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Showing results 1 to 20 of 513

Publication YearTitleAJOU
Author
2008A "benign" sphenoid ridge meningioma manifesting as a subarachnoid hemorrhage associated with tumor invasion into the middle cerebral artery.김호성김선용
2006A Case of Endoscopically Treated Jejunal Bleeding from Polyarteritis Nodosa권혁춘선주성원제환서창희이기명함기백김진홍
2017A Case of Giant Hydronephrosis Hidden by Obesity in an 11-year-old Boy추설호김현지배기수
2011A Case of Multiple Hepatocellular Carcinoma which was Performed Liver Transplantation after Down-staging by Transcatheter Arterial Chemoembolization왕희정김봉완조성원원제환
2009A Case of Osteomalacia with Multiple Fractures and Hypocalcemia Associated with Phenytoin Therapy정윤석곽규성홍지만원예연
2008A Case of Panhypopituitarism and Central Diabetes Insipidus Caused by Primary Central Nervous System Lymphoma안미선김순선김태호한승진김대중김효철김세혁한재호김호성정윤석
2009A Case of Primary Hyperparathyroidism with Pathologic Fracture, Osteitis Fibrosa Cystica and Hungry Bone Syndrome, Recovered after Parathyroidectomy김순선정윤석이두형김태호이기범곽규성
2014A case of secondary hypertension associated with the nutcracker phenomenon.원제환임홍석
2009A Case of Septo-optic Dysplasia Associated with Anterior Pituitary Hormone Abnormalities용석우안재홍김선용김호성정윤석
2010A Case Report of Hajdu-Cheney Syndrome안소연김옥화정윤석
2007A Case Report of Symptomatic Salivary Gland Rest within the Pituitary Gland김혜진김대중정윤석이관우김호성조경기
2012A Case with Spondyloepiphyseal Dysplasia Tarda with TRAPPC2 Mutation김옥화
2009A distinct form of spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL)-leptodactylic type: radiological characteristics in seven new patients.김옥화
2010A dominant mesomelic dysplasia associated with a 1.0-Mb microduplication of HOXD gene cluster at 2q31.1.김옥화
2006A double catheter technique for elongated middle cerebral artery bifurcation aneurysm.신용삼김호성김선용
2015A focal marked hypoechogenicity within an isoechoic thyroid nodule: is it a focal malignancy or not?하은주
2011A founder mutation of CANT1 common in Korean and Japanese Desbuquois dysplasia.김옥화
2016A Multicenter Prospective Validation Study for the Korean Thyroid Imaging Reporting and Data System in Patients with Thyroid Nodules하은주
2009A Novel COMP Gene Mutation in a Korean Kindred with Multiple Epiphyseal Dysplasia고정민곽규성김현주
2010A novel homozygous MMP2 mutation in a patient with Torg-Winchester syndrome.정선용김현주김옥화
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