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Advancements in the treatment of pediatric acute leukemia and brain tumor - continuous efforts for 100% cure

Ju HY, Hong CR, Shin HY

Treatment outcomes of pediatric cancers have improved greatly with the development of improved treatment protocols, new drugs, and better supportive measures, resulting in overall survival rates greater than 70%. Survival...
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Inhaled iloprost for the treatment of patient with Fontan circulation

Kim YH, Chae MH, Choi DY

Decreased exercise capacity after Fontan surgery is relatively common and the failure of the Fontan state gradually increases with age. However, there is no further treatment for patients with Fontan...
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Adrenal and thyroid function in the fetus and preterm infant

Chung HR

Adrenal and thyroid hormones are essential for the regulation of intrauterine homeostasis, and for the timely differentiation and maturation of fetal organs. These hormones play complex roles during fetal life,...
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Overlapping Guillain-Barre syndrome and Bickerstaff's brainstem encephalitis associated with Epstein Barr virus

Rho YI

A flaccid tetraparesis in Bickerstaff's brainstem encephalitis (BBE) is presumed to be a sign of overlapping Guillain-Barre syndrome (GBS). In addition, BBE and Fisher syndrome, which are clinically similar and...
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Serum interleukin-1beta and tumor necrosis factor-alpha in febrile seizures: is there a link?

Mahyar A, Ayazi P, Orangpour , Daneshi-Kohan MM, Sarokhani , Javadi A, Habibi M, Talebi-Bakhshayesh M

PURPOSE: Febrile seizures are induced by fever and are the most common type of seizures in children. Although numerous studies have been performed on febrile seizures, their pathophysiology remains unclear....
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Serum procalcitonin as a diagnostic marker of neonatal sepsis

Park IH, Lee SH, Yu ST, Oh YK

PURPOSE: We evaluated serum procalcitonin (PCT) as a diagnostic marker of neonatal sepsis, and compared PCT levels with C-reactive protein (CRP) levels. METHODS: We retrospectively reviewed the medical records of 269...
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The large-conductance calcium-activated potassium channel holds the key to the conundrum of familial hypokalemic periodic paralysis

Kim JB, Kim SJ, Kang SY, Yi JW, Kim SM

PURPOSE: Familial hypokalemic periodic paralysis (HOKPP) is an autosomal dominant channelopathy characterized by episodic attacks of muscle weakness and hypokalemia. Mutations in the calcium channel gene, CACNA1S, or the sodium...
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