Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Han-Chih Hencher Lee"'
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:
Han-Chih Hencher Lee, Nike Kwai-Cheung Lau, Chun-Wing Yeung, Sui-Fun Grace Ng, Kin-Cheong Eric Yau, Chloe Miu Mak
Publikováno v:
Chinese Medical Journal, Vol 131, Iss 18, Pp 2262-2264 (2018)
Externí odkaz:
https://doaj.org/article/ab72ae3ae10e4665b72633d18371de63
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:
Han-Chih Hencher Lee1, Chor-Kwan Ching1 chingck2@ha.org.hk
Publikováno v:
Clinical Biochemist Reviews. 2019, Vol. 40 Issue 4, p187-200. 14p.
Autor:
Hok-Fung Tong, Han-Chih Hencher Lee, Tsz-Yan Tammy Tong, Siu-Fung Lam, Bun Sheng, Kin-Wah Chan, June Kam-Yin Li, Ho-Kee Vicki Tam, Chor-Kwan Ching
Publikováno v:
Journal of diabetes and its complications. 36(3)
m.3243AG-related disease has multi-systemic manifestations including diabetes mellitus. It is uncertain whether metformin would trigger neurological manifestations of this disease. This study aims to review the diagnosis and management of m.3243AG-re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94523836bbfc93e32f5642929b76014a
https://pubmed.ncbi.nlm.nih.gov/35351383
https://pubmed.ncbi.nlm.nih.gov/35351383
Autor:
Frank Ying-Kit Leung, Luen-Cheung Ho, Siu-Ki Timothy Chan, Tsui-Hang Sharon Fung, Hoi-Ki Cynthia Leung, Han-Chih Hencher Lee, Sammy Pak-Lam Chen, Kin-Cheong Eric Yau, Chloe Miu Mak, Shun Wong, Wai-Nang Yau, Kwok-Fan Kwan, Ka-Wah Li
Publikováno v:
Journal of Neuropathology & Experimental Neurology. 78:854-864
KLHL40-related nemaline myopathy is a severe autosomal recessive muscle disorder. The current study describes 4 cases of KLHL40-related nemaline myopathy in Hong Kong ethnic Chinese presenting within 3 years, which are confirmed with clinicopathologi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f0edbacf9155e062810f819eefaaba4
https://doi.org/10.1093/jnen/nlz056
https://doi.org/10.1093/jnen/nlz056
Autor:
Kuen Shum Pang, Wing Lan Cheung, Tony W L Mak, Tat Chong Chow, Sau Wah Ng, Chi On Tang, Suk San Chan, Han Chih Hencher Lee, Ying Hoo Lam, Chun Yiu Law
Publikováno v:
Toxicon. 154:42-49
Introduction Gelsemium poisoning is caused by consumption of the deadly Gelsemium species such as Gelsemium elegans, leading to significant gastrointestinal, neurological and cardio-respiratory toxicities. In 2011 (Cluster 1) and 2012 (Cluster 2), th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc7bf97bedb91835cc7d7bd5d9d934ed
https://doi.org/10.1016/j.toxicon.2018.09.009
https://doi.org/10.1016/j.toxicon.2018.09.009
Autor:
Nike Kwai-Cheung Lau, Kin-Cheong Eric Yau, Chloe Miu Mak, Han-Chih Hencher Lee, Chun-Wing Yeung, Sui-Fun Grace Ng
Publikováno v:
Chinese Medical Journal, Vol 131, Iss 18, Pp 2262-2264 (2018)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1f33338ba06c0c333b21a33d0659a51
https://doi.org/10.4103/0366-6999.240812
https://doi.org/10.4103/0366-6999.240812
Autor:
Han-Chih Hencher Lee, TH Tsoi, Shun Wong, Ying-Kit Frank Leung, Tina Yee-Ching Chan, Chloe Miu Mak, Tze-Chin Gene Lau, Hok-Fung Tong, Bun Sheng, Richard Li, Chi-Nam Lee, Ka-Ho Lee, Luen-Cheung Ho, Ling-Yin Esther Hung, Tin-Wing Tong, Yuk-Fai Nelson Cheung, Yim-Pui Chu, Ching-Wan Lam, Yue Sandy Cheng, Siu-Hung Li, Chi Terence Li, Nin-Yuan Keith Pan, Albert Yan-Wo Chan, Nim-Chi Amanda Kan, Yat-Pang Michael Fu, Kwok-kwong Lau, Sung-Yan Sue Yeung, Ho-Ying Cory Leung, Hon-Ming Jonas Yeung, Chi-Fung Mark Cheung, Wing-Chi Lisa Au, Sau-Yin Blanka Lee, Tsz-Yan Tammy Tong
Publikováno v:
Clinical geneticsREFERENCES. 97(5)
FLNC-related myofibrillar myopathy could manifest as autosomal dominant late-onset slowly progressive proximal muscle weakness; involvements of cardiac and/or respiratory functions are common. We describe 34 patients in nine families of FLNC-related
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab3bd6a20101194a2d2880bc7f861196
https://pubmed.ncbi.nlm.nih.gov/32022900
https://pubmed.ncbi.nlm.nih.gov/32022900
Autor:
Chor-Kwan Ching, Han-Chih Hencher Lee
Genetic testing has an increasingly important role in the diagnosis and management of cardiac disorders, where it confirms the diagnosis, aids prognostication and risk stratification and guides treatment. A genetic diagnosis in the proband also enabl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0cb55a184d04c54e038188d76a10872
https://europepmc.org/articles/PMC6892704/
https://europepmc.org/articles/PMC6892704/
