Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jasmine Chew Yin Goh"'
Autor:
Gabrielle Stinton, Jane A. Lieviant, Sylvia Kam, Jiin Ying Lim, Jasmine Chew-Yin Goh, Weng Khong Lim, Gareth Baynam, Tele Tan, Duc-Son Pham, Saumya Shekhar Jamuar
Publikováno v:
Rare, Vol 1, Iss , Pp 100007- (2023)
Leveraging Artificial Intelligence (AI) within the rare disease diagnostic odyssey can facilitate a decrease in diagnostic times and an increase in diagnostic rates. Among the steps involved in the odyssey, this project focused on utilizing AI to aut
Externí odkaz:
https://doaj.org/article/322f328574b045dab9429b0b8a61fc93
Autor:
Thurston Yan Jia Heng, Jin Rong Ow, Ai Ling Koh, James Soon Chuan Lim, Christine Bee Keow Ong, Jasmine Chew Yin Goh, Jiin Ying Lim, Fang Kuan Chiou, Jamuar, Saumya Shekhar
Publikováno v:
Clinical Dysmorphology; Jan2024, Vol. 33 Issue 1, p43-49, 7p
Autor:
Theresa Shu Wen Toh, Kok Wee Chong, Ee Shien Tan, Anne Eng Neo Goh, Si Hui Goh, Teck Wah Ting, Jasmine Chew Yin Goh
Publikováno v:
Asian Pacific Journal of Allergy and Immunology.
BACKGROUND Enzyme replacement therapy significantly reduces morbidity and mortality in patients with Pompe disease. Development of hypersensitivity reactions to enzyme replacement therapy is common and can adversely affect disease outcomes when treat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fb23bd8f7b1e99f3f6f10993b140ed1
https://doi.org/10.12932/ap-060919-0638
https://doi.org/10.12932/ap-060919-0638
Autor:
Joanna Y.L. Tung, Katta M. Girisha, Paul Kruszka, Nicole Fleischer, Engy A. Ashaat, E.V. Badoe, Dalia Farouk Hussen, Neer Shoba Chitrakar, Angélica Moresco, Neveen A. Ashaat, Olufemi Fasanmade, Siddaramappa J. Patil, Mona O. El Ruby, André Mégarbané, Johnathan Watts, Karen Fieggen, Gary T. K. Mok, Dhanya Yesodharan, Milagros M. Dueñas-Roque, Ezana Lulseged, Cedrik Tekendo-Ngongang, Sarah Savage, Saumya Shekhar Jamuar, Vajira H. W. Dissanayake, Nirmala D. Sirisena, Sultana M.H. Faradz, Antonio Richieri-Costa, Kelly L. Jones, Jasmine Chew Yin Goh, Brenda C. Iriele, María Beatriz de Herreros, Brian H.Y. Chung, Godfrey Mutashambara Rwegerera, María Gabriela Obregon, Yonit A. Addissie, Nydia Rena Benita Sihombing, Teresa Aravena, Shubha R. Phadke, Victoria Huckstadt, C. Sampath Paththinige, Meow-Keong Thong, Neerja Gupta, Agustini Utari, Sheela Nampoothiri, Elizabeth Eberechi Oyenusi, Ekanem N. Ekure, Maximilian Muenke, Rupesh Mishra, Oluwarotimi Bolaji Olopade, Annette Uwineza, Vorasuk Shotelersuk, Ambroise Wonkam
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Am J Med Genet A
Universidade de São Paulo (USP)
instacron:USP
Am J Med Genet A
Turner syndrome (TS) is a common multiple congenital anomaly syndrome resulting from complete or partial absence of the second X chromosome. TS presents with short stature, infertility secondary to ovarian dysgenesis, cardiac and renal anomalies, cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf516dfd88789c7ce7186e90a9e30000
Autor:
Shazia Khan, Ene-Choo Tan, Jiin Ying Lim, Pamela Si-Min Ng, Saumya Shekhar Jamuar, Grace Lin, Jasmine Chew Yin Goh, Heming Wei
Publikováno v:
Clinical dysmorphology. 28(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94db1659d6ea7b57ae7912edd54e6434
https://pubmed.ncbi.nlm.nih.gov/31490282
https://pubmed.ncbi.nlm.nih.gov/31490282