- Original Article
- Plasma G-CSF and GM-CSF Concentration and Amount of Their
Receptors on the Granulocyte in Kawasaki Disease
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Young-Kyoung Yoo, Gibum Lee, Hyun-Hee Kim, Soo-Young Kim, You-Jeong Kim, Wonbae Lee
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Clin Exp Pediatr. 2003;46(4):376-381. Published online April 15, 2003
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Purpose : This study aimed to demonstrate the possible pathogenesis of granulopoiesis in patients of Kawasaki disease(KD) using quantitative analysis of G-CSF, GM-CSF and their CSFr.
Methods : The plasma levels of G-CSF, GM-CSF, G-CSFr and GM-CSFr were studied in 14 patients in the acute phase of KD; 13 children with normal peripheral white blood cell counts were used as the... |
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- Case Report
- Fanconi-Bickel Syndrome Presented with Diabetes
Mellitus and Galactosemia : Identification of a
Novel Mutation in the GLUT2 Gene
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You-Jeong Kim, Sun-Hee Rim, Young-Lim Shin, Han-Wook Yoo
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Clin Exp Pediatr. 2001;44(10):1201-1205. Published online October 15, 2001
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Fanconi-Bickel syndrome is a rare autosomal recessive disorder of the carbohydrate metabolism recently demonstrated to be caused by mutations in GLUT2, the gene for the glucose transporter protein 2 expressed in the liver, pancreatic β islet-cells, intestine and kidney. Typical clinical and laboratory findings of Fanconi-Bickel syndrome are hepatomegaly secondary to glycogen accumulation, glucose and galactose intolerance, fasting hypoglycemia, a... |
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