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Retrograde Transcatheter Closure of a Large Coronary Artery Fistula using an Amplatzer Vascular Plug

Cho YK, Yeo CY, Chung HY, Kim JH, Ma JS

  • KMID: 1514184
  • Chonnam Med J.
  • 2006 Dec;42(3):207-210.
Coronary artery fistulas (CAF) are rare anomalies in which blood is shunted into a cardiac chamber, great vessel or other structure. We report a successful retrograde transcatheter closure of congenital...
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A Clinical Study of Hereditary Spherocytosis

Kim DG, Yeo CY, Han DG, Baik HJ, Kook H, Hwang TJ

  • KMID: 1514177
  • Chonnam Med J.
  • 2006 Dec;42(3):174-179.
ion of 0.65% NaCl solution and completed at 0.38%. Splenectomy was performed in 13 with concomitant cholecystectomy in 6 out of 13, indication of which was frequent transfusions due to...
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A Clinical Study on the Patients with Viral Croup

Yeo CY, Lee SU, Cho YK, Jung HY, Ma JS

  • KMID: 1514179
  • Chonnam Med J.
  • 2006 Dec;42(3):187-191.
Viral croup is the most common cause of upper airway obstruction in children 6 months to 6 years of age. In this study, we analyzed the clinical course, evaluation and...
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Occlusion of the Patent Ductus Arteriosus with Cook Detachable Coil

Lee SU, Yeo CY, Cho YK, Choi IS, Chung HY, Ma JS

  • KMID: 2274907
  • Chonnam Med J.
  • 2007 Aug;43(2):123-128.
Percutanous closure with occluding coils has been recentely described as a method of nonsurgical treatment of the small patent ductus arteriosus (PDA). Several different devices were evaluated for the percutaneous...
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Clinical disease characteristics according to karyotype in Turner syndrome

Yeo CY, Kim CJ, Woo YJ, Lee DY, Kim MS, Kim EY, Kim JD

PURPOSE: Turner syndrome (TS) is a disorder in which various anomalies can be accompanied, especially cardiovascular, renal, thyroid and auditory problems. The aim of this study is to identify the...
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An Arg1239His mutation of the CACNL1A3 gene in a Korean family with hypokalemic periodic paralysis

Yeo CY, Kim YO, Kim MK, Kim JY, Cho YK, Kim CJ, Woo YJ

Familial hypokalemic periodic paralysis (hypoPP) is a rare inherited channelopathy that often presents with episodic weakness accompanied by hypokalemia. Thus far, mutations in the gene encoding two ion channels (CACNL1A3,...
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A case of megalencephalic leukoencephalopathy with subcortical cysts

Park EY, Kim YO, Kim JY, Yeo CY, Baek HJ, Kim CJ, Kim EY, Woo YJ

Megalencephalic leukoencephalopathy with subcortical cysts (MLC) is a rare white matter disorder, first described in the early 1990s. The brain in patients with MLC appears swollen on MRI, with diffuse...
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Causes of Precocious Puberty : Multicenter Study in Honam Area

Na JM, Lee YJ, Kim MS, Lee DY, Yeo CY, Kim CJ, Kim JD, Kim EY

  • KMID: 1819677
  • J Korean Soc Pediatr Endocrinol.
  • 2009 Jun;14(1):30-37.
PURPOSE:We analysed the spectrum of diagnoses made in a consecutive group of children referred for signs of precocious puberty and evaluated the clinical and endocrinologic characteristics. METHODS:Retrospective analysis of 375 children...
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Predicting Factors for Neurologic Outcome in Full-term Neonates with Hypoxic-Ischemic Encephalopathy

Yeo CY, Kim DK, Kim SH, Song ES, Woo YJ, Choi YY

  • KMID: 2099108
  • J Korean Soc Neonatol.
  • 2006 Nov;13(2):226-232.
PURPOSE:Hypoxic injury during delivery and subsequent ischemic encephalopathy is still remained as one of the important cause of neonatal death and associated with neurologic complication. We investigated the predicting factors...
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