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Journal of Human Genetics|November 24, 2007
Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: identification of 17 novel mutations and its genetic heterogeneityChloe Miu Mak, Ching-Wan Lam, Sidney Tam, et al.Journal of Human Genetics|February 12, 2020
Erratum to: Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneityChloe Miu Mak, Ching-Wan Lam, Sidney Tam, et al.Brain & Development|July 29, 2022
Guillain-Barré syndrome in children - High occurrence of Miller Fisher syndrome in East Asian regionAnnie Ting Gee Chiu, Ricky Wing Ki Chan, Maggie Lo Yee Yau, et al.Orphanet Journal of Rare Diseases|March 1, 2023
Mitochondrial diseases in Hong Kong: prevalence, clinical characteristics and genetic landscapeTsz-Sum Wong, Kiran M Belaramani, Chun-Kong Chan, et al.Neurology|January 30, 2025
Characterization of Factors Associated With Death in Deceased Patients With Mitochondrial Disorders: A Multicenter Cross-Sectional SurveyAlina Ivaniuk, Irina A Anselm, Aaron Bowen, et al.Pageof 3