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

Hsiang-Yu Lin

Showing results (61-70 of 183) with videos related to

Pageof 19
Sort By:
Journal of Neonatal-Perinatal Medicine|April 11, 2022
Epidemiological evolution of early-onset neonatal sepsis over 12 years: A single center, population-based study in central TaiwanI-Chun Lu, Yu-Chia Chang, Yin-Ting 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.
Diagnostics (Basel, Switzerland)|October 24, 2020
Effect of Mutated <i>ids</i> Overexpression on IDS Enzyme Activity and Developmental Phenotypes in Zebrafish Embryos: A Valuable Index for Assessing Critical Point-Mutations Associated with Mucopolysaccharidosis Type II Occurrence in HumansCheng-Yung Lin, Hsiang-Yu Lin, Chih-Kuang Chuang, et al.
Journal of Personalized Medicine|July 27, 2022
Quantification of Idua Enzymatic Activity Combined with Observation of Phenotypic Change in Zebrafish Embryos Provide a Preliminary Assessment of Mutated <i>idua</i> Correlated with Mucopolysaccharidosis Type ICheng-Yung Lin, Hsiang-Yu Lin, Chih-Kuang Chuang, et al.
Journal of Personalized Medicine|July 27, 2022
Functional Independence of Taiwanese Children with Osteogenesis ImperfectaYu-Min Syu, Chung-Lin Lee, Chih-Kuang Chuang, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: GAA. Disease: glycogen storage disease 2Hsiang-Yu Lin, Tina Jui-Ting Wu, Ju-Hui Hsu, et al.
Archives of Dermatological Research|April 7, 2007
Netherton syndrome: mutation analysis of two Taiwanese familiesShuan-Pei Lin, Shu-Yi Huang, Mei-Eng Tu, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 19, 2021
Detection of hypermethylation at H19DMR at amniocentesis in a fetus with overgrowth, distended abdomen and Beckwith-Wiedemann syndromeChih-Ping Chen, Schu-Rern Chern, Chien-Hsing Lin, et al.
Journal of Clinical Ultrasound : JCU|March 22, 2007
Prenatal sonographic findings of Klippel-Trénaunay-Weber syndromeChih-Ping Chen, Shuan-Pei Lin, Tung-Yao Chang, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|April 29, 2008
Cri-du-chat syndromeChia-Ying Chang, Shuan-Pei Lin, Hsiang-Yu Lin, et al.
Pageof 19

Showing results (61-70 of 183) with videos related to

Sort By:
Pageof 19
Journal of Neonatal-Perinatal Medicine|April 11, 2022
Epidemiological evolution of early-onset neonatal sepsis over 12 years: A single center, population-based study in central TaiwanI-Chun Lu, Yu-Chia Chang, Yin-Ting 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.
Diagnostics (Basel, Switzerland)|October 24, 2020
Effect of Mutated <i>ids</i> Overexpression on IDS Enzyme Activity and Developmental Phenotypes in Zebrafish Embryos: A Valuable Index for Assessing Critical Point-Mutations Associated with Mucopolysaccharidosis Type II Occurrence in HumansCheng-Yung Lin, Hsiang-Yu Lin, Chih-Kuang Chuang, et al.
Journal of Personalized Medicine|July 27, 2022
Quantification of Idua Enzymatic Activity Combined with Observation of Phenotypic Change in Zebrafish Embryos Provide a Preliminary Assessment of Mutated <i>idua</i> Correlated with Mucopolysaccharidosis Type ICheng-Yung Lin, Hsiang-Yu Lin, Chih-Kuang Chuang, et al.
Journal of Personalized Medicine|July 27, 2022
Functional Independence of Taiwanese Children with Osteogenesis ImperfectaYu-Min Syu, Chung-Lin Lee, Chih-Kuang Chuang, et al.
Human Genetics|April 14, 2011
Novel human pathological mutations. Gene symbol: GAA. Disease: glycogen storage disease 2Hsiang-Yu Lin, Tina Jui-Ting Wu, Ju-Hui Hsu, et al.
Archives of Dermatological Research|April 7, 2007
Netherton syndrome: mutation analysis of two Taiwanese familiesShuan-Pei Lin, Shu-Yi Huang, Mei-Eng Tu, et al.
Taiwanese Journal of Obstetrics & Gynecology|November 19, 2021
Detection of hypermethylation at H19DMR at amniocentesis in a fetus with overgrowth, distended abdomen and Beckwith-Wiedemann syndromeChih-Ping Chen, Schu-Rern Chern, Chien-Hsing Lin, et al.
Journal of Clinical Ultrasound : JCU|March 22, 2007
Prenatal sonographic findings of Klippel-Trénaunay-Weber syndromeChih-Ping Chen, Shuan-Pei Lin, Tung-Yao Chang, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|April 29, 2008
Cri-du-chat syndromeChia-Ying Chang, Shuan-Pei Lin, Hsiang-Yu Lin, et al.
Pageof 19