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Showing results 241 to 257 of 257

Pub YearTitleAuthor(s)
2015The Total Calvarial Remodeling with Transsutural Distraction Osteogenesis of 21 Cases of Craniosynostosis: New, Efficient, Safe and Natural Method in Craniosynostosis Surgery.박동하, 윤수한
2017The Total Calvarial Transsutural Distraction Osteogenesis for 26 Children with Slit Ventricle, Craniosynostosis, or Microcephaly After Shunt Operation박동하, 윤수한
2012The Visible Human Projects in Korea and China with improved images and diverse applications신동선, 정민석
2018Torticollis Caused by Nontraumatic Craniovertebral Junction Abnormalities김상현, 박성훈, 임신영
2023Twenty-Five Year Trend Change in the Etiology of Pediatric Invasive Bacterial Infections in Korea, 1996-2020정현주
2013Two cases of Kawasaki disease with hidden neuroblastoma.박준은, 정현주
2017Two histopathological patterns of postinflammatory hyperpigmentation: epidermal and dermal강희영, 권지은, 김유찬, 이은소
2012Two novel insulin receptor gene mutations in a patient with Rabson-Mendenhall syndrome: the first Korean case confirmed by biochemical, and molecular evidence손영배
2000US in the diagnosis of pediatric chest diseases.김옥화, 서정호
2015Use of Medical Resources by Preterm Infants Born at Less than 33 Weeks' Gestation Following Discharge from the Neonatal Intensive Care Unit in Korea.이장훈
2012Usefulness of dynamic contrast-enhanced MRI in differentiating between septic arthritis and transient synovitis in the hip joint곽규성, 윤승현, 이두형, 조재호
2017Usefulness of end-tidal carbon dioxide as an indicator of dehydration in pediatric emergency departments: A retrospective observational study민영기, 이지숙
1995Variability of in vivo recovery of factor IX after infusion of monoclonal antibody purified factor IX concentrates in patients with hemophilia B. The Mononine Study Group.김효철
1999Very long chain acyl coenzyme A dehydrogenase deficiency in a 5-month-old Korean boy: identification of a novel mutation.정조원, 한시훈, 홍창호
2011Vitamin D: A View of Perinatal Medicine이장훈
2019Which growth parameters can affect mortality in cerebral palsy?임신영
2011Whole-exome sequencing detects somatic mutations of IDH1 in metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria (MC-HGA).김옥화
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