Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Dau-Ming Niu

Showing results (61-70 of 184) with videos related to

Pageof 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 experienceWen-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 FractionFu-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 studyYuh-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 syndromeHsiang-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 imperfectaHsiang-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 hypothyroidismSheng-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 spectrometrySheng-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 defectCheng-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 bronchoscopyChia-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 IVAHsiang-Yu Lin, Ming-Ren Chen, Shan-Miao Lin, et al.
Pageof 19

Showing results (61-70 of 184) with videos related to

Sort By:
Pageof 19
Journal of the Chinese Medical Association : JCMA|March 26, 2021
Aortic regurgitation in Marfan syndrome patients who underwent prophylactic surgery: A single-center experienceWen-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 FractionFu-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 studyYuh-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 syndromeHsiang-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 imperfectaHsiang-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 hypothyroidismSheng-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 spectrometrySheng-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 defectCheng-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 bronchoscopyChia-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 IVAHsiang-Yu Lin, Ming-Ren Chen, Shan-Miao Lin, et al.
Pageof 19