Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Marco Hok-Kung Ho"'
Autor:
Chia-Yu Chu, Tsung-Chieh Yao, I.-Hsin Shih, Chin-Yi Yang, Chan Lee Chin, Sabeera Begum Binti Kader Ibrahim, Suganthi Thevarajah, Leong Kin Fon, Marco Hok-Kung Ho, Chow Chung Mo, Chow Pok Yu, Steven King-Fan Loo, Thomas Luger
Publikováno v:
Dermatology and Therapy, Vol 13, Iss 3, Pp 717-727 (2023)
Abstract Atopic dermatitis (AD) is a common chronic, multisystem inflammatory skin disease in pediatric patients. There has been an increase in the incidence of AD in the pediatric population of the Asia–Pacific region. Studies have shown that gene
Externí odkaz:
https://doaj.org/article/c8e1decd453647e88fd37f685b509c42
Autor:
Timothy Lok-Hin Chiu, Daniel Leung, Koon-Wing Chan, Hok Man Yeung, Chung-Yin Wong, Huawei Mao, Jianxin He, Pandiarajan Vignesh, Weiling Liang, Woei Kang Liew, Li-Ping Jiang, Tong-Xin Chen, Xiang-Yuan Chen, Yin-Bo Tao, Yong-Bin Xu, Hsin-Hui Yu, Alta Terblanche, David Christopher Lung, Cheng-Rong Li, Jing Chen, Man Tian, Brian Eley, Xingtian Yang, Jing Yang, Wen Chin Chiang, Bee Wah Lee, Deepti Suri, Amit Rawat, Anju Gupta, Surjit Singh, Wilfred Hing Sang Wong, Gilbert T. Chua, Jaime Sou Da Rosa Duque, Kai-Ning Cheong, Patrick Chun-Yin Chong, Marco Hok-Kung Ho, Tsz-Leung Lee, Wanling Yang, Pamela P. Lee, Yu Lung Lau
Publikováno v:
Frontiers in Immunology, Vol 12 (2022)
BackgroundChronic granulomatous disease (CGD) is an inborn error of immunity (IEI), characterised by recurrent bacterial and fungal infections. It is inherited either in an X-linked (XL) or autosomal recessive (AR) mode. Phenome refers to the entire
Externí odkaz:
https://doaj.org/article/4e9bbac58e3d4de0a00a92ba177095a5
Autor:
Karen Ka Yan Leung, Jaime Sou Rosa Duque, Kwong-Man Yu, Kai-Ning Cheong, Patrick Chun-Yin Chong, Marco Hok-Kung Ho, Pak-Cheong Chow
Publikováno v:
BMC Pediatrics, Vol 19, Iss 1, Pp 1-7 (2019)
Abstract Background Idiopathic systemic capillary leak syndrome (ISCLS) is rare, and there has been about 32 cases reported in children worldwide since this disorder was first described in 1960. Clinical guidelines on the management approach stemming
Externí odkaz:
https://doaj.org/article/e6d8d8210871455ab6061282c3012bb0
Autor:
Koon-Wing Chan, Chung-Yin Wong, Daniel Leung, Xingtian Yang, Susanna F. S. Fok, Priscilla H. S. Mak, Lei Yao, Wen Ma, Huawei Mao, Xiaodong Zhao, Weiling Liang, Surjit Singh, Mohamed-Ridha Barbouche, Jian-Xin He, Li-Ping Jiang, Woei-Kang Liew, Minh Huong Thi Le, Dina Muktiarti, Fatima Johanna Santos-Ocampo, Reda Djidjik, Brahim Belaid, Intan Hakimah Ismail, Amir Hamzah Abdul Latiff, Way Seah Lee, Tong-Xin Chen, Jinrong Liu, Runming Jin, Xiaochuan Wang, Yin Hsiu Chien, Hsin-Hui Yu, Dinesh Raj, Revathi Raj, Jenifer Vaughan, Michael Urban, Sylvia van den Berg, Brian Eley, Anselm Chi-Wai Lee, Mas Suhaila Isa, Elizabeth Y. Ang, Bee Wah Lee, Allen Eng Juh Yeoh, Lynette P. Shek, Nguyen Ngoc Quynh Le, Van Anh Thi Nguyen, Anh Phan Nguyen Lien, Regina D. Capulong, Joanne Michelle Mallillin, Jose Carlo Miguel M. Villanueva, Karol Anne B. Camonayan, Michelle De Vera, Roxanne J. Casis-Hao, Rommel Crisenio M. Lobo, Ruby Foronda, Vicky Wee Eng Binas, Soraya Boushaki, Nadia Kechout, Gun Phongsamart, Siriporn Wongwaree, Chamnanrua Jiratchaya, Mongkol Lao-Araya, Muthita Trakultivakorn, Narissara Suratannon, Orathai Jirapongsananuruk, Teerapol Chantveerawong, Wasu Kamchaisatian, Lee Lee Chan, Mia Tuang Koh, Ke Juin Wong, Siew Moy Fong, Meow-Keong Thong, Zarina Abdul Latiff, Lokman Mohd Noh, Rajiva de Silva, Zineb Jouhadi, Khulood Al-Saad, Pandiarajan Vignesh, Ankur Kumar Jindal, Amit Rawat, Anju Gupta, Deepti Suri, Jing Yang, Elaine Yuen-Ling Au, Janette Siu-Yin Kwok, Siu-Yuen Chan, Wayland Yuk-Fun Hui, Gilbert T. Chua, Jaime Rosa Duque, Kai-Ning Cheong, Patrick Chun Yin Chong, Marco Hok Kung Ho, Tsz-Leung Lee, Wilfred Hing-Sang Wong, Wanling Yang, Pamela P. Lee, Wenwei Tu, Xi-Qiang Yang, Yu Lung Lau
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
To address inborn errors of immunity (IEI) which were underdiagnosed in resource-limited regions, our centre developed and offered free genetic testing for the most common IEI by Sanger sequencing (SS) since 2001. With the establishment of The Asian
Externí odkaz:
https://doaj.org/article/e0001b5e732a40f496811e7631968120
Autor:
Mehul Sharma, Daniel Leung, Mana Momenilandi, Lauren C.W. Jones, Lucia Pacillo, Alyssa E. James, Jill R. Murrell, Selket Delafontaine, Jesmeen Maimaris, Maryam Vaseghi-Shanjani, Kate L. Del Bel, Henry Y. Lu, Gilbert T. Chua, Silvia Di Cesare, Oriol Fornes, Zhongyi Liu, Gigliola Di Matteo, Maggie P. Fu, Donato Amodio, Issan Yee San Tam, Gavin Shueng Wai Chan, Ashish A. Sharma, Joshua Dalmann, Robin van der Lee, Géraldine Blanchard-Rohner, Susan Lin, Quentin Philippot, Phillip A. Richmond, Jessica J. Lee, Allison Matthews, Michael Seear, Alexandra K. Turvey, Rachael L. Philips, Terri F. Brown-Whitehorn, Christopher J. Gray, Kosuke Izumi, James R. Treat, Kathleen H. Wood, Justin Lack, Asya Khleborodova, Julie E. Niemela, Xingtian Yang, Rui Liang, Lin Kui, Christina Sze Man Wong, Grace Wing Kit Poon, Alexander Hoischen, Caspar I. van der Made, Jing Yang, Koon Wing Chan, Jaime Sou Da Rosa Duque, Pamela Pui Wah Lee, Marco Hok Kung Ho, Brian Hon Yin Chung, Huong Thi Minh Le, Wanling Yang, Pejman Rohani, Ali Fouladvand, Hassan Rokni-Zadeh, Majid Changi-Ashtiani, Mohammad Miryounesi, Anne Puel, Mohammad Shahrooei, Andrea Finocchi, Paolo Rossi, Beatrice Rivalta, Cristina Cifaldi, Antonio Novelli, Chiara Passarelli, Stefania Arasi, Dominique Bullens, Kate Sauer, Tania Claeys, Catherine M. Biggs, Emma C. Morris, Sergio D. Rosenzweig, John J. O’Shea, Wyeth W. Wasserman, H. Melanie Bedford, Clara D.M. van Karnebeek, Paolo Palma, Siobhan O. Burns, Isabelle Meyts, Jean-Laurent Casanova, Jonathan J. Lyons, Nima Parvaneh, Anh Thi Van Nguyen, Caterina Cancrini, Jennifer Heimall, Hanan Ahmed, Margaret L. McKinnon, Yu Lung Lau, Vivien Béziat, Stuart E. Turvey
Publikováno v:
Journal of Experimental Medicine, 220
Journal of Experimental Medicine, 220, 5
Journal of Experimental Medicine, 220, 5
STAT6 (signal transducer and activator of transcription 6) is a transcription factor that plays a central role in the pathophysiology of allergic inflammation. We have identified 16 patients from 10 families spanning three continents with a profound
Autor:
Ka Keung Ho, Kwun Cheung Hau, Alson Wai Ming Chan, Davis Yung Chan, Marco Hok Kung Ho, Steven King Fan Loo, Tam Yat Cheung Alfred, Giovanni Pellacani, Adelaide A. Hebert, Lisa Braganza
Publikováno v:
CosmoDerma. 2:47
The Dermatology Advisory Board on Atopic Dermatitis from Asian Medical Expert Academy compiles current evidence-based approach review in managing atopic dermatitis (AD) among Asians. Electronic searches were performed to retrieve relevant published p
Autor:
Anderson Dik Wai Luk, Pamela P. Lee, Huawei Mao, Koon-Wing Chan, Xiang Yuan Chen, Tong-Xin Chen, Jian Xin He, Nadia Kechout, Deepti Suri, Yin Bo Tao, Yong Bin Xu, Li Ping Jiang, Woei Kang Liew, Orathai Jirapongsananuruk, Tassalapa Daengsuwan, Anju Gupta, Surjit Singh, Amit Rawat, Amir Hamzah Abdul Latiff, Anselm Chi Wai Lee, Lynette P. Shek, Thi Van Anh Nguyen, Tek Jee Chin, Yin Hsiu Chien, Zarina Abdul Latiff, Thi Minh Huong Le, Nguyen Ngoc Quynh Le, Bee Wah Lee, Qiang Li, Dinesh Raj, Mohamed-Ridha Barbouche, Meow-Keong Thong, Maria Carmen D. Ang, Xiao Chuan Wang, Chen Guang Xu, Hai Guo Yu, Hsin-Hui Yu, Tsz Leung Lee, Felix Yat Sun Yau, Wilfred Hing-Sang Wong, Wenwei Tu, Wangling Yang, Patrick Chun Yin Chong, Marco Hok Kung Ho, Yu Lung Lau
Publikováno v:
Frontiers in Immunology
Frontiers in Immunology, Frontiers, 2017, 8, pp.808. ⟨10.3389/fimmu.2017.00808⟩
Frontiers in Immunology, Vol 8 (2017)
Frontiers in Immunology, Frontiers, 2017, 8, pp.808. ⟨10.3389/fimmu.2017.00808⟩
Frontiers in Immunology, Vol 8 (2017)
International audience; Background: Severe combined immunodeficiency (SCID) is fatal unless treated with hematopoietic stem cell transplant. Delay in diagnosis is common without newborn screening. Family history of infant death due to infection or kn
Autor:
Jing, Zhang, Lu, Zhang, Yan, Zhang, Jing, Yang, Mengbiao, Guo, Liangdan, Sun, Hai-Feng, Pan, Nattiya, Hirankarn, Dingge, Ying, Shuai, Zeng, Tsz Leung, Lee, Chak Sing, Lau, Tak Mao, Chan, Alexander Moon Ho, Leung, Chi Chiu, Mok, Sik Nin, Wong, Ka Wing, Lee, Marco Hok Kung, Ho, Pamela Pui Wah, Lee, Brian Hon-Yin, Chung, Chun Yin, Chong, Raymond Woon Sing, Wong, Mo Yin, Mok, Wilfred Hing Sang, Wong, Kwok Lung, Tong, Niko Kei Chiu, Tse, Xiang-Pei, Li, Yingyos, Avihingsanon, Pornpimol, Rianthavorn, Thavatchai, Deekajorndej, Kanya, Suphapeetiporn, Vorasuk, Shotelersuk, Shirley King Yee, Ying, Samuel Ka Shun, Fung, Wai Ming, Lai, Maria-Mercè, Garcia-Barceló, Stacey S, Cherny, Pak Chung, Sham, Yong, Cui, Sen, Yang, Dong Qing, Ye, Xue-Jun, Zhang, Yu Lung, Lau, Wanling, Yang
Publikováno v:
Arthritisrheumatology (Hoboken, N.J.). 67(11)
Previous genome-wide association studies (GWAS), which were mainly based on single-variant analysis, have identified many systemic lupus erythematosus (SLE) susceptibility loci. However, the genetic architecture of this complex disease is far from be
Autor:
Jing, Zhang, Yan, Zhang, Lu, Zhang, Jing, Yang, Dingge, Ying, Shuai, Zeng, Tsz Leung, Lee, Chak Sing, Lau, Tak Mao, Chan, Alexander Moon Ho, Leung, Chi Chiu, Mok, Sik Nin, Wong, Ka Wing, Lee, Marco Hok Kung, Ho, Pamela Pui Wah, Lee, Brian Hon-Yin, Chung, Chun Yin, Chong, Raymond Woon Sing, Wong, Mo Yin, Mok, Wilfred Hing Sang, Wong, Yu Lung, Lau, Wanling, Yang
Publikováno v:
Annals of human genetics. 77(4)
T-helper cells that produce IL-17 (Th17 cells) are a subset of CD4(+) T-cells with pathological roles in autoimmune diseases including systemic lupus erythematosus (SLE), and ETS1 is a negative regulator of Th17 cell differentiation. Our previous wor
Autor:
Jun, Yang, Daniel Ka Leung, Cheuk, Shau Yin, Ha, Alan Kwok Shing, Chiang, Tsz Leung, Lee, Marco Hok Kung, Ho, Godfrey Chi Fung, Chan
Publikováno v:
Pediatric transplantation. 16(7)
aGVHD of the GI tract is common after allogeneic HSCT. Corticosteroids are the mainstay of treatment. Recent data suggest infliximab might be beneficial for steroid refractory aGVHD. We reviewed our experience in 10 pediatric patients who developed s