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Showing results 481 to 500 of 13340

Pub YearTitleAuthor(s)
2015A Dunnione Compound MB12662 Improves Cisplatin-Induced Tissue Injury and Emesis.박동선
2011A Factor of Fasting Blood Glucose and Dietary Patterns in Korean Adults Using Data From the 2007, 2008 and 2009 Korea National Health and Nutrition Examination Survey전기홍
1996A Familial Case Report of May-Hegglin Anomaly강원형, 임영애, 전희선
2008A Family Case of Complete Androgen Insensitivity Syndrome in Sisters due to a Novel Mutation in the Androgen Receptor Gene김미란, 김현주, 정윤석, 주희재
2011A fatal case of flufenoxuron-containing insecticide poisoning complicated by lactic acidosis, shock, abdominal compartment syndrome.민영기, 박은정, 최상천
2019A feasibility study of laparoscopic total gastrectomy for clinical stage I gastric cancer: a prospective multi-center phase II clinical trial, KLASS 03한상욱
2012A fibrous stromal component in hepatocellular carcinoma reveals a cholangiocarcinoma-like gene expression trait and epithelial-mesenchymal transition김영배, 우현구
2009A Floppy Baby with Congenital Myotonic Dystrophy Complicated with Huge Subgaleal Hematoma Occurring in Non-instrumental Vaginal Delivery이일영, 임신영
2015A focal marked hypoechogenicity within an isoechoic thyroid nodule: is it a focal malignancy or not?하은주
2019A formulated red ginseng extract inhibits autophagic flux and sensitizes to doxorubicin-induced cell death김유선
2013A formulated red ginseng extract upregulates CHOP and increases TRAIL-mediated cytotoxicity in human hepatocellular carcinoma cells.김유선
2011A founder mutation of CANT1 common in Korean and Japanese Desbuquois dysplasia.김옥화
2003A Four-year Follow-up Case of Oligomeganephronia Detected Early by School Screening Urinalysis-
2021A framework (SOCRATex) for hierarchical annotation of unstructured electronic health records and integration into a standardized medical database: Development and usability study노진, 박래웅, 정재연, 최진욱
2011A functional promoter polymorphism of the human IL18 gene is associated with aspirin-induced urticaria.김승현, 박해심
2001A Functional Study of Gap Junction in GJB2 Mutations Associated with Hereditary Hearing Loss박홍준, 이준호, 정연훈
2013A genetic effect of IL-5 receptor α polymorphism in patients with aspirin-exacerbated respiratory disease.김승현, 박해심, 신유섭, 예영민
2013A genome-wide association study identified new variants associated with the risk of chronic hepatitis B.정재연, 조성원
2013A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans.조남한
2017A Genome-Wide Association Study Identifies UTRN Gene Polymorphism for Restless Legs Syndrome in a Korean Population우현구, 최지혜

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