Towards a global partnership model in interprofessional education for cross-sector problem-solving

Autor: Fraide Ganotice, Binbin Zheng, Pauline Yeung Ng, Siu Chung Leung, Elizabeth Ann Barrett, Hoi Yan Celia Chan, Chad W. N. Chan, Kit Wa Sherry Chan, Linda Chan, M. K. Karen Chan, Siu Ling Polly Chan, So Ching Sarah Chan, Esther W. Y. Chan, Julie Chen, Yuet Ying Jessica Cheuk, Yin Kei Doris Chong, Yin Man Amy Chow, Kwok Pui Jody Chu, Hon Yin Brian Chung, Shun Yee Amy Ho, Julienne Jen, Jingwen Jin, Ui Soon Khoo, Ho Yan Angie Lam, May P. S. Lam, Suk Fun Veronica Lam, Pamela Pui-Wah Lee, Jetty Chung-Yung Lee, Chung Yin Feona Leung, Anna K. Y. Leung, Xiang Lin, Rebecca K. W. Liu, Wei Qun Vivian Lou, Pauline Luk, Lai Han Zoe Ng, Yee Man Alina Ng, Tin Wai Terry Ng, Lok Man Mary See, Jiangang Shen, Xiaoai Shen, Grace Szeto, Eliza Y. T. Tam, Kelvin Kai-Wang To, Wan-Yee Winnie Tso, Dana Vackova, Ning Wang, Runjia Wang, Hoi Yan Gloria Wong, K. T. Janet Wong, M. Y. Anita Wong, Yuen Ha Janet Wong, Kwan Yuk Jacqueline Yuen, Wai Yee Grace Yuen, Mine Orlu, George L. Tipoe

Publikováno v: BMC Medical Education, Vol 23, Iss 1, Pp 1-12 (2023)

Abstract Objectives A partnership model in interprofessional education (IPE) is important in promoting a sense of global citizenship while preparing students for cross-sector problem-solving. However, the literature remains scant in providing useful

Externí odkaz: https://doaj.org/article/ebd4949210f441118030fa6d2710183c

Clinical and Genetic Spectrums of Pediatric Cardiomyopathies: Experience from a Tertiary Pediatric Cardiology Centre in Hong Kong

Autor: Zhuo Julia Shi, Fong Ting Jeffrey Chau, Sit Yee Kwok, Kit San Yeung, Lee Fong Jasmine Fung, Ka Yee Anna Kwong, Tak Cheung Yung, Hon Yin Brian Chung, Kin Shing Lun

Background Pediatric cardiomyopathies are rare conditions associated with substantial morbidity and mortality. This study aims at reporting the clinical and genetic spectrums of pediatric cardiomyopathy in the single tertiary centre in the Hong Kong.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5bbded36d54ca002b9121ed4e3e1a3b2
https://doi.org/10.21203/rs.3.rs-2207234/v1

Clinical application of whole-genometechnologies of paediatric-onset rare diseases

Autor: Hon-yin, Brian Chung

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fa95fe512858f5d67bc938ca9755b1bb
https://doi.org/10.5353/th_991044088597803414

Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes

Autor: Elise Valkanas, Hon-Yin Brian Chung, Peter Farndon, Patricia M. Zerfas, Oliver Bartsch, Martin Zenker, Jeroen Bakkers, Alexander Hoischen, Feliciano J. Ramos, Eva Bermejo-Sánchez, Haigen Huang, Gijs van Haaften, Lynne A. Wolfe, Taylor Davis, Eduarda Morgana da Silva, Han G. Brunner, W. K. Jacyk, Bruno Dallapiccola, Laura Mazzanti, Cathy A. Stevens, Mieke M. van Haelst, Hanka Venselaar, Cornelius F. Boerkoel, Francesco Brancati, Cynthia J. Tifft, May Christine V. Malicdan, Nathalie Roche, Bert B.A. de Vries, Victor Evangelista de Faria Ferraz, Chyi-Chia Richard Lee, Brian P. Brooks, Farahnaz Sabbagh-Kermani, Federico Tessadori, Denny Schanze, Barbara N. Pusey, Ariana Kariminejad, Valerie Maduro, Janice Lee, Giovanna Zambruno, Shuo Lin, Cédric Le Caignec, Thomas C. Markello, Maria Tsokos, Shannon Marchegiani, Fabiana Martins, William A. Gahl, Anneke T. Vulto-van Silfhout

Publikováno v: American Journal of Human Genetics, 97, 1, pp. 99-110
Marchegiani, S, Davis, T, Tessadori, F, van Haaften, G, Brancati, F, Hoischen, A, Huang, H, Valkanas, E, Pusey, B, Schanze, D, Venselaar, H, Vulto-van Silfhout, A T, Wolfe, L A, Tifft, C J, Zerfas, P M, Zambruno, G, Kariminejad, A, Sabbagh-Kermani, F, Lee, J, Tsokos, M G, Lee, C-C R, Ferraz, V, da Silva, E M, Stevens, C A, Roche, N, Bartsch, O, Farndon, P, Bermejo-Sanchez, E, Brooks, B P, Maduro, V, Dallapiccola, B, Ramos, F J, Chung, H-Y B, Le Caignec, C, Martins, F, Jacyk, W K, Mazzanti, L, Brunner, H G, Bakkers, J, Lin, S, Malicdan, M C V, Boerkoel, C F, Gahl, W A, de Vries, B B A, van Haelst, M M, Zenker, M & Markello, T C 2015, ' Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes ', American journal of human genetics, vol. 97, no. 1, pp. 99-110 . https://doi.org/10.1016/j.ajhg.2015.05.017
American Journal of Human Genetics, 97, 99-110
American Journal of Human Genetics, 97(1), 99. Cell Press
American journal of human genetics, 97(1), 99-110. Cell Press
American Journal of Human Genetics, 97(1), 99-110. Cell Press
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP

Contains fulltext : 153827.pdf (Publisher’s version ) (Open Access) Ablepharon macrostomia syndrome (AMS) and Barber-Say syndrome (BSS) are rare congenital ectodermal dysplasias characterized by similar clinical features. To establish the genetic b

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1749856e024ae1fd6a1491db82f32077
https://doi.org/10.1016/j.ajhg.2015.05.017

Barber-Say Syndrome and Ablepharon-Macrostomia Syndrome: A Patient's View

Autor: Hon-Yin Brian Chung, Raoul C.M. Hennekam, Maura Foresti, Ankur Singh, Kenichi Suga, Francesco Brancati, Marina Gallottini, Albert David, Beatrice De Maria, Oliver Bartsch, Ariana Kariminejad, Martin Zenker, Nathalie Roche, Shannon Marchegiani, Fabiana Martins, Tresia de Jager, Alberto Bianchi, Laura Mazzanti, Bertrand Isidor, Caitlin Sarubbi, Cathy A. Stevens

Publikováno v: MOLECULAR SYNDROMOLOGY
Molecular syndromology, 8(4), 172-178. S. Karger AG

Barber-Say syndrome (BSS) and ablepharon-macrostomia syndrome (AMS) are infrequently reported congenital malformation disorders caused by mutations in the TWIST2 gene. Both are characterized by abnormalities in ectoderm-derived structures and cause a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c23e6b51219ba442b97e54fcc760da4d
http://hdl.handle.net/11697/122117