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Annals of the Academy of Medicine, Singapore|November 12, 2009
External quality assurance programme for newborn screening of glucose-6-phosphate dehydrogenase deficiencySzu-Hui Chiang, Mei-Ling Fan, Kwang-Jen HsiaoThe Southeast Asian Journal of Tropical Medicine and Public Health|May 24, 2005
Quality assurance program for neonatal screening of glucose-6-phosphate dehydrogenase deficiencySzu-Hui Chiang, Kuei-Fen Wu, Tze-Tze Liu, et al.Journal of Human Genetics|July 16, 2010
Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuriaMei-Ying Liu, Yan-Ling Yang, Ying-Chen Chang, et al.Journal of Human Genetics|January 10, 2014
The mutation spectrum of the phenylalanine hydroxylase (PAH) gene and associated haplotypes reveal ethnic heterogeneity in the Taiwanese populationYing Liang, Miao-Zeng Huang, Cheng-Yi Cheng, et al.Archives of Disease in Childhood|February 24, 2018
Outcomes of neonatal jaundice in TaiwanPei-Chen Tsao, Hsin-Ling Yeh, Yen-Chen Chang, et al.Scientific Reports|July 11, 2020
Long-term neurodevelopmental outcomes of significant neonatal jaundice in Taiwan from 2000-2003: a nationwide, population-based cohort studyPei-Chen Tsao, Hsin-Ling Yeh, Yu-Shih Shiau, et al.Journal of Inherited Metabolic Disease|June 23, 2010
Nationwide survey of extended newborn screening by tandem mass spectrometry in TaiwanDau-Ming Niu, Yin-Hsiu Chien, Chuan-Chi Chiang, et al.Pediatrics|February 23, 2023
Comparing Strategies for Critical Congenital Heart Disease Newborn ScreeningPei-Chen Tsao, Szu-Hui Chiang, Yu-Shih Shiau, et al.Plos One|April 14, 2016
Development of a Newborn Screening Program for Critical Congenital Heart Disease (CCHD) in TaipeiPei-Chen Tsao, Yu-Shih Shiau, Szu-Hui Chiang, et al.Journal of Human Genetics|August 2, 2005
Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiencyYao Bang Lu, Keiko Kobayashi, Miharu Ushikai, et al.Pageof 2