.1111/j.1440-1754.2010.01986.x
https://doi.org/10.1111/j.1440-1754.2010.01986.x