Sheng-Kai Chang

发表

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.

Whole Exome Sequencing of Patients With Heritable and Idiopathic Pulmonary Arterial Hypertension in Central Taiwan

K. Liang, Kuo-Yang Wang, Wei-Wen Lin, 2022, Frontiers in Cardiovascular Medicine.

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.

Identification of lysosomal and extralysosomal globotriaosylceramide (Gb3) accumulations before the occurrence of typical pathological changes in the endomyocardial biopsies of Fabry disease patients

Wen-Chung Yu, Yen-Feng Wang, S. Hung, 2018, Genetics in Medicine.

The Fabry disease-causing mutation, GLA IVS4+919G>A, originated in Mainland China more than 800 years ago

Yun-Ru Chen, Kung-Hao Liang, D. Niu, 2020, Journal of Human Genetics.

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.

Audiological and otologic manifestations of glutaric aciduria type I

D. Niu, Yen-Fu Cheng, Chia-Hung Wu, 2020, Orphanet Journal of Rare Diseases.

Identification of lysosomal and extralysosomal globotriaosylceramide (Gb3) accumulations before the occurrence of typical pathological changes in the endomyocardial biopsies of Fabry disease patients

Wen-Chung Yu, Yen-Feng Wang, S. Hung, 2018, Genetics in Medicine.

A cluster of heritable pulmonary arterial hypertension cases in a family with all three siblings carrying the same novel AQP1 c.273C>G variant‐a case report

K. Liang, Yu-Wei Chen, W. Tsai, 2023, Pulmonary circulation.

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.