English  |  正體中文  |  简体中文  |  Total items :2809390  
Visitors :  27001496    Online Users :  518
Project Commissioned by the Ministry of Education
Project Executed by National Taiwan University Library
 
臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
About TAIR

Browse By

News

Copyright

Related Links

"ng yy"

Return to Browse by Author
Sorting by Title Sort by Date

Showing items 1-14 of 14  (1 Page(s) Totally)
1 
View [10|25|50] records per page

Institution Date Title Author
國家衛生研究院 2021-11-17 The effectiveness of pay-for-performance program of diabetes care for psychiatric patients: A regional psychiatric hospital experience Yang, CC;Lan, TH;Tsai, WC;Guo, MC;Ng, YY;Wu, SC
中山醫學大學 2021 Proinflammatory Responses of 1-Nitropyrene against RAW264.7 Macrophages through Akt Phosphorylation and NF-kappa B Pathways Tsai, PK; Chen, SP; Huang-Liu, R; Chen, CJ; Chen, WY; Ng, YY; Kuan, YH
中山醫學大學 2021 3-Bromofluoranthene-induced cardiotoxicity of zebrafish and apoptosis in the vascular endothelial cells via intrinsic and extrinsic caspase-dependent pathways Su, CH; Chen, SP; Chen, LY; Yang, JJ; Lee, YC; Lee, SS; Chen, HH; Ng, YY; Kuan, YH
中山醫學大學 2012 Nine genes that may contribute to partial trisomy (6)(p22→pter) and unique presentation of persistent hyperplastic primary vitreous with retinal detachment. Su, PH; Lee, IC; Yang, SF; Ng, YY; Liu, CS; Chen, JY
中山醫學大學 2012 A MID1 gene mutation in a patient with Opitz G/BBB syndrome that altered the 3D structure of SPRY domain. Hu, CH; Liu, YF; Yu, JS; Ng, YY; Chen, SJ; Su, PH; Chen, JY
中山醫學大學 2012 Efficacy of intermediate-dose oral erythromycin on very low birth weight infants with feeding intolerance. Ng, YY; Su, PH; Chen, JY; Quek, YW; Hu, JM; Lee, IC; Lee, HS; Chang, HP
中山醫學大學 2012 Congenital myotubular myopathy with a novel MTM1 gene mutation in a premature infant presenting with ventilator dependency and intrahepatic cholestasis. Lee, IC; Su, PH; Chen, JY; Hu, JM; Lu, JJ; Ng, YY
中山醫學大學 2010-09 Associations of serum leptin with atopic asthma and allergic rhinitis in children. Quek YW; Sun HL; Ng YY; Lee HS; Yang SF; Ku MS; Lu KH; Sheu JN; Lue KH
臺北醫學大學 2008 Determinants of catheter loss following continuous ambulatory peritoneal dialysis peritonitis. 陳振文; Yang CY; Chen TW; Lin YP; Lin CC; Ng YY; Yang WC; Chen JY
中山醫學大學 2008 Trisomy 18 syndrome with incomplete Cantrell syndrome. Hou, YJ; Chen, FL; Ng, YY; Hu, JM; Chen, SJ; Chen, JY; Su, PH
中山醫學大學 2008 Hydranencephaly associated with interruption of bilateral internal carotid arteries. Quek, YW; Su, PH; Tsao, TF; Chen, JY; Ng, YY; Hu, JM; Chen, SJ
中山醫學大學 2006 Goldenhar syndrome (oculoauriculovertebral dysplasia): report of one case. Ng, YY; Hu, JM; Su, PH; Chen, JY; Yang, MS; Chen, SJ
臺北醫學大學 2005 Blockade of NFkappaB activation and renal inflammation by ultrasound-mediated gene transfer of Smad7 in rat remnant kidney 侯君正; Ng YY; Hou CC; Wang W; Huang XR; Lan HY;
臺北醫學大學 1998 Focal segmental glomerulosclerosis after poststreptococcal glomerulonephritis in the elderly: a case report. 許永和; Hsu YH; Ng YY; Yang AH; Chen TW; Huang TP.;

Showing items 1-14 of 14  (1 Page(s) Totally)
1 
View [10|25|50] records per page