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An Endobronchial Lipoma Treated by Bronchoscopic Excision

Choi SH, Kang JY, Joo YB, Kim SK, Mo EY, Lee SH, Moon HS

  • KMID: 2259003
  • Korean J Med.
  • 2011 Mar;80(3):337-342.
A 68-year-old man presented with partial atelectasis of the right middle lobe on chest X-ray. Computed tomography of the chest revealed a hypodense mass in the middle lobe. Bronchoscopy showed...
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A Case of Multidrug-resistant Acinetobacter baumannii Ventriculitis Successfully Treated with Intrathecal Colistimethate

Hong YA, Yoo JH, Kim JJ, Mo EY, Ahn GH, Jeong HK, Kim JS, Lee HJ, Jung MH, Yoon SB

Acinetobacter species is a non-fermentative aerobic gram-negative coccobacillus that is an important pathogen found in nosocomial infections. Recently, multi-drug resistant Acinetobacter baumannii (MDR-AB) infections have been increasing and pose a...
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A Case of Acute Pyelonephritis Complicated with Renal Vein Thrombosis

Lee HJ, Jung MH, Jeong HK, Kim JJ, Mo EY, Kim YK, Song HC, Choi EJ

  • KMID: 2253209
  • Korean J Nephrol.
  • 2009 Jan;28(1):63-66.
Acute pyelonephritis is a common disease in clinical practice. Renal vein thrombosis in acute pyelonephritis has become a rare complication at present because of the advances of antibiotics. The trend...
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The usefulness of endoscopic hemostasis with hemoclipping in acute colonic diverticular bleeding

Mo EY, Jung ME, Kim JJ, Kim SJ, Do KR, Kim HK, Kim SS, Chae HS, Cho YS

  • KMID: 2259116
  • Korean J Med.
  • 2010 Aug;79(2):148-154.
BACKGROUND/AIMS: Although colonoscopy is often used to diagnose and treat acute lower gastrointestinal bleeding, there have been few reports on outcomes of the management of colonic diverticular bleeding in Korea....
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Clinical features and signaling effects of RET D631Y variant multiple endocrine neoplasia type 2 (MEN2)

Lee Jy, Kim SY, Jo KH, Mo EY, Kim ES, Kim HS, Han JH, Moon Sd

Background/Aims: Germline mutations of the rearranged during transfection (RET) gene cause multiple endocrine neoplasia type 2 (MEN2). About 85% of RET mutations in MEN2 occur in codon Cys634. The RET...
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Functional Identification of Compound Heterozygous Mutations in the CYP17A1 Gene Resulting in Combined 17α-Hydroxylase/17,20-Lyase Deficiency

Mo EY, Lee JY, Kim SY, Kim MJ, Kim ES, Lee S, Han JH, Moon SD

BACKGROUND: We previously reported a patient with congenital adrenal hyperplasia (CAH) with compound heterozygous mutations in the cytochrome P450 17A1 (CYP17A1) gene. One allele had a p.His373Leu and the other...
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