1.2 Cases of Infantile Spasms(Cryptogenic Type) Treated with ACTH Therapy.
Journal of the Korean Pediatric Society 1987;30(8):928-933
No abstract available.
Adrenocorticotropic Hormone*
2.Prevalence of hepatitis C virus antibody in Korean hemophiliacs.
Korean Journal of Hematology 1992;27(1):61-67
No abstract available.
Hepacivirus*
;
Hepatitis C*
;
Hepatitis*
;
Prevalence*
3.A Clinical Study and Comprehensive Total Care in Hemophilia.
Shin Heh KANG ; Chang Hyun YANG ; Kir Young KIM
Journal of the Korean Pediatric Society 1988;31(2):202-211
No abstract available.
Hemophilia A*
4.A Case of Renal Candidiasis Associated with Type I Diabetes Mellitus.
Shin Heh KANG ; Jae Seung LEE ; Duk Hi KIM
Journal of the Korean Pediatric Society 1987;30(6):677-683
No abstract available.
Candidiasis*
;
Diabetes Mellitus*
5.Factor VIII inhibitors in Korean hemophiliacs-I. prevalence of factor VIII inhibitors.
Shin Heh KANG ; Hae Ran MOON ; Kyung Soon SONG
Korean Journal of Hematology 1992;27(1):55-60
No abstract available.
Factor VIII*
;
Prevalence*
6.Sodium and calcium transport in spherocytic red blood cells.
Shin Heh KANG ; Kir Young KIM ; Young Ho LEE ; Bok Soon KANG
Journal of the Korean Pediatric Society 1991;34(7):978-991
No abstract available.
Calcium*
;
Erythrocytes*
;
Sodium*
;
Spherocytes
7.Ultrasonographic Diagnosis of Congenital Hypertrophic Pyloric Stenosis.
Shin Heh KANG ; Chul LEE ; Ran NAMGUNG ; Dong Gwan HAN ; Ki Keun OH ; Seung Hun CHOI
Journal of the Korean Pediatric Society 1989;32(6):756-764
No abstract available.
Diagnosis*
;
Pyloric Stenosis, Hypertrophic*
8.Clinical significance of RDW in childhood microcytic hypochromic anemia.
Moon Kyu KIM ; Shin Heh KANG ; Chang Hyun YANG ; Kir Young KIM
Korean Journal of Hematology 1991;26(1):51-57
No abstract available.
Anemia, Hypochromic*
9.A case of hemophilic pseudotumor in mandible.
Young Nae YIM ; Shin Heh KANG ; Chang Hyun YANG ; Kir Young KIM ; Tae Sub CHUNG
Korean Journal of Hematology 1991;26(1):213-217
No abstract available.
Mandible*
10.Subtypes of von Willebrand Disease Based on vWF Multimer Analysis in Korea.
Korean Journal of Pediatric Hematology-Oncology 2000;7(1):42-49
PURPOSE: von Willebrand disease is a common inherited bleeding disorder characterized by high degree of variable clinical presentation due to either quantitative or qualitative defects in von Willebrand factor. Its incidence in Korea is not well studied while that in western countries is extensively studied. METHODS: We classified 16 cases of vWD from 14 unrelated families based on vWF antigen, ristocetin cofactor activity, factor VIII activity and vWF multimeric patterns analysed by agarose gel electrophoresis, according to a revised classification by ISTH. RESULTS: There were 12 cases (75%) of type 1 vWD or 2M/2N with normal multimeric pattern, 3 cases (18.75%) of type 2 vWD lacking high molecular weight multimers and only 1 case of type 3 vWD with no multimers. CONCLUSION: The proportion of each vWD subtype in Korea is similar to that in western countries, however, accurate diagnosis based on ristocetin induced platelet aggregation test, factor VIII binding assay and molecular genetic diagnosis seems to be necessary for a more complete classification of vWD.
Classification
;
Diagnosis
;
Electrophoresis, Agar Gel
;
Factor VIII
;
Hemorrhage
;
Humans
;
Incidence
;
Korea*
;
Molecular Biology
;
Molecular Weight
;
Platelet Aggregation
;
Ristocetin
;
von Willebrand Disease, Type 3
;
von Willebrand Diseases*
;
von Willebrand Factor
Result Analysis
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