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Primary breast lymphoma

Sung DW, Lim JW, Yoon Y, Kim YW, Lee JH, Cho KS

We report the case of a 20-year-old female with lymphoma of the breast. Mammography showed an asymmetric pattern of confluent densities without any discrete mass. Sonography revealed diffuse heterogenous echoic...
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Metabolic alkalosis induced by plasmapheresis in a patient with systemic lupus erythematosus

Choi MY, Lee JD, Lee SH, Park IS, Woo JY, Choi EJ, Chang YS, Bang BK

We report a patient with systemic lupus erythematosus (SLE), who had developed metabolic alkalosis during plasmapheresis. The metabolic alkalosis could be promptly corrected by reducing the amount of citrate load....
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Central core disease

Myong NH, Suh YL, Chi JG, Hwang YS

Central core disease is a rare congenital myopathy characterized by the formation of cores that consist of abnormal arrangement of myofibrils inside the myofibers. We report a 5-year-old Korean girl...
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Peripheral neuropathy as a hypereosinophilic syndrome and anti-GM1 antibodies

Lee GH, Lee KW, Chi JG

The acute peripheral neuropathy as one of hypereosinophilic syndrome is known to be a rare disorder. The authors experienced a dramatic case with acute peripheral neuropathy, hypereosinophilia in peripheral blood,...
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Arterial thrombosis associated with nephrotic syndrome; a case report and review (adult cases in the English literature)

Kim HJ, Park CH, Kang CM, Park HC, Kim CY, Cho YS

The thromboembolic complications of nephrotic syndrome are reasonably common, including spontaneous peripheral venous and/or arterial, pulmonary arterial, and renal venous occlusions. However, in comparison to the relatively high incidence of...
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A case of juvenile form Pompe's disease manifested as chronic alveolar hypoventilation

Kim DG, Jung K, Lee MK, Hyun IG, Lim HJ, Song HG, Chi JG

We describe a case of the juvenile form of Pompe's disease that presented as primary alveolar hypoventilation due to respiratory muscle involvement. This 17-year-old girl had been asymptomatic until this...
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Fragile site X chromosomes in mentally retarded boys

Moon HR, Moon SY

The fragile X syndrome is a common X-linked mental retardation and autism, affecting females as well as males. The fragile site X chromosomes were studied in a series of 153...
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Urodynamic evaluation in pediatric neurogenic bladder

Kim KM, Choi H

Urodynamic evaluation in pediatric neurogenic bladder is prerequisite for accurate prediction of prognosis and selection of appropriate treatment modality. We classified normal, hyperreflexic and areflexic bladders by cystometry. Hyperreflexic bladder...
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Corporeal blood gas changes according to duration of drug-induced prolonged erection

Kim SC, Seo KK, Oh CH

The corporeal blood gas changes in accordance with the duration of the prolonged erection which developed after intracorporeal pharmacotherapy with papaverine and phentolamine were investigated in 62 impotence patients. The...
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Distribution of HLA class I alleles and haplotypes in Korean

Kim TG, Han H, Lim BU, Kim W, Kim SM

The antigen (phenotype), gene (allele) and haplotype frequencies of HLA class I were analysed in 4,622 Koreans. With allele frequencies of over 0.05, the most frequent HLA-A,-B and -C antigens...
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Leigh's disease involving multiple organs

Jung KC, Myong NH, Chi JG, Choi HR, Lee HS, Ahn YM

Leigh's disease is a rare progressive neurological disorder that is characterized light microscopically by focal spongy necrosis in the brain and electron microscopically by mitochondriopathy. We report an autopsy case...
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Early allograft function in canine single lung transplant

Sohn KH, Song MG, Lee JM, Song KS, Moon DH, Yu ES, Kim WD

An assessment of early graft function in canine single lung transplant recipients was made by analysing early postoperative radiographic progression, lung perfusion, bronchial patency and bronchial anastomotic wound healing and...
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Comparison of p53 gene mutations in paired primary and metastatic gastric tumor tissues

Kim JH, Choi JJ, Noh SH, Roh JK, Min JS, Youn JK, Yoo NC, Lim HY, Carbone DP, Gazdar AF, Lee KS, Kim BS

Our previous study revealed that mutations of the p53 gene were detected by cDNA sequencing in one of four (25%) primary gastric tumors and in five of six (83%) gastric...
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