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Hsiang-Yu Lin

Showing results (31-40 of 183) with videos related to

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Hu Li Za Zhi the Journal of Nursing|February 3, 2017
[Using an Indicator-Based Reminder of Catheter Removal to Effectively Decrease Catheter-Associated Urinary Tract Infections in General Medical Patients]Pey-Tsung Wang, Hsiang-Yu Lin, Yi-Tsun Lin, et al.
Pediatrics and Neonatology|June 28, 2011
Efficacy of creamatocrit technique in evaluation of premature infants fed with breast milkHsiang-Yu Lin, Hsin-Yang Hsieh, Hung-Hsin Chen, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|November 29, 2011
Assessment of body composition using bioelectrical impedance analysis in Prader-Willi syndromeHsiang-Yu Lin, Ming-Ren Chen, Chih-Kuang Chuang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|July 10, 2009
Clinical features of osteogenesis imperfecta in TaiwanHsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang, et al.
Human Genetics|January 29, 2010
Novel human pathological mutations. Gene symbol: GLA. Disease: Fabry diseaseDau-Ming Niu, Hsiang-Yu Lin, Kah-Wai Chong, et al.
Pediatrics and Neonatology|March 24, 2020
Evidence base multi-discipline critical strategies toward better tomorrow for very preterm infantsHsiao-Yu Chiu, Shih-Ming Chu, Hsiang-Yu Lin, et al.
Orphanet Journal of Rare Diseases|May 14, 2013
Assessment of bone mineral density by dual energy x-ray absorptiometry in patients with mucopolysaccharidosesHsiang-Yu Lin, Shou-Chuan Shih, Chih-Kuang Chuang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|January 9, 2009
X-linked myotubular myopathy with a novel MTM1 mutation in a Taiwanese childChia-Ying Chang, Shuan-Pei Lin, Hsiang-Yu Lin, et al.
Human Genetics|January 29, 2010
Novel human pathological mutations. Gene symbol: GLA. Disease: Fabry diseaseHsiang-Yu Lin, Dau-Ming Niu, Kah-Wai Chong, et al.
International Journal of Neonatal Screening|September 22, 2025
Novel Phenotypic Insights into the <i>IDS</i> c.817C>T Variant in Mucopolysaccharidosis Type II from Newborn Screening CohortsÉliane Beauregard-Lacroix, Caitlin Menello, Madeline Steffensen, et al.
Pageof 19

Showing results (31-40 of 183) with videos related to

Sort By:
Pageof 19
Hu Li Za Zhi the Journal of Nursing|February 3, 2017
[Using an Indicator-Based Reminder of Catheter Removal to Effectively Decrease Catheter-Associated Urinary Tract Infections in General Medical Patients]Pey-Tsung Wang, Hsiang-Yu Lin, Yi-Tsun Lin, et al.
Pediatrics and Neonatology|June 28, 2011
Efficacy of creamatocrit technique in evaluation of premature infants fed with breast milkHsiang-Yu Lin, Hsin-Yang Hsieh, Hung-Hsin Chen, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|November 29, 2011
Assessment of body composition using bioelectrical impedance analysis in Prader-Willi syndromeHsiang-Yu Lin, Ming-Ren Chen, Chih-Kuang Chuang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|July 10, 2009
Clinical features of osteogenesis imperfecta in TaiwanHsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang, et al.
Human Genetics|January 29, 2010
Novel human pathological mutations. Gene symbol: GLA. Disease: Fabry diseaseDau-Ming Niu, Hsiang-Yu Lin, Kah-Wai Chong, et al.
Pediatrics and Neonatology|March 24, 2020
Evidence base multi-discipline critical strategies toward better tomorrow for very preterm infantsHsiao-Yu Chiu, Shih-Ming Chu, Hsiang-Yu Lin, et al.
Orphanet Journal of Rare Diseases|May 14, 2013
Assessment of bone mineral density by dual energy x-ray absorptiometry in patients with mucopolysaccharidosesHsiang-Yu Lin, Shou-Chuan Shih, Chih-Kuang Chuang, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|January 9, 2009
X-linked myotubular myopathy with a novel MTM1 mutation in a Taiwanese childChia-Ying Chang, Shuan-Pei Lin, Hsiang-Yu Lin, et al.
Human Genetics|January 29, 2010
Novel human pathological mutations. Gene symbol: GLA. Disease: Fabry diseaseHsiang-Yu Lin, Dau-Ming Niu, Kah-Wai Chong, et al.
International Journal of Neonatal Screening|September 22, 2025
Novel Phenotypic Insights into the <i>IDS</i> c.817C>T Variant in Mucopolysaccharidosis Type II from Newborn Screening CohortsÉliane Beauregard-Lacroix, Caitlin Menello, Madeline Steffensen, et al.
Pageof 19