- A Case of Hemophilia A Diagnosed in a Premature Infant
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Oh KW, Lee KY, Kim JH, Rhee KW, Jeong JY, Park SK
- KMID: 2144478
- J Korean Soc Neonatol.
- 2010 May;17(1):132-135.
Although the majority of abnormal bleeding during the neonatal period results from acquired coagulation disorders, inherited coagulation disorders can also manifest at this time. Hemophilia is the most common of... -
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- Recurrent Acute Pulmonary Embolism Associated With Protein S Deficiency
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Kim SK, Kim SH, Cheon JH, Kim JU, Ko SH, Lee SW
- KMID: 2340258
- J Korean Geriatr Soc.
- 2013 Mar;17(1):55-58.
Pulmonary embolism is a common clinical problem in patients with immobilization, cancer, indwelling central venous catheter and surgery. However, although rare, it may occur in patients with inherited thrombophilia. Protein... -
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- Utilization Patterns of Coagulation Factor Consumption for Patients with Hemophilia
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Lee SO, Yu SY
- KMID: 2359989
- J Korean Med Sci.
- 2016 Jan;31(1):33-38.
- doi: 10.3346/jkms.2016.31.1.33
Hemophilia is a serious rare disease that requires continuous management and treatment for which the medicine is costly at the annual average of 100 million KRW for an individual. The... -
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- A Case of Neonatal Purpura Fulminans Due to a Homozygous Protein C Deficiency
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Jo JH, Oh CK, Kim MB, Jang HS, Kwon KS
- KMID: 2146438
- Korean J Dermatol.
- 2002 Jan;40(1):38-43.
Homozygous protein C deficiency is a rare hereditary coagulation disorder that occurs most often in childhood and is characterized by widespread thrombosis of capillaries and venules, abrupt onset of ecchymoses... -
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- Hemophilia A in a Senior Patient: A Case Report of Spinal Epidural Hematoma as First Presentation
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Ahn DK, Jung WS, Lee JI
- KMID: 2270147
- Asian Spine J.
- 2015 Jun;9(3):452-455.
- doi: 10.4184/asj.2015.9.3.452
Hemophilia A is a hereditary coagulation disorder. Most cases are diagnosed at birth or at least during childhood. A spontaneous spinal epidural hematoma was developed in a 74-year-old male patient... -
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- Fibrinogen Yecheon: Congenital Dysfibrinogenemia with Gamma Methionine-310 to Threonine Substitution
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Park E, Park G, Park R, Kim HJ, Lee SJ, Cha YJ
- KMID: 1783157
- J Korean Med Sci.
- 2009 Dec;24(6):1203-1206.
- doi: 10.3346/jkms.2009.24.6.1203
This case study reports a rare fibrinogen variant, gamma Met310Thr mutation, for the first time in Korea. The case shows a point mutation from T to C in the 1,007th... -
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