1.Blood Component Therapy.
Journal of the Korean Pediatric Society 1986;29(12):1-5
No abstract available.
2.Statistical analysis of hemolytic anemia in Korea.
Korean Journal of Hematology 1991;26(2):445-461
No abstract available.
Anemia, Hemolytic*
;
Korea*
3.A Study on Clinical Course Prognosis and Therapeutic Effect in Childhood ITP.
Journal of the Korean Pediatric Society 1987;30(8):874-881
No abstract available.
Prognosis*
4.Role of aldosterone on the minimal change nephrotic syndrome in children.
Soon Wha KIM ; Myung Ik LEE ; Don Hee AHN
Journal of the Korean Pediatric Society 1989;32(11):1526-1532
No abstract available.
Aldosterone*
;
Child*
;
Humans
;
Nephrosis, Lipoid*
5.A Case of Stage IV-S Neuroblastoma with N-myc Amplification and Coagulopathy.
Min Ji KIM ; Yoon Ah SUNG ; Don Hee AHN
Korean Journal of Pediatric Hematology-Oncology 1997;4(1):161-166
Neuroblastoma stage IV-S patients have frequent spontaneous remission and high survival rate. Many investigators have recommended minimal or no therapeutic intervention ; however, some patient do experience progressive disease and ultimately die of neuroblastoma. We experienced a case of stage IVS neuroblastoma with N-myc amplification and coagulopathy. This patient has treated with combination chemotherapy and radiation therapy, then remained disease free for 1 year on the follow up till March, 1997.
Drug Therapy, Combination
;
Follow-Up Studies
;
Humans
;
Neuroblastoma*
;
Remission, Spontaneous
;
Research Personnel
;
Survival Rate
6.Clinical observation on Reye syndrome according to the onset of age in children.
Kyung Hee KIM ; Baik Hee LEE ; Myung Ik LEE ; Don Hee AHN ; Keun Chan SOHN
Journal of the Korean Pediatric Society 1992;35(6):788-794
No abstract available.
Child*
;
Humans
;
Reye Syndrome*
7.A case of hypodipsic hypernatremia.
Seung Hee PARK ; Hong Sin JEON ; Sun Hwa KIM ; Don Hee AHN
Journal of the Korean Pediatric Society 1993;36(11):1621-1625
Hypodipsic hypernatremia is characterized by chronic or recurrent episodes of severe hypernatermia associated with dehydration and a lack of thirst. This constellation of deficits suggests that the syndrome is due to hypodipsia of destruction of the hypothalamic osmoreceptors that regulate thirst and ADH secretion. We report a child with abnormalities of the central nervous system who had hypernatremia and a lack of thirst without detectable abnormalities in the osmoregulation of ADH secretion. The patient was a 11 month old female and her chief complaints were poor oral intake and weight gain. There were recurrent hypernatremia with hyperosmosis and normal level of plasma ADH. With intravenous rehydratin, oral intake was improved and plasma sodium level decreased.
Central Nervous System
;
Child
;
Dehydration
;
Female
;
Humans
;
Hypernatremia*
;
Infant
;
Osmoregulation
;
Plasma
;
Sodium
;
Thirst
;
Weight Gain
8.A Case of Symmetrical Peripheral Gangrene in Disseminated Intravascular Coagulation.
Mi Jeong KIM ; Seung Hee PARK ; Sun Wha KIM ; Don Hee AHN
Journal of the Korean Pediatric Society 1994;37(11):1620-1623
The symmetrical peripheral gangrene syndrome consists of sudden onset of symmetrical gangrene of the fingers, toes and more raely, the nose, upper lip, ear lobes, or genitalia. There is no evidence of occulusion of large vessels or vasculitis. We experienced a case of symmetrical peripheral gangrene developed in fingers and toes with disseminated intravascular coagulation in 20 day-old permature infant with sepsis by Enterobacter aerogenes. Thereafter, we presented a case with a brief review of the related literatures.
Disseminated Intravascular Coagulation*
;
Ear
;
Enterobacter aerogenes
;
Fingers
;
Gangrene*
;
Genitalia
;
Humans
;
Infant
;
Lip
;
Nose
;
Sepsis
;
Toes
;
Vasculitis
9.Follow up study of urinary tract infection associated with vesicoureteral reflux.
Kyung Hee KIM ; Young Jin HONG ; Soon Wha KIM ; Don Hee AHN
Journal of the Korean Pediatric Society 1992;35(12):1713-1721
No abstract available.
Follow-Up Studies*
;
Urinary Tract Infections*
;
Urinary Tract*
;
Vesico-Ureteral Reflux*
10.A Case of Bart's Syndrome.
Hong Shin JEON ; Young Jin HONG ; Don Hee AHN ; Hee Jun YOO ; Je Geun CHI
Journal of the Korean Pediatric Society 1994;37(1):104-108
A female newborn had the following characteristics; a congenital localized absence of skin over the lower extremities; blistering of the skin or mucous membrane, incited by trauma, which heals without scarring; and congenital absence or deformity of the nails. In respect to the characteristic manifestation, clinical course and electron microscopic features, our patient seems to fit well into Bart's syndrome. The inheritance pattern appears to be autosomal dominant but, as in this report, isolated cases have been recognized. As the review of the literatures, congenital localized absence of skin has been observed in various subsets of inherited E.B. But, we believe that the term Bart's syndrome should be used to identify patients with good prognosis as the Bart's initial description To the best of our knowedge, this is the first reported case of Bart's syndrome in the korean literature.
Blister
;
Cicatrix
;
Congenital Abnormalities
;
Female
;
Humans
;
Infant, Newborn
;
Inheritance Patterns
;
Lower Extremity
;
Mucous Membrane
;
Prognosis
;
Skin