Congenital Hypofibrinogenemia Detected during Preoperative Workup for Major Cardiac Surgery
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K. Kumar | K. Chetak | K. Sujay | U. Kumar | V. Hiremath
[1] A. Iorio,et al. Thrombosis in Inherited Fibrinogen Disorders , 2017, Transfusion Medicine and Hemotherapy.
[2] Q. Ding,et al. Clinical features and molecular basis of 102 Chinese patients with congenital dysfibrinogenemia. , 2015, Blood cells, molecules & diseases.
[3] D. Agrawal,et al. Hypofibrinogenemia in isolated traumatic brain injury in Indian patients. , 2010, Neurology India.
[4] M. Verhovsek,et al. Laboratory testing for fibrinogen abnormalities , 2008, American journal of hematology.
[5] S. Acharya,et al. Rare inherited disorders of fibrinogen , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.
[6] R. Gopinath,et al. An unusual cause of a prolonged activated coagulation time during cardiac surgery: congenital hypofibrinogenemia. , 2008, Journal of cardiothoracic and vascular anesthesia.
[7] S. Duga,et al. The molecular basis of quantitative fibrinogen disorders , 2006, Journal of thrombosis and haemostasis : JTH.
[8] H. Yapıcıoğlu,et al. Congenital Hypofibrinogenemia: A Newborn Infant with Cord Bleeding. , 2000, Turkish journal of haematology : official journal of Turkish Society of Haematology.
[9] J. Minnis,et al. Congenital heart disease associated with congenital hypofibrinogenemia. Report of a case subjected to corrective surgery. , 1961, The American journal of cardiology.