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Journal of Personalized Medicine
|
July 27, 2022
Surgical Strategy to Decrease the Revision Rate of Fassier-Duval Nailing in the Lower Limbs of Osteogenesis Imperfecta
Yi-Chi Hung, Kai-Yuan Cheng, Hsiang-Yu Lin, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi
|
June 28, 2008
Non-ketotic hyperglycinemia with a novel GLDC mutation in a Taiwanese child
Chia-Ying Chang, Shuan-Pei Lin, Hsiang-Yu Lin, et al.
Journal of Microbiology, Immunology, and Infection = Wei Mian Yu Gan Ran Za Zhi
|
June 30, 2005
A seroepidemiologic study of Helicobacter pylori and hepatitis A virus infection in primary school students in Taipei
Hsiang-Yu Lin, Chih-Kuang Chuang, Hung-Chang Lee, et al.
Orphanet Journal of Rare Diseases
|
September 3, 2014
A modified liquid chromatography/tandem mass spectrometry method for predominant disaccharide units of urinary glycosaminoglycans in patients with mucopolysaccharidoses
Chih-Kuang Chuang, Hsiang-Yu Lin, Tuen-Jen Wang, et al.
International Journal of Medical Sciences
|
February 2, 2021
Incidence and treatment of adult femoral fractures with osteogenesis imperfecta: An analysis of a center of 72 patients in Taiwan
Chung-Lin Lee, Shih-Chia Liu, Chen-Yu Yang, et al.
Pediatrics and Neonatology
|
November 20, 2019
Therapeutic strategy of patent ductus arteriosus in extremely preterm infants
Bai-Horng Su, Hsiang-Yu Lin, Hsiao-Yu Chiu, et al.
The Annals of Otology, Rhinology, and Laryngology
|
July 20, 2021
Airway Management of the Deformed Trachea Using T-Tube Stents in Patients with Mucopolysaccharidosis Type IVA
Yi-Hao Lee, Li-Chun Hsieh, Chin-Hui Su, et al.
Human Genetics
|
January 29, 2010
Novel human pathological mutations. Gene symbol: GLA. Disease: Fabry disease
Hsiang-Yu Lin, Kah-Wai Chong, Ju-Hui Hsu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 17, 2006
Detection of Hunter syndrome (mucopolysaccharidosis type II) in Taiwanese: biochemical and linkage studies of the iduronate-2-sulfatase gene defects in MPS II patients and carriers
Shuan-Pei Lin, Jui-Hung Chang, Guey-Jen Lee-Chen, et al.
JIMD Reports
|
March 13, 2015
Age at First Cardiac Symptoms in Fabry Disease: Association with a Chinese Hotspot Fabry Mutation (IVS4+919G>A), Classical Fabry Mutations, and Sex in a Taiwanese Population from the Fabry Outcome Survey (FOS)
Hao-Chuan Liu, Amandine Perrin, Ting-Rong Hsu, et al.
Page
of 19
Search research articles
Search
Showing results (41-50 of 183) with videos related to
Sort By:
Page
of 19
Journal of Personalized Medicine
|
July 27, 2022
Surgical Strategy to Decrease the Revision Rate of Fassier-Duval Nailing in the Lower Limbs of Osteogenesis Imperfecta
Yi-Chi Hung, Kai-Yuan Cheng, Hsiang-Yu Lin, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi
|
June 28, 2008
Non-ketotic hyperglycinemia with a novel GLDC mutation in a Taiwanese child
Chia-Ying Chang, Shuan-Pei Lin, Hsiang-Yu Lin, et al.
Journal of Microbiology, Immunology, and Infection = Wei Mian Yu Gan Ran Za Zhi
|
June 30, 2005
A seroepidemiologic study of Helicobacter pylori and hepatitis A virus infection in primary school students in Taipei
Hsiang-Yu Lin, Chih-Kuang Chuang, Hung-Chang Lee, et al.
Orphanet Journal of Rare Diseases
|
September 3, 2014
A modified liquid chromatography/tandem mass spectrometry method for predominant disaccharide units of urinary glycosaminoglycans in patients with mucopolysaccharidoses
Chih-Kuang Chuang, Hsiang-Yu Lin, Tuen-Jen Wang, et al.
International Journal of Medical Sciences
|
February 2, 2021
Incidence and treatment of adult femoral fractures with osteogenesis imperfecta: An analysis of a center of 72 patients in Taiwan
Chung-Lin Lee, Shih-Chia Liu, Chen-Yu Yang, et al.
Pediatrics and Neonatology
|
November 20, 2019
Therapeutic strategy of patent ductus arteriosus in extremely preterm infants
Bai-Horng Su, Hsiang-Yu Lin, Hsiao-Yu Chiu, et al.
The Annals of Otology, Rhinology, and Laryngology
|
July 20, 2021
Airway Management of the Deformed Trachea Using T-Tube Stents in Patients with Mucopolysaccharidosis Type IVA
Yi-Hao Lee, Li-Chun Hsieh, Chin-Hui Su, et al.
Human Genetics
|
January 29, 2010
Novel human pathological mutations. Gene symbol: GLA. Disease: Fabry disease
Hsiang-Yu Lin, Kah-Wai Chong, Ju-Hui Hsu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 17, 2006
Detection of Hunter syndrome (mucopolysaccharidosis type II) in Taiwanese: biochemical and linkage studies of the iduronate-2-sulfatase gene defects in MPS II patients and carriers
Shuan-Pei Lin, Jui-Hung Chang, Guey-Jen Lee-Chen, et al.
JIMD Reports
|
March 13, 2015
Age at First Cardiac Symptoms in Fabry Disease: Association with a Chinese Hotspot Fabry Mutation (IVS4+919G>A), Classical Fabry Mutations, and Sex in a Taiwanese Population from the Fabry Outcome Survey (FOS)
Hao-Chuan Liu, Amandine Perrin, Ting-Rong Hsu, et al.
Page
of 19