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Quality Assessment and Relevant Clinical Impact of Randomized Controlled Trials of Varicocele: Next Step to Good-Quality Randomized Controlled Trial of Varicocele Treatment

Kim KS, Chung JH, Park HJ, Shin WJ, Lee BH, Lee SW

Purpose: To assess the quality of randomized controlled trials (RCTs) on varicocele published from 1979 to 2017. Materials and Methods: We searched for original RCT on varicocele published between 1979 and...
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Direct Internal Fixation for Unstable Atlas Fractures

Shin JW, Suk KS, Kim HS, Yang JH, Kwon JW, Lee HM, Moon SH, Lee BH, Park SJ, Park Sr, Kim Sk

Purpose: To investigate the radiologic and clinical outcomes of direct internal fixation for unstable atlas fractures. Materials and Methods: This retrospective study included 12 patients with unstable atlas fractures surgically treated...
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Chest CT Imaging Features of the Pulmonary Sequelae in Four Patients with COVID-19

Kim TE, Kim SY, Lee BH

With the ongoing coronavirus disease 2019 (COVID-19) pandemic, there is an increasing interest in the sequelae and care in recovered patients. Although the long-term sequelae of COVID-19 are still unknown,...
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Jejunal Migration of the Stent-Graft Used for Common Hepatic Artery Pseudoaneurysm

Kim J, Lee BH

Hemorrhage after pancreaticobiliary surgery is an infrequent but fatal complication. It is primarily caused by rupture of the pseudoaneurysm, and treatment options include endovascular coil embolization or endovascular stent-graft placement....
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Persistent Trigeminal Artery Variant Terminating in the Ipsilateral Superior Cerebellar Artery

Park TY, Lee BH, Hwang YJ, Lee JY, Bae SH

Persistent trigeminal artery (PTA) represent an unusual remnant of the fetal carotid-basilar anastomosis. Persistent trigeminal artery variant (PTAV) is a rare anastomosis between the internal carotid artery and cerebellar artery,...
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Rapidly Progressive Parkinsonism and Dementia with No Insomnia due to the PRNP D178N Mutation

Park KW, Lee SH, Hwang YS, Kim KW, Park KY, Kim MJ, Lee Y, Choi Y, Lee BH, Chung SJ

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Hypoxia Regulates the Extracellular Matrix via Mitogen-Activated Protein Kinases Pathway in Cells Retrieved from the Human Intervertebral Disc

Kang YM, Shin EJ, Lee BH, Yang JH, Lee HM, Moon SH

Purpose: The present study aimed to identify the physiological characteristics of cells by investigating the change in gene expression and protein levels during extracellular matrix (ECM) synthesis in the intervertebral...
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Clinical Genetic Testing in Children with Kidney Disease

Kang E, Lee BH

Chronic kidney disease, the presence of structural and functional abnormalities in the kidneys, is associated with a lower quality of life and increased morbidity and mortality in children. Genetic etiologies...
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Geographical Isolation and Root-Associated Fungi in the Marine Terrains: A Step Toward Establishing a Strategy for Acquiring Unique Microbial Resources

Park JM, Hong JW, Lee W, Lee BH, You YH

This study aimed to understand whether the geo-ecological segregation of native plant species affects the root-associated fungal community. Rhizoplane (RP) and rhizosphere (RS) fungal microbiota of Sedum takesimense native to...
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Anomalous Origins of the Bilateral Vertebral Arteries Arising from the Aortic Arch: A Case Report

Park C, Lee BH

Various anomalous origins of the vertebral arteries (VAs) have been reported. However, anomalous origins of the bilateral VAs arising directly from the aortic arch are extremely rare. We encountered a...
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Efficacy of Living Donor Liver Transplantation in Patients with Methylmalonic Acidemia

Jang JG, Oh SH, Kim YB, Kim SH, Yoo HW, Lee BH, Namgoong JM, Kim DY, Kim KH, Song GW, Moon DB, Hwang S, Lee SG, Kim KM

Purpose: Despite aggressive medical and nutritional management, patients with methylmalonic acidemia (MMA) often suffer from multi-organ damage. Early deceased donor liver transplantation (DDLT) has emerged as an intervention to prevent...
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Neurofibromatosis type I: points to be considered by general pediatricians

Kang E, Yoon HM, Lee BH

Neurofibromatosis type 1 (NF1), a prevalent genetic disease that is transmitted in an autosomal dominant manner, is characterized by multiple cutaneous café-au-lait spots and neurofibromas as well as various degrees...
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A Novel Anti-PD-L1 Antibody Exhibits Antitumor Effects on Multiple Myeloma in Murine Models via Antibody-Dependent Cellular Cytotoxicity

Ahn JH, Lee BH, Kim SE, Kwon BE, Jeong H, Choi JR, Kim MJ, Park Y, Kim BS, Kim DH, Ko HJ

Multiple myeloma is a malignant cancer of plasma cells. Despite recent progress with immunomodulatory drugs and proteasome inhibitors, it remains an incurable disease that requires other strategies to overcome its...
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Nonepisodic angioedema with eosinophilia: A case report of a Korean patient

Choi J, Park SY, Moon KT, Lee WM, Lee BH, Kim SH

Nonepisodic angioedema with eosinophilia (NEAE) is a rare disease characterized by nonrecurrent angioedema with eosinophilia and normal serum IgM levels occurring predominantly in an East Asian female population. A 49-year-old...
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Effects of Chin-Down Maneuver on Pharyngeal Pressure Generation According to Dysphagia and Viscosity

Lee SM, Lee BH, Kim JW, Jang JY, Jang EG, Ryu JS

Objective To demonstrate the effects of chin-down maneuver on swallowing by using high-resolution manometry (HRM). Methods HRM data of 20 healthy subjects and 64 dysphagic patients were analyzed. Participants swallowed 5...
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Hypotonia, Ataxia, and Delayed Development Syndrome caused by the EBF3 mutation in a Korean boy with muscle hypotonia

Kim TG, Choi YH, Lee YN, Kang MJ, Seo GH, Lee BH

Hypotonia, Ataxia, and Delayed Development Syndrome (HADDS) is an autosomal-dominant, extremely rare neurodevelopmental disorder caused by the heterozygous EBF3 gene mutation. EBF3 is located on chromosome 10q26.3 and acts as...
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Refractory hyperkalemia caused by ACE gene mutation in a 3-yearold girl with kidney transplantation: a case report

Kim JY, Lee BH, Cho H

Background: Renal tubular dysgenesis (RTD) is rare and mostly fatal disease caused by genetic defect in renin-angiotensin system (RAS) presenting poor or absent development of proximal tubule. We report a...
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Campomelic Dysplasia with Sex Reversal Harboring a Novel Frameshift Mutation

Lee HN, Kim CY, Jung E, Lee BH, Lee BS, Kim EAR, Kim KS

Campomelic dysplasia (CD) is a rare genetic disease characterized by skeletal dysplasia that also affects several other organ systems. CD is caused by a SOX9 mutation. We here report a...
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Superior Mesenteric Venous Thrombophlebitis with Terminal Ileal Diverticulitis: A Case Report

Park Yi, Kim YH, Lee BH

Mesenteric venous thrombophlebitis secondary to inflammatory processes such as diverticulitis and appendicitis is a rare disease; however, it can nonetheless cause bowel ischemia and infarctions. Radiologic diagnosis is vital for...
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A Self-Efficacy Promotion Program for the Continuation of Breastfeeding for Mothers of Premature Infants

Lee Bh, Bang KS

Purpose: This study examined the effects of breastfeeding education among preterm mothers. Methods: A nonequivalent control group, repeated measure, quasi-experimental study design was used. The participants comprised 46 preterm mothers...
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