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Showing results 41 to 60 of 2113

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Issue DateTitleJournal Title
2011A Case of Mediastinal and Pulmonary Cryptococcosis in a 3-Year-Old Immunocompetent Girl Pediatric Allergy and Respiratory Disease (소아알레르기 호흡기학회지)
2011A Case of Metachromatic Leukodystrophy Confirmed by Molecular Genetic Analysis Journal of the Korean Child Neurology Society
2006A Case of Multiple Endocrine Neoplasia Type 2B early Diagnosis by RET Proto-oncogene Analysis and Proplactic TotalThyroidetomy Journal of Korean Society of Pediatric Endocrinology (대한소아내분비학회지)
2005A case of multiple giant coronary aneurysms with large mural thrombus due to Kawasaki disease in a young infant Korean Journal of Pediatrics
2010A case of Ohtahara syndrome with mitochondrial respiratory chain complex I deficiencyBRAIN & DEVELOPMENT
2010A case of postoperative nasopharyngeal reflux associated with retropharyngeal lymphangioma in newborn infant Korean Journal of Pediatrics
2020A case of primary hyperparathyroidism due to an intrathymic ectopic parathyroid adenoma in a 15-year-old boy ANNALS OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
2016A Case of Pulmonary Interstitial Emphysema Treated by Percutaneous Catheter Insertion in Extremely Low Birth Weight Infant YONSEI MEDICAL JOURNAL
2010A case of Rubinstein-Taybi Syndrome with a CREB-binding protein gene mutation Korean Journal of Pediatrics
2009A case of suspected isotretinoin-induced malformation in a baby of a mother who became pregnant one month after discontinuation of the drug. YONSEI MEDICAL JOURNAL
2014A case of thyrotoxic periodic paralysis as initial manifestation of Graves' disease in a 16-year-old Korean adolescent ANNALS OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
2019A Child With Lymphangioma Due to Somatic Mutation in PIK3CA Successfully Treated With EverolimusPEDIATRIC NEUROLOGY
2020A Comprehensive Analysis of Clinical Trials in the COVID-19 Pandemic Era MEDICINA-LITHUANIA
2019A deep learning model for real-time mortality prediction in critically ill children CRITICAL CARE
2007A der(1;15)(q10;q10) is a rare nonrandom whole-arm translocation in patients with acute lymphoblastic leukemiaCANCER GENETICS AND CYTOGENETICS
2014A female carrier of ornithine carbamoyltransferase deficiency masquerading as attention deficit-hyperactivity disorderBRAIN & DEVELOPMENT
2007A five-year-old boy with nephrotic syndrome complicated with acute acalculous cholecystitisPEDIATRICS INTERNATIONAL
2012A foreign body found incidentally in a pediatric patient who was unable to communicate a foreign body found incidentally in a pediatric patient who was unable to communicateJOURNAL OF EMERGENCY MEDICINE
2007A Good Outcome for a Case of Chronic Pneumonitis of Infancy YONSEI MEDICAL JOURNAL
2003A haplotype-based molecular analysis of CFTR mutations associated with respiratory and pancreatic diseases HUMAN MOLECULAR GENETICS

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