Hui-Chen Ho

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.

Fatty Acid oxidation disorders in a chinese population in taiwan.

Y. Chien, W. Hwu, M. Chao, 2013, JIMD reports.

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.

Status of newborn screening and follow up investigations for Mucopolysaccharidoses I and II in Taiwan

Hsiang-Yu Lin, Shuan-Pei Lin, C. Chuang, 2018, Orphanet Journal of Rare Diseases.

Later Onset Fabry Disease, Cardiac Damage Progress in Silence: Experience With a Highly Prevalent Mutation.

Wen-Chung Yu, R. Desnick, Hsiang-Yu Lin, 2016, Journal of the American College of Cardiology.

Very rare condition of multiple Gaucheroma: A case report and review of the literature

W. Soong, Y. Yeh, D. Niu, 2019, Molecular genetics and metabolism reports.

Spanning Connectivity of the WK-Recursive Networks

Lih-Hsing Hsu, C. R.O., Hui-Chen Ho, 2010 .

Very Early Treatment for Infantile-Onset Pompe Disease Contributes to Better Outcomes.

W. Soong, Chih-jou Lai, D. Niu, 2016, The Journal of pediatrics.

Improvement in the sensitivity of newborn screening for Fabry disease among females through the use of a high-throughput and cost-effective method, DNA mass spectrometry

S. Hung, Po‐Hsun Huang, D. Niu, 2017, Journal of Human Genetics.

A large‐scale nationwide newborn screening program for pompe disease in Taiwan: Towards effective diagnosis and treatment

Chih-jou Lai, D. Niu, Hui-Chen Ho, 2014, American journal of medical genetics. Part A.

Genotypic and phenotypic correlations of biotinidase deficiency in the Chinese population

Y. Chien, W. Hwu, Hui-Chen Ho, 2019, Orphanet Journal of Rare Diseases.

Improvement in the sensitivity of newborn screening for Fabry disease among females through the use of a high-throughput and cost-effective method, DNA mass spectrometry

S. Hung, Po‐Hsun Huang, D. Niu, 2017, Journal of Human Genetics.

Very rare condition of multiple Gaucheroma: A case report and review of the literature☆

W. Soong, Y. Yeh, D. Niu, 2019, Molecular genetics and metabolism reports.

Comparing Strategies for Critical Congenital Heart Disease Newborn Screening.

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

Long-term outcomes of very early treated infantile-onset Pompe disease with short-term steroid premedication: experiences from a nationwide newborn screening programme

D. Niu, S. Kao, Hui-Chen Ho, 2022, Journal of Medical Genetics.

Very Early Treatment for Infantile-Onset Pompe Disease Contributes to Better Outcomes.

W. Soong, Chih-jou Lai, D. Niu, 2016, The Journal of pediatrics.

Later Onset Fabry Disease, Cardiac Damage Progress in Silence: Experience With a Highly Prevalent Mutation.

Wen-Chung Yu, R. Desnick, Hsiang-Yu Lin, 2016, Journal of the American College of Cardiology.

Fatty Acid oxidation disorders in a chinese population in taiwan.

Y. Chien, W. Hwu, M. Chao, 2013, JIMD reports.