S. Chiang

发表

Development of a Newborn Screening Program for Critical Congenital Heart Disease (CCHD) in Taipei

K. Hsiao, Pei-Chen Tsao, W. Soong, 2016, PloS one.

Nationwide survey of extended newborn screening by tandem mass spectrometry in Taiwan

Yin-Hsiu Chien, Wuh-Liang Hwu, Shu-Min Kao, 2010, Journal of Inherited Metabolic Disease.

The universal newborn hearing screening program of Taipei City.

K. Hsiao, Yu-Shih Shiau, S. Chiang, 2013, International journal of pediatric otorhinolaryngology.

Tetrahydrobiopterin-deficient hyperphenylalaninemia in the Chinese.

S. Chiang, T. T. Liu, S. J. Wu, 2001, Clinica chimica acta; international journal of clinical chemistry.

Quality assurance program for neonatal screening of glucose-6-phosphate dehydrogenase deficiency.

K. Hsiao, Tze-tze Liu, S. Chiang, 2003, The Southeast Asian journal of tropical medicine and public health.

Long-term neurodevelopmental outcomes of significant neonatal jaundice in Taiwan from 2000–2003: a nationwide, population-based cohort study

K. Hsiao, P. Chiang, M. Jeng, 2020, Scientific Reports.

Mutation analysis of the 6‐pyruvoyl‐tetrahydropterin synthase gene in Chinese hyperphenylalaninemia caused by tetrahydrobiopterin synthesis deficiency

K. Hsiao, Tze-tze Liu, S. Chiang, 1998, Human mutation.

Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiency

Dong Hwan Lee, L. Tsui, K. Hsiao, 2005, Journal of Human Genetics.

Outcomes of neonatal jaundice in Taiwan

K. Hsiao, P. Chiang, M. Jeng, 2018, Archives of Disease in Childhood.

Neonatal Thyroid Function Is Unaffected by Maternal Topical Iodine Disinfection for Cesarean Section or Vaginal Delivery

K. Hsiao, M. Jeng, W. Soong, 1997, Clinical pediatrics.

Neonatal screening for glucose-6-phosphate dehydrogenase deficiency in Taiwan.

S. Chiang, S. J. Wu, K. Hsiao, 1999, The Southeast Asian journal of tropical medicine and public health.

Mutation Profile of the MUT Gene in Chinese Methylmalonic Aciduria Patients.

K. Hsiao, Y. Qi, Shio‐Jean Lin, 2012, JIMD reports.

Long-term neurodevelopmental outcomes of significant neonatal jaundice in Taiwan from 2000–2003: a nationwide, population-based cohort study

K. Hsiao, P. Chiang, M. Jeng, 2020, Scientific Reports.

The mutation spectrum of the phenylalanine hydroxylase (PAH) gene and associated haplotypes reveal ethnic heterogeneity in the Taiwanese population

K. Hsiao, Ying Liang, D. Niu, 2014, Journal of Human Genetics.

Comparing Strategies for Critical Congenital Heart Disease Newborn Screening.

K. Hsiao, M. Jeng, Pei-Chen Tsao, 2023, Pediatrics.

Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuria

K. Hsiao, Y. Qi, Shuan-Pei Lin, 2010, Journal of Human Genetics.

Identification of three novel 6‐pyruvoyl‐tetrahydropterin synthase gene mutations (226C>T, IVS3+1G>A, 116‐119delTGTT) in Chinese hyperphenylalaninemia caused by tetrahydrobiopterin synthesis deficiency

K. Hsiao, Tze-tze Liu, Yanling Yang, 2001, Human mutation.