Search research articles
Contact Us
Filters
Showing results (151-160 of 184) with videos related to
Page
of 19
Sort By:
Journal of Inherited Metabolic Disease
|
October 7, 2010
Enzyme replacement therapy for mucopolysaccharidosis VI--experience in Taiwan
Hsiang-Yu Lin, Ming-Ren Chen, Chih-Kuang Chuang, et al.
American Journal of Medical Genetics. Part A
|
August 3, 2018
Mucopolysaccharidosis III in Taiwan: Natural history, clinical and molecular characteristics of 28 patients diagnosed during a 21-year period
Hsiang-Yu Lin, Chih-Kuang Chuang, Chung-Lin Lee, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 12, 2014
Detecting multiple lysosomal storage diseases by tandem mass spectrometry--a national newborn screening program in Taiwan
Hsuan-Chieh Liao, Chuan-Chi Chiang, Dau-Ming Niu, et al.
Journal of Human Genetics
|
January 13, 2012
Mutation spectrum of and founder effects affecting the PTS gene in East Asian populations
Yen-Hui Chiu, Ying-Chen Chang, Yu-Hsin Chang, et al.
Journal of Human Genetics
|
December 8, 2017
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
Yung-Hsiu Lu, Po-Hsun Huang, Li-Yun Wang, et al.
JIMD Reports
|
February 23, 2013
Mutation Profile of the MUT Gene in Chinese Methylmalonic Aciduria Patients
Mei-Ying Liu, Tze-Tze Liu, Yang-Ling Yang, et al.
Journal of Personalized Medicine
|
July 27, 2022
Newborn Screening Program for Mucopolysaccharidosis Type II and Long-Term Follow-Up of the Screen-Positive Subjects in Taiwan
Hsiang-Yu Lin, Ya-Hui Chang, Chung-Lin Lee, et al.
BMJ Open
|
July 19, 2013
Effects of enzyme replacement therapy for cardiac-type Fabry patients with a Chinese hotspot late-onset Fabry mutation (IVS4+919G>A)
Hsiang-Yu Lin, Hao-Chuan Liu, Yu-Hsiu Huang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 8, 2024
Implementation of newborn screening for mucopolysaccharidosis type IVA and long-term monitoring in Taiwan
Hsiang-Yu Lin, Chung-Lin Lee, Ya-Hui Chang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 9, 2011
The use of high resolution melting analysis to detect Fabry mutations in heterozygous females via dry bloodspots
Chang-Long Tai, Mei-Ying Liu, Hsiao-Chi Yu, et al.
Page
of 19
Search research articles
Search
Showing results (151-160 of 184) with videos related to
Sort By:
Page
of 19
Journal of Inherited Metabolic Disease
|
October 7, 2010
Enzyme replacement therapy for mucopolysaccharidosis VI--experience in Taiwan
Hsiang-Yu Lin, Ming-Ren Chen, Chih-Kuang Chuang, et al.
American Journal of Medical Genetics. Part A
|
August 3, 2018
Mucopolysaccharidosis III in Taiwan: Natural history, clinical and molecular characteristics of 28 patients diagnosed during a 21-year period
Hsiang-Yu Lin, Chih-Kuang Chuang, Chung-Lin Lee, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 12, 2014
Detecting multiple lysosomal storage diseases by tandem mass spectrometry--a national newborn screening program in Taiwan
Hsuan-Chieh Liao, Chuan-Chi Chiang, Dau-Ming Niu, et al.
Journal of Human Genetics
|
January 13, 2012
Mutation spectrum of and founder effects affecting the PTS gene in East Asian populations
Yen-Hui Chiu, Ying-Chen Chang, Yu-Hsin Chang, et al.
Journal of Human Genetics
|
December 8, 2017
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
Yung-Hsiu Lu, Po-Hsun Huang, Li-Yun Wang, et al.
JIMD Reports
|
February 23, 2013
Mutation Profile of the MUT Gene in Chinese Methylmalonic Aciduria Patients
Mei-Ying Liu, Tze-Tze Liu, Yang-Ling Yang, et al.
Journal of Personalized Medicine
|
July 27, 2022
Newborn Screening Program for Mucopolysaccharidosis Type II and Long-Term Follow-Up of the Screen-Positive Subjects in Taiwan
Hsiang-Yu Lin, Ya-Hui Chang, Chung-Lin Lee, et al.
BMJ Open
|
July 19, 2013
Effects of enzyme replacement therapy for cardiac-type Fabry patients with a Chinese hotspot late-onset Fabry mutation (IVS4+919G>A)
Hsiang-Yu Lin, Hao-Chuan Liu, Yu-Hsiu Huang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 8, 2024
Implementation of newborn screening for mucopolysaccharidosis type IVA and long-term monitoring in Taiwan
Hsiang-Yu Lin, Chung-Lin Lee, Ya-Hui Chang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 9, 2011
The use of high resolution melting analysis to detect Fabry mutations in heterozygous females via dry bloodspots
Chang-Long Tai, Mei-Ying Liu, Hsiao-Chi Yu, et al.
Page
of 19