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Journal of Personalized Medicine
|
August 26, 2022
The Anesthetic Strategy for Patients with Mucopolysaccharidoses: A Retrospective Cohort Study
Hsuan-Chih Lao, Ying-Chun Lin, Muh-Lii Liang, et al.
Journal of Personalized Medicine
|
May 28, 2022
Long-Term Cardiovascular Findings in Williams Syndrome: A Single Medical Center Experience in Taiwan
Chung-Lin Lee, Shan-Miao Lin, Ming-Ren Chen, et al.
Diagnostics (Basel, Switzerland)
|
October 17, 2019
Relationships among Height, Weight, Body Mass Index, and Age in Taiwanese Children with Different Types of Mucopolysaccharidoses
Hsiang-Yu Lin, Chung-Lin Lee, Pao Chin Chiu, et al.
American Journal of Medical Genetics. Part A
|
May 14, 2011
A novel mutation in PYCR1 causes an autosomal recessive cutis laxa with premature aging features in a family
Dar-Shong Lin, Chun-Yan Yeung, Hsuan-Liang Liu, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
June 1, 2007
Genotype and phenotype in patients with Prader-Willi syndrome in Taiwan
Hsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang, et al.
Diagnostics (Basel, Switzerland)
|
May 1, 2025
Systematic Analysis of Multiple Imaging Modalities in Infants Diagnosed with Mucopolysaccharidosis by Newborn Screening
Chung-Lin Lee, Szu-Wen Chang, Hung-Hsiang Fang, et al.
Molecular Genetics & Genomic Medicine
|
March 9, 2019
Ophthalmologic manifestations in Taiwanese patients with mucopolysaccharidoses
Hsiang-Yu Lin, Wei-Chun Chan, Lee-Jen Chen, et al.
American Journal of Medical Genetics. Part A
|
November 21, 2012
Functional independence of Taiwanese children with VACTERL association
Hsin-Yi Lin, Shuan-Pei Lin, Hsiang-Yu Lin, et al.
Orphanet Journal of Rare Diseases
|
December 19, 2018
Galloway-Mowat syndrome in Taiwan: OSGEP mutation and unique clinical phenotype
Pei-Yi Lin, Min-Hua Tseng, Martin Zenker, et al.
Orphanet Journal of Rare Diseases
|
June 6, 2018
Clinical characteristics and surgical history of Taiwanese patients with mucopolysaccharidosis type II: data from the hunter outcome survey (HOS)
Hsiang-Yu Lin, Chih-Kuang Chuang, Ming-Ren Chen, et al.
Page
of 29
Search research articles
Search
Showing results (201-210 of 281) with videos related to
Sort By:
Page
of 29
Journal of Personalized Medicine
|
August 26, 2022
The Anesthetic Strategy for Patients with Mucopolysaccharidoses: A Retrospective Cohort Study
Hsuan-Chih Lao, Ying-Chun Lin, Muh-Lii Liang, et al.
Journal of Personalized Medicine
|
May 28, 2022
Long-Term Cardiovascular Findings in Williams Syndrome: A Single Medical Center Experience in Taiwan
Chung-Lin Lee, Shan-Miao Lin, Ming-Ren Chen, et al.
Diagnostics (Basel, Switzerland)
|
October 17, 2019
Relationships among Height, Weight, Body Mass Index, and Age in Taiwanese Children with Different Types of Mucopolysaccharidoses
Hsiang-Yu Lin, Chung-Lin Lee, Pao Chin Chiu, et al.
American Journal of Medical Genetics. Part A
|
May 14, 2011
A novel mutation in PYCR1 causes an autosomal recessive cutis laxa with premature aging features in a family
Dar-Shong Lin, Chun-Yan Yeung, Hsuan-Liang Liu, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
June 1, 2007
Genotype and phenotype in patients with Prader-Willi syndrome in Taiwan
Hsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang, et al.
Diagnostics (Basel, Switzerland)
|
May 1, 2025
Systematic Analysis of Multiple Imaging Modalities in Infants Diagnosed with Mucopolysaccharidosis by Newborn Screening
Chung-Lin Lee, Szu-Wen Chang, Hung-Hsiang Fang, et al.
Molecular Genetics & Genomic Medicine
|
March 9, 2019
Ophthalmologic manifestations in Taiwanese patients with mucopolysaccharidoses
Hsiang-Yu Lin, Wei-Chun Chan, Lee-Jen Chen, et al.
American Journal of Medical Genetics. Part A
|
November 21, 2012
Functional independence of Taiwanese children with VACTERL association
Hsin-Yi Lin, Shuan-Pei Lin, Hsiang-Yu Lin, et al.
Orphanet Journal of Rare Diseases
|
December 19, 2018
Galloway-Mowat syndrome in Taiwan: OSGEP mutation and unique clinical phenotype
Pei-Yi Lin, Min-Hua Tseng, Martin Zenker, et al.
Orphanet Journal of Rare Diseases
|
June 6, 2018
Clinical characteristics and surgical history of Taiwanese patients with mucopolysaccharidosis type II: data from the hunter outcome survey (HOS)
Hsiang-Yu Lin, Chih-Kuang Chuang, Ming-Ren Chen, et al.
Page
of 29