Search research articles
Contact Us
Filters
Showing results (61-70 of 184) with videos related to
Page
of 19
Sort By:
Journal of the Chinese Medical Association : JCMA
|
March 26, 2021
Aortic regurgitation in Marfan syndrome patients who underwent prophylactic surgery: A single-center experience
Wen-Po Fan, Hsing-Yuan Li, Szu-Yin Tseng, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 3, 2024
Cardiomyocyte Globotriaosylceramide Accumulation in Adult Male Patients with Fabry Disease and IVS4 + 919G>A GLA Mutation is Progressive with Age and Correlates with Left Ventricular Hypertrophy and Reduced Left Ventricular Ejection Fraction
Fu-Pang Chang, Ting-Rong Hsu, Sheng-Che Hung, et al.
European Neurology
|
May 26, 2004
Congenital insensitivity to pain with anhidrosis in Taiwan: a morphometric and genetic study
Yuh-Cherng Guo, Kwong-Kum Liao, Bing-Wen Soong, et al.
Developmental Medicine and Child Neurology
|
September 3, 2015
Functional independence of Taiwanese children with Down syndrome
Hsiang-Yu Lin, Chih-Kuang Chuang, Yen-Jiun Chen, et al.
Orphanet Journal of Rare Diseases
|
December 3, 2015
Genotype and phenotype analysis of Taiwanese patients with osteogenesis imperfecta
Hsiang-Yu Lin, Chih-Kuang Chuang, Yi-Ning Su, et al.
Journal of the Endocrine Society
|
May 25, 2026
Genotype-phenotype correlation of biallelic DUOX2 mutations in transient and permanent congenital hypothyroidism
Sheng-Bin Liang, Chih-Ya Cheng, Yun-Ru Chen, et al.
Molecular Genetics and Metabolism
|
March 12, 2014
High-throughput detection of common sequence variations of Fabry disease in Taiwan using DNA mass spectrometry
Sheng-Hung Lee, Cheng-Fang Li, Hsiang-Yu Lin, et al.
Journal of Clinical Lipidology
|
April 26, 2015
Clinical observations and treatment of pediatric homozygous familial hypercholesterolemia due to a low-density lipoprotein receptor defect
Cheng-Hung Huang, Pao-Chin Chiu, Hao-Chuan Liu, et al.
American Journal of Medical Genetics. Part A
|
January 19, 2020
Airway abnormalities in very early treated infantile-onset Pompe disease: A large-scale survey by flexible bronchoscopy
Chia-Feng Yang, Dau-Ming Niu, Shyh-Kuan Tai, et al.
Orphanet Journal of Rare Diseases
|
August 31, 2018
Cardiac features and effects of enzyme replacement therapy in Taiwanese patients with Mucopolysaccharidosis IVA
Hsiang-Yu Lin, Ming-Ren Chen, Shan-Miao Lin, et al.
Page
of 19
Search research articles
Search
Showing results (61-70 of 184) with videos related to
Sort By:
Page
of 19
Journal of the Chinese Medical Association : JCMA
|
March 26, 2021
Aortic regurgitation in Marfan syndrome patients who underwent prophylactic surgery: A single-center experience
Wen-Po Fan, Hsing-Yuan Li, Szu-Yin Tseng, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 3, 2024
Cardiomyocyte Globotriaosylceramide Accumulation in Adult Male Patients with Fabry Disease and IVS4 + 919G>A GLA Mutation is Progressive with Age and Correlates with Left Ventricular Hypertrophy and Reduced Left Ventricular Ejection Fraction
Fu-Pang Chang, Ting-Rong Hsu, Sheng-Che Hung, et al.
European Neurology
|
May 26, 2004
Congenital insensitivity to pain with anhidrosis in Taiwan: a morphometric and genetic study
Yuh-Cherng Guo, Kwong-Kum Liao, Bing-Wen Soong, et al.
Developmental Medicine and Child Neurology
|
September 3, 2015
Functional independence of Taiwanese children with Down syndrome
Hsiang-Yu Lin, Chih-Kuang Chuang, Yen-Jiun Chen, et al.
Orphanet Journal of Rare Diseases
|
December 3, 2015
Genotype and phenotype analysis of Taiwanese patients with osteogenesis imperfecta
Hsiang-Yu Lin, Chih-Kuang Chuang, Yi-Ning Su, et al.
Journal of the Endocrine Society
|
May 25, 2026
Genotype-phenotype correlation of biallelic DUOX2 mutations in transient and permanent congenital hypothyroidism
Sheng-Bin Liang, Chih-Ya Cheng, Yun-Ru Chen, et al.
Molecular Genetics and Metabolism
|
March 12, 2014
High-throughput detection of common sequence variations of Fabry disease in Taiwan using DNA mass spectrometry
Sheng-Hung Lee, Cheng-Fang Li, Hsiang-Yu Lin, et al.
Journal of Clinical Lipidology
|
April 26, 2015
Clinical observations and treatment of pediatric homozygous familial hypercholesterolemia due to a low-density lipoprotein receptor defect
Cheng-Hung Huang, Pao-Chin Chiu, Hao-Chuan Liu, et al.
American Journal of Medical Genetics. Part A
|
January 19, 2020
Airway abnormalities in very early treated infantile-onset Pompe disease: A large-scale survey by flexible bronchoscopy
Chia-Feng Yang, Dau-Ming Niu, Shyh-Kuan Tai, et al.
Orphanet Journal of Rare Diseases
|
August 31, 2018
Cardiac features and effects of enzyme replacement therapy in Taiwanese patients with Mucopolysaccharidosis IVA
Hsiang-Yu Lin, Ming-Ren Chen, Shan-Miao Lin, et al.
Page
of 19