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References

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    White, GC, Rosendaal, F, Aledort, LM, Lusher, JM, Rothschild, C, Ingerslev, J. Definitions in Hemophilia. Recommendations of the Scientific Subcommittee on FVIII and Factor IX of the SSC of ISTH. Thromb Haemost 2001; 0: 560.
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    Preston, FE, Kitchen, S. Quality control and FVIII assays. Haemophilia 1998; 4: 6513.
  • 3
    Rizza, CR. Haemophilia and related inherited coagulation defects. In: Bloom, AL, Forbes, CD, Thomas, DP, Tuddenham, EGD, eds. Haemostasis and Thrombosis, 3rd edn. Edinburgh: Churchill Livingstone, 1994: 81941.
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    Brettler, DB, Levine, PH. Clinical manifestations and therapy of inherited coagulation factor deficiencies. In: Coleman, RW, Hirsh, J, Mader, VJ, Saltzman, EW, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice, 3rd edn. Philadephia: J P Lippincott Co., 1994: 16983.
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    Arun, B, Kessler, CM. Clinical manifestations and therapy of the haemophilias. In: Coleman, RW, Hirsh, J, Mader, VJ, Clowes, AW, George, JN, eds. Hemostasis and Thrombosis: Basic Principles and Clinical Practice. Inherited Hemorrhagic Disorders, 4th edn. Philadelphia: J P Lippincott, Williams & Wilkins, 2001: 81524.
  • 6
    The Haemophilia Alliance National Service Specification, Service Standards and Deliveries. Types of haemophilia. http://www.haemophiliaalliance.org.uk 2001.