Browsing "Radiology" by Keyword : Child

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Showing results 21 to 55 of 55

Pub YearTitleAuthor(s)
2021Establishment of Local Diagnostic Reference Levels of Pediatric Abdominopelvic and Chest CT Examinations Based on the Body Weight and Size in Korea박지은
2015Ethanol ablation of predominantly cystic thyroid nodules: evaluation of recurrence rate and factors related to recurrence.하은주
2021Evaluation of frequency-selective non-linear blending technique on brain CT in postoperative children with Moyamoya disease박지은
2018Feasibility of improved motion-sensitized driven-equilibrium (iMSDE) prepared 3D T1-weighted imaging in the diagnosis of vertebrobasilar artery dissection김선용, 이진수, 최진욱, 한미란, 홍지만
2017Head CT: Image quality improvement with ASIR-V using a reduced radiation dose protocol for children김현지
2013Identification of a GDF5 mutation in a Korean patient with brachydactyly type C without foot involvement.김옥화
2011Identification of signal peptide domain SOST mutations in autosomal dominant craniodiaphyseal dysplasia.김옥화
2007Imaging features of gastrointestinal tract duplications in infants and children: from oesophagus to rectum.김옥화
1995Imaging of the choledochal cyst.김옥화
2018Initial experience with synthetic MRI of the knee at 3T: comparison with conventional T1 weighted imaging and T2 mapping곽규성, 박성훈
2013Integrative analysis of congenital muscular torticollis: from gene expression to clinical significance.곽규성, 김장희, 박래웅, 박명철, 소의영, 이기영, 이명애, 이일재, 이정훈, 임신영
2022Lymphatic-Venous Malformation Presenting as a Mediastinal Mass in a 6-Year-Old Boy김석휘, 김중헌, 박지은, 장전엽
2012Metaphyseal chondromatosis combined with D-2-hydroxyglutaric aciduria in four patients김옥화
2013Osteogenesis imperfecta type V: clinical and radiographic manifestations in mutation confirmed patients.김옥화
2012PAPSS2 mutations cause autosomal recessive brachyolmia김옥화
2004Percutaneous sclerotherapy of lymphangiomas with acetic acid.김철호, 원제환
2017Plugged percutaneous biopsy of the liver in living-donor liver transplantation recipients suspected to have graft rejection김봉완, 김영배, 김진우, 왕희정, 원제환
2021Posterior lung herniation in pulmonary agenesis and aplasia: Chest radiograph and cross-sectional imaging correlation박지은
2020Prospective Multicenter Study of the Safety of Gadoteridol in 6163 Patients한미란
2011Pulmonary manifestations in Proteus syndrome: pulmonary varicosities and bullous lung disease.김옥화
2019Pupil-Involving Oculomotor Nerve Palsy Following Tonsillectomy and Adenoidectomy정승아, 한미란
2017Quantification of myelin in children using multiparametric quantitative MRI: a pilot study김현지, 최진욱
2017Reappraisal of Pediatric Diastatic Skull Fractures in the 3-Dimensional CT Era: Clinical Characteristics and Comparison of Diagnostic Accuracy of Simple Skull X-Ray, 2-Dimensional CT, and 3-Dimensional CT김현지, 윤수한
2011Revisit of multiple epiphyseal dysplasia: ethnic difference in genotypes and comparison of radiographic features linked to the COMP and MATN3 genes.김옥화
2007Septic arthritis versus transient synovitis of the hip: gadolinium-enhanced MRI finding of decreased perfusion at the femoral epiphysis.곽규성, 김선용, 이제희, 조재호
2017Septic pulmonary embolism resulting from soft tissue infection in a 5-year-old child김현지, 이수영, 이한동, 정경욱, 조재호
2010Spondylo-epiphyseal dysplasia, Maroteaux type (pseudo-Morquio syndrome type 2), and parastremmatic dysplasia are caused by TRPV4 mutations.김옥화
2021The relationship between ultrasound findings and thyroid function in children and adolescent autoimmune diffuse thyroid diseases박지은
2018Torticollis Caused by Nontraumatic Craniovertebral Junction Abnormalities김상현, 박성훈, 임신영
2012TRPV4-pathy manifesting both skeletal dysplasia and peripheral neuropathy: a report of three patients김옥화
2000US in the diagnosis of pediatric chest diseases.김옥화, 서정호
2012Usefulness of dynamic contrast-enhanced MRI in differentiating between septic arthritis and transient synovitis in the hip joint곽규성, 윤승현, 이두형, 조재호
2015Web-Based Malignancy Risk Estimation for Thyroid Nodules Using Ultrasonography Characteristics: Development and Validation of a Predictive Model.하은주
2011Whole-exome sequencing identifies mutations of KIF22 in spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type.김옥화
1998Wyburn-Mason syndrome: an unusual presentation of bilateral orbital and unilateral brain arteriovenous malformations.김옥화, 서정호, 유호민
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