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Journal of the Formosan Medical Association = Taiwan Yi Zhi|July 27, 2010
Self-efficacy affects blood sugar control among adolescents with type I diabetes mellitusAn-Hsuan Chih, Chyi-Feng Jan, San-Ging Shu, et al.Journal of the Formosan Medical Association = Taiwan Yi Zhi|December 24, 2003
Type I glutaric aciduria: phenotypes and genotypes in 5 Taiwanese childrenSan Ging Shu, Chi Ren Tsai, Liang Hui Chen, et al.Journal of the Formosan Medical Association = Taiwan Yi Zhi|June 26, 2007
Anthropometric and intellectual evaluation of individuals with Prader-Willi syndromeSan-Ging Shu, Shu Chien, Yen-Ching Wu, et al.Journal of the Formosan Medical Association = Taiwan Yi Zhi|September 14, 2004
A mucolipidosis III patient presenting characteristic sonographic and magnetic resonance imaging findings of claw hand deformityHsin-Hua Chen, Joung-Liang Lan, San-Ging Shu, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|September 10, 2009
High resolution melting analysis for mutation detection for PTPN11 gene: applications of this method for diagnosis of Noonan syndromeFu-Sung Lo, Ji-Dung Luo, Yann-Jinn Lee, et al.Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|February 28, 2003
Management of acute decompensation of neonatal maple syrup urine disease with continuous arteriovenous haemofiltration: report of one caseMing-Chih Lin, Chao-Huei Chen, Lin-Shien Fu, et al.Molecular Genetics and Metabolism|February 10, 2009
The gene founder effect of two spontaneous mutations in ethnic Chinese (Taiwanese) CAH patients with 21-hydroxylase deficiencyYann-Jinn Lee, Li-Ping Tsai, Dau-Ming Niu, et al.European Journal of Pediatrics|October 30, 2008
Noonan syndrome caused by germline KRAS mutation in Taiwan: report of two patients and a review of the literatureFu-Sung Lo, Ju-Li Lin, Min-Tzu Kuo, et al.Journal of the Formosan Medical Association = Taiwan Yi Zhi|July 23, 2003
Detection of novel CFTR mutations in Taiwanese cystic fibrosis patientsOzgül M Alper, San-Ging Shu, Mei-Hui Lee, et al.European Journal of Human Genetics : EJHG|September 26, 2003
Maple syrup urine disease in the Austronesian aboriginal tribe Paiwan of Taiwan: a novel DBT (E2) gene 4.7 kb founder deletion caused by a nonhomologous recombination between LINE-1 and Alu and the carrier-frequency determinationChing-Shiang Chi, Chi-Ren Tsai, Liang-Hui Chen, et al.Pageof 3