1.Management of gout.
Young Hoon HONG ; Choong Ki LEE
Korean Journal of Medicine 2005;69(4):459-462
No abstract available.
Gout*
;
Hyperuricemia
2.Correction of Pixy Ear Deformity with Triangular Flap.
Journal of the Korean Society of Aesthetic Plastic Surgery 2001;7(1):75-77
No abstract available.
Congenital Abnormalities*
;
Ear*
3.A study on some biochemical tests in HBsAg(+) and/or anti-HCV(+) blood donors.
Young Kee KIM ; Young Chul OH ; Ki Hong KIM
Korean Journal of Blood Transfusion 1993;4(2):207-215
No abstract available.
Blood Donors*
;
Humans
4.A study on some biochemical tests in HBsAg(+) and/or anti-HCV(+) blood donors.
Young Kee KIM ; Young Chul OH ; Ki Hong KIM
Korean Journal of Blood Transfusion 1993;4(2):207-215
No abstract available.
Blood Donors*
;
Humans
5.Registration of Rho(D) negative blood donors.
Seon Ho LEE ; Young Chul OH ; Ki Hong KIM
Korean Journal of Blood Transfusion 1993;4(2):165-171
No abstract available.
Blood Donors*
;
Humans
6.Registration of Rho(D) negative blood donors.
Seon Ho LEE ; Young Chul OH ; Ki Hong KIM
Korean Journal of Blood Transfusion 1993;4(2):165-171
No abstract available.
Blood Donors*
;
Humans
7.Analysis of DNA ploidy patterns of anal condyloma acuminata: correlation with anal cancer.
Young Jin KIM ; Woon Ki HONG ; C Juan FELIX
Journal of the Korean Society of Coloproctology 1993;9(2):131-134
No abstract available.
Anus Neoplasms*
;
DNA*
;
Ploidies*
8.Analysis of DNA ploidy patterns of anal condyloma acuminata: correlation with anal cancer.
Young Jin KIM ; Woon Ki HONG ; C Juan FELIX
Journal of the Korean Society of Coloproctology 1993;9(2):131-134
No abstract available.
Anus Neoplasms*
;
DNA*
;
Ploidies*
9.Waveform analysis for the diplophonic voice.
Ki Hwan HONG ; Dong Suk CHUN ; Young Joong KIM
Korean Journal of Otolaryngology - Head and Neck Surgery 1993;36(5):1011-1017
No abstract available.
Voice*
10.Osteogenesis Imperfecta Tarda (Case Report Tow cases)
Chung Nam KANG ; Ki Hong CHOI ; Young Man PARK
The Journal of the Korean Orthopaedic Association 1976;11(3):309-315
Two cases report on osteogenesis imperfecta tarda and review of literature has been made. The rare genetic disorder, osteogenesis imperfecta tarda is familiar to most orthopedic surgeons because of management of fracture and skeletal deformities, espicially bowing of long bone. Its clinical manifestations are known as bony fragility, blue sclera and deafness less frequently ligamentous laxity but its etiological factor is obscure; The basic defect is thought to involvement some abnormality of collagen. Recently the bony weakness caused by increased bony turnover rate. One case of osteogenesis imberrfecta tarda in 8 year old male was belonged to tarda type 1. (Falvo-classification), who could not walk due to marked anterolateral bowing of right tibia and the another to tarda type II. in 13 year old male with fresh fracture of right femoral shaft. The former was performed corrective multible osteotomy, realignment and intramedullary rod fixation for correction of bowing deformity of right tibia, and the later was managed the fracture of right femoral shaft with Russels traction and hip spica cast. The result of reported therapeutic mesure was good.
Collagen
;
Congenital Abnormalities
;
Deafness
;
Fibrinogen
;
Hip
;
Humans
;
Ligaments
;
Male
;
Orthopedics
;
Osteogenesis Imperfecta
;
Osteogenesis
;
Osteotomy
;
Sclera
;
Surgeons
;
Tibia
;
Traction
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