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Clinical characteristics in hemophilia patients

Lee KS, Kim ES, Seo JS

  • KMID: 1690805
  • J Korean Pediatr Soc.
  • 1992 Nov;35(11):1501-1508.
No abstract available.
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Iliacus Hematoma with Femoral Neuropathy in Hemophilia: A Case report

Choi HY, Lee JH, Choi ST, Kim NS, Kim CJ, Yu HC

Hemophilia, a genetically determined disorder, can be divided into hemophilia A and hemophilia B. Hemophilia A, defined as a sex-linked recessive trait hemorrhagic disease of males characterized by a deficiency...
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Management of hemophilia in Korea: the past, present, and future

Choi EJ

No abstract available.
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A Case of Desensitization for Hemophilia B Inhibitor Patient with Anaphylaxis to FIX Concentrates

Park Y, Yoo KY

Among the patients with hemophilia, 10~15% have hemophilia B, and 1~3% of the hemophilia B patients develop inhibitor to factor IX clotting activity. Allergic reactions to concentrates containing factor IX...
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A Case of Hemophilia B Diagnosed after Rhinosinus Surgery in 37 Year-Old Patient

Kim HD, Choi IS

Hemophilia is an X-linked recessive disorder, which is classified into hemophilia A, defined by factor VIII deficiency and hemophilia B, defined by factor IX deficiency. The usual clinical presentation is...
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Clinical Studies on 100 Cases of Hemophilia

Shin MJ, Ko KW

  • KMID: 1698850
  • J Korean Pediatr Soc.
  • 1984 Sep;27(9):883-895.
No abstract available.
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Hemophilia

Yoo KY

Hemophilia is the most common coagulation disorder. It has a long history. Hemophilia A is caused by FVIII gene mutation, and hemophilia B by FIX gene mutation. Those genes are...
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A case of prenatal diagnosis of hemophilia A

Song KS, Lee A, Lee K, Lee BS

Classic hemophilia, (hemophilia A), is an X-linked hereditary bleeding disorder affecting half of the male offspring of female carriers. Prenatal diagnosis offers an option, namely to restrict abortions to...
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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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A Clinical Study and Comprehensive Total Care in Hemophilia

Kang SH, Yang CH, Kim KY

  • KMID: 1682540
  • J Korean Pediatr Soc.
  • 1988 Feb;31(2):202-211.
No abstract available.
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Successful Non-operative Management of Intra-abdominal Hemorrhage in Two Patients with Hemophilia A

Kim MJ, Lee EH, Yoon HS

Spontaneous intra-abdominal hemorrhages are uncommon in hemophilic patients. They can cause complications in patients with severe hemophilia, and are associated with a high mortality rate. To date, there is no...
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Attempts to treat patients with hemophilia, the "royal disease"

Park R

No abstract available.
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Treatment of Bleeding in Hemophilia

Yoon HJ

The management of hemophilia patients includes the treatment of acute bleeding, prevention of bleeding, and the treatment of complications. Bleeding can be minimized by prophylactic factor maintenance, education, and lifestyle...
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Shock Wave Lithotripsy in a Hemophilia Patient

Park CH, An JT, Cho CH, Woo IS, Park HW, Kim KK

  • KMID: 2060775
  • Korean J Urol.
  • 1999 Feb;40(2):240-241.
Shock wave lithotripsy(SWL) has been considered as a contraindication in a patient with bleeding diathesis. However, appropriate pre-treatment made it possible recently. We present a case of ureteral stone patient...
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A case report of the hemophilic arthritis

Choi SW, Choi BS

A case report of the hemophilic arthritis, of which incidence is not common. Hemophilia is a constitutional disease characterized by a delayed clotting time of the blood and a lifelong...
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Two Cases of Infant Hemophilia A Patients with Inhibitors

Yu DU, Park JK, Park YS

Development of inhibitors is currently one of the most serious complications of hemophilia treatment. Typically, the propensity to develop an inhibitor is likely influenced by both genetic and non-genetic factors....
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Bone Density Status in Bleeding Disorders: Where Are We and What Needs to Be Done?

Mansouritorghabeh H, Rezaieyazdi Z

Bleeding disorders, including hemophilia, can be seen in every ethnic population in the world. Among various bleeding disorders, reduced bone density has been addressed in hemophilia A. In recent years,...
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Various Complications after a Vascular Procedure in Patients with Hemophilia

Ha YS, Park YS

Hemophilia, an inherited bleeding disorder, is caused by a deficiency of coagulation factor VIII or IX. Most of patients with hemophilia need vascular procedure, which can lead to complications. Even...
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The Adjustment of Patients with Hemophilia

Kim WO

  • KMID: 2291091
  • J Korean Acad Adult Nurs.
  • 2002 Dec;14(4):635-644.
PURPOSE: This research was done to establish a theoretical foundation for the adjustment process of patients with hemophilia. METHOD: For this study, 14 patients with hemophilia participated. The data was...
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Total Knee Arthroplasty-associated Acquired Hemophilia: A Case Report

Song MH, Ahn SJ, Yoo SH, Kim BH, Park JH

  • KMID: 2186782
  • J Korean Orthop Assoc.
  • 2006 Feb;41(1):167-169.
Acquired hemophilia due to the acquisition of antibodies to factor VIII is quite rare, and is associated with conditions such as pregnancy, lymphoma and autoimmune disorders. However, surgical trauma has...
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