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Factor VIII inhibitors in Korean hemophiliacs-I. prevalence of factor VIII inhibitors

Kang SH, Moon HR, Song KS

  • KMID: 1688211
  • Korean J Hematol.
  • 1992 May;27(1):55-60.
No abstract available.
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Supracondylar Fracture of the Humerus in a Hemophiliac with Antibodies to Factor VIII - A Case Report

Kho DH, Kim DH, Kim KH, Lim SW

  • KMID: 2331036
  • J Korean Fract Soc.
  • 2002 Jan;15(1):82-86.
Fractures in hemophiliacs with antibodies to factor VIII are very rare, and the presence of antibodies to factor VIII in the patient`s blood makes antihemophilic replacement therapy and operative treatment...
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Factor VIII Gene Inversions in Korean Patients with Severe Hemophilia A and its Application to Carrier Detection

Choi YM, Park SH, Jo SJ

  • KMID: 1568974
  • Korean J Obstet Gynecol.
  • 2000 Aug;43(8):1321-1325.
No abstract available.
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Recurrent Cerebral Venous Thrombosis Associated with Elevated Factor VIII

Kim MJ, Cho AH, No YJ, Kim HY, Kim JS

Cerebral venous thrombosis (CVT) rarely recurs, and the factors associated with a recurrence remain unclear. Recently, however, elevated plasma coagulation factor VIII has been considered a factor related to recurrent...
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A Case of Combined Congenital Deficiency of Factor V and Factor VIII

Cho KC, Lee SK, Kim IK, Sung H, Choi CH

  • KMID: 2335188
  • J Korean Pediatr Soc.
  • 1996 Aug;39(8):1162-1167.
Hemorrhagic disease of newborn by combined blood clotting factor deficiencies is very rare. Combined deficiency of factor V and factor VIII is the most common form among these cases, and...
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Anesthetic Management of Open Heart Surgery in a Patient with Hemophilia A: A case report

Kim KA, Bahk JH, Kim CS

We experienced a case of open heart surgery for correction of ventricular septal defect and patent ductus arteriosus in five years old boy with hemophilia A. Factor VIII activity in...
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An Autoplex Treatment in a Hemophilia A Patient with High Titer of Anticoagulant FVIII Antibody

Jeong JH, Choi YM

  • KMID: 2072465
  • Korean J Pediatr Hematol Oncol.
  • 1997 Apr;4(1):150-154.
Hemophilia A is a bleeding disorder resulting from a congenital deficiency of factor VIII. The mainstay of successful hemophilia therapy for either treatment or prevention of acute hemorrage is prompt...
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Cranial Hemophilic Pseudotumor: Case Report

Park JT, Kim GK, Lim YJ, Kim TS, Rhee BA, Leem W

  • KMID: 2018926
  • J Korean Neurosurg Soc.
  • 1996 Aug;25(8):1743-1748.
Hemophilic pseudotumor is an uncommon, but characteristic complication of hemophilia occurring in 1% to 2% of individuals with a severe factor VIII or IX deficiency. Most of these lesions are...
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A Case of Angiosarcoma of the Face and Scalp

Cho KH, Kang SJ, Lee YS, Kim CW

  • KMID: 2231534
  • Korean J Dermatol.
  • 1986 Dec;24(6):882-886.
We report a case of angiosarcoma of the face and scalp in a 76-year-old man. Immunochemical staining with factor 8-related antigen and ultrastructural find ings confirm that this tumor was...
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Plasminogen activator inhibitor(PAI-1) and factor VIII in acute lung injury

Kim HJ, Ahn CM, Lee KJ, Kim SK, Lee WY, Song KS

  • KMID: 1698024
  • Korean J Intern Med.
  • 1991 Dec;41(6):813-820.
No abstract available.
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Laparoscopic Cholecystectomy in a Hemophiliac Patient with Factor VIII Inhibitor

Choi HH, Chang HJ, Lee WJ, Kim BR

  • KMID: 2096302
  • J Korean Surg Soc.
  • 2005 Dec;69(6):488-492.
Hemophilia A is a severe bleeding disorder resulting from the lack of functional blood coagulation factor VIII. Accordingly, operations on patients with hemophilia A, except in a few cases, are...
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Factor VIII Related Antigen in Granuloma Pyogenicum

Hong DP, Kim JM, Lee ES

  • KMID: 2039039
  • Korean J Dermatol.
  • 1987 Feb;25(1):71-75.
Using Avidin-Biotin immunoperaxidase method, we investigate the distribution patterns of factor VIII related antigen in various areas of skin lesions of 14 granuloma pyogenicum. and in the skin lesions of...
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Restriction fragment length polymorphisms of Dx13/BgI II associated with factor VIII: C gene in Koreans

Chung SR, Lee NB, Moon H, Lee CG, Lyu MS, Kim CR, Lee H, Kim YS, Koh JK

  • KMID: 2259421
  • Korean J Obstet Gynecol.
  • 1992 Jul;35(7):1038-1044.
No abstract available.
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Unexpected Bleeding Following Endoscopic Sinus Surgery Leading to the Rare Diagnosis of Acquired Haemophilia A

Ahn SH, Kim YW, Im DH, Kim JK

We report a case of acquired hemophilia A following endoscopic sinus surgery. The patient was a 64-year-old man whose preoperative activated partial thromboplastin time (aPTT) was slightly prolonged. He underwent...
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A Case of Cerebral Venous Thrombosis Associated with Increased Factor VIII in Hyperthyroidism

Sinn DI, Kwon SJ, Hong YH, Lee KW

  • KMID: 2065609
  • J Korean Neurol Assoc.
  • 2006 Oct;24(5):472-474.
Cerebral venous thrombosis (CVT) is a multifactorial disease characterized by various clinical manifestations and predisposing factors. The association of CVT with hyperthyroidism has been suggested and the high plasma level...
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Two patients with acquired hemophilia successfully treated with combination therapy including therapeutic plasmapheresis

Park E, Jang JS, Park S, Lee SJ

  • KMID: 2258445
  • Korean J Med.
  • 2009 Sep;77(3):367-370.
Acquired hemophilia is a rare disorder associated with fatal bleeding caused by the development of autoantibodies against factor VIII. Here, we report the cases of two young women with acquired...
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A case of acquired hemophilia detected after influenza vaccination

Chung BH, Kim YJ, Kim MS, Kim JY, Shin DI, Kim YS, Bang BK

  • KMID: 1867070
  • Korean J Med.
  • 2004 Mar;66(3):298-301.
Acquired hemophilia is a rare disorder associated with development of factor VIII inhibitors. Acquired inhibitors against factor VIII in nonhemophilic patients are associated with various conditions, including autoimmune diseases, malignancies,...
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Acquired Hemophilia: Successfully Treated with Plasma Exchange in a Patient with Hightiter Inhibitors

Kim YK, Suh JS

  • KMID: 1440723
  • Korean J Blood Transfus.
  • 2012 Apr;23(1):68-71.
Acquired hemophilia is an extremely rare but life threatening hemorrhagic disease caused by autoantibodies directed coagulation factor VIII. Estimated management guidelines include rapid diagnosis, suppression of bleeding, and elimination of...
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Genetic Risk Factors of Hemophilia A

Shim YJ, Lee KS

  • KMID: 2135606
  • J Genet Med.
  • 2010 Jun;7(1):1-8.
Hemophilia A is a sex-linked recessive coagulation disorder associated with diverse mutations of the factor VIII gene and a variety of phenotypes. The type of mutation involved dictates the activity...
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Acquired factor VIII deficiency after consuming the dried gallbladder of a cobra, Naja naja

Kim HJ, Lee WS, Lee YJ, Jun HS, Seo SK, Joo YD

Acquired factor VIII deficiency is very rare, often fatal. It is associated with pregnancy, autoimmune diseases, malignancy, and drugs, although no underlying cause is found in 50%. A 49-year-old male...
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