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Diagnostics (Basel, Switzerland)
|
January 26, 2020
Cardiac Evaluation using Two-Dimensional Speckle-Tracking Echocardiography and Conventional Echocardiography in Taiwanese Patients with Mucopolysaccharidoses
Hsiang-Yu Lin, Chih-Kuang Chuang, Chung-Lin Lee, et al.
The Canadian Journal of Cardiology
|
February 28, 2016
Evaluation of Proinflammatory Prognostic Biomarkers for Fabry Cardiomyopathy With Enzyme Replacement Therapy
Kuan-Hsuan Chen, Yueh Chien, Kang-Ling Wang, et al.
Orphanet Journal of Rare Diseases
|
June 20, 2022
Twenty years of the Fabry Outcome Survey (FOS): insights, achievements, and lessons learned from a global patient registry
Michael Beck, Uma Ramaswami, Elizabeth Hernberg-Ståhl, et al.
American Journal of Medical Genetics. Part A
|
April 28, 2009
Incidence of the mucopolysaccharidoses in Taiwan, 1984-2004
Hsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang, et al.
Orphanet Journal of Rare Diseases
|
July 23, 2014
Globotriaosylsphingosine (lyso-Gb3) might not be a reliable marker for monitoring the long-term therapeutic outcomes of enzyme replacement therapy for late-onset Fabry patients with the Chinese hotspot mutation (IVS4+919G>A)
Hao-Chuan Liu, Hsiang-Yu Lin, Chia-Feng Yang, et al.
The Journal of Pediatrics
|
December 20, 2015
Very Early Treatment for Infantile-Onset Pompe Disease Contributes to Better Outcomes
Chia-Feng Yang, Chen Chang Yang, Hsuan-Chieh Liao, et al.
Clinical Kidney Journal
|
January 4, 2021
Fabry disease and COVID-19: international expert recommendations for management based on real-world experience
Dawn A Laney, Dominique P Germain, João Paulo Oliveira, et al.
Pediatric Transplantation
|
January 17, 2022
Safety and long-term outcomes of early liver transplantation for pediatric methylmalonic acidemia patients
Niang-Cheng Lin, Hsin-Lin Tsai, Cheng-Yen Chen, et al.
Diagnostics (Basel, Switzerland)
|
October 9, 2019
An At-Risk Population Screening Program for Mucopolysaccharidoses by Measuring Urinary Glycosaminoglycans in Taiwan
Hsiang-Yu Lin, Chung-Lin Lee, Yun-Ting Lo, et al.
American Journal of Medical Genetics. Part A
|
November 19, 2013
A large-scale nationwide newborn screening program for Pompe disease in Taiwan: towards effective diagnosis and treatment
Chia-Feng Yang, Hao-Chuan Liu, Ting-Rong Hsu, et al.
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Search research articles
Search
Showing results (131-140 of 184) with videos related to
Sort By:
Page
of 19
Diagnostics (Basel, Switzerland)
|
January 26, 2020
Cardiac Evaluation using Two-Dimensional Speckle-Tracking Echocardiography and Conventional Echocardiography in Taiwanese Patients with Mucopolysaccharidoses
Hsiang-Yu Lin, Chih-Kuang Chuang, Chung-Lin Lee, et al.
The Canadian Journal of Cardiology
|
February 28, 2016
Evaluation of Proinflammatory Prognostic Biomarkers for Fabry Cardiomyopathy With Enzyme Replacement Therapy
Kuan-Hsuan Chen, Yueh Chien, Kang-Ling Wang, et al.
Orphanet Journal of Rare Diseases
|
June 20, 2022
Twenty years of the Fabry Outcome Survey (FOS): insights, achievements, and lessons learned from a global patient registry
Michael Beck, Uma Ramaswami, Elizabeth Hernberg-Ståhl, et al.
American Journal of Medical Genetics. Part A
|
April 28, 2009
Incidence of the mucopolysaccharidoses in Taiwan, 1984-2004
Hsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang, et al.
Orphanet Journal of Rare Diseases
|
July 23, 2014
Globotriaosylsphingosine (lyso-Gb3) might not be a reliable marker for monitoring the long-term therapeutic outcomes of enzyme replacement therapy for late-onset Fabry patients with the Chinese hotspot mutation (IVS4+919G>A)
Hao-Chuan Liu, Hsiang-Yu Lin, Chia-Feng Yang, et al.
The Journal of Pediatrics
|
December 20, 2015
Very Early Treatment for Infantile-Onset Pompe Disease Contributes to Better Outcomes
Chia-Feng Yang, Chen Chang Yang, Hsuan-Chieh Liao, et al.
Clinical Kidney Journal
|
January 4, 2021
Fabry disease and COVID-19: international expert recommendations for management based on real-world experience
Dawn A Laney, Dominique P Germain, João Paulo Oliveira, et al.
Pediatric Transplantation
|
January 17, 2022
Safety and long-term outcomes of early liver transplantation for pediatric methylmalonic acidemia patients
Niang-Cheng Lin, Hsin-Lin Tsai, Cheng-Yen Chen, et al.
Diagnostics (Basel, Switzerland)
|
October 9, 2019
An At-Risk Population Screening Program for Mucopolysaccharidoses by Measuring Urinary Glycosaminoglycans in Taiwan
Hsiang-Yu Lin, Chung-Lin Lee, Yun-Ting Lo, et al.
American Journal of Medical Genetics. Part A
|
November 19, 2013
A large-scale nationwide newborn screening program for Pompe disease in Taiwan: towards effective diagnosis and treatment
Chia-Feng Yang, Hao-Chuan Liu, Ting-Rong Hsu, et al.
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of 19