The role of abnormalities in the anticoagulant and fibrinolytic systems in retinal vascular occlusions.
暂无分享,去创建一个
[1] S. Thorsen,et al. A family with reduced plasminogen activator activity in blood associated with recurrent venous thrombosis. , 2009, Scandinavian journal of haematology.
[2] I. Nilsson,et al. A family with thromboembolic disease associated with deficient fibrinolytic activity in vessel wall. , 2009, Acta medica Scandinavica.
[3] B. Furie,et al. Molecular and cellular biology of blood coagulation. , 1992, The New England journal of medicine.
[4] H. Büller,et al. Deficiencies of coagulation-inhibiting and fibrinolytic proteins in outpatients with deep-vein thrombosis. , 1990, The New England journal of medicine.
[5] P. Sibony,et al. Protein S deficiency associated with central retinal artery occlusion. , 1990, Archives of ophthalmology.
[6] L. Pasquale,et al. Dural sinus thrombosis with abnormalities of protein S and fibrinogen. , 1990, A M A Archives of Ophthalmology.
[7] G. Coscas,et al. Increased red blood cell aggregation in retinal vein occlusion , 1990, British journal of haematology.
[8] D. Tollefsen. Laboratory Diagnosis of Antithrombin and Heparin Cofactor II Deficiency , 1990, Seminars in thrombosis and hemostasis.
[9] C. Chesterman,et al. Anticardiolipin antibodies and lupus anticoagulants comprise separate antibody subgroups with different phospholipid binding characteristics , 1989, British journal of haematology.
[10] A. Patz,et al. Vaso-occlusive retinopathy associated with antiphospholipid antibodies (lupus anticoagulant retinopathy). , 1989, Ophthalmology.
[11] J. Brandt,et al. RELATIONSHIP BETWEEN LUPUS ANTICOAGULANTS AND ANTIBODIES TO PHOSPHOLIPID , 1988, Thrombosis and Haemostasis.
[12] J. Nishioka,et al. Plasma protein S activity measured using Protac, a snake venom derived activator of protein C. , 1988, Thrombosis research.
[13] S. Rahimtoola,et al. Changes in blood rheology in patients with stable angina pectoris as a result of coronary artery disease. , 1987, Circulation.
[14] P. Mannucci,et al. Laboratory Screening of Inherited Thrombotic Syndromes , 1987, Thrombosis and Haemostasis.
[15] R. Bertina,et al. Hereditary Heparin Cofactor II Deficiency and the Risk of Development of Thrombosis , 1987, Thrombosis and Haemostasis.
[16] D. Smith,et al. Protein C deficiency: a cause of amaurosis fugax? , 1987, Journal of neurology, neurosurgery, and psychiatry.
[17] G. Hughes,et al. Thrombosis, recurrent fetal loss, and thrombocytopenia. Predictive value of the anticardiolipin antibody test. , 1986, Archives of internal medicine.
[18] K. Stocker,et al. Fast functional protein C assay using Protac, a novel protein C activator. , 1986, Thrombosis research.
[19] P. Comp,et al. The regulation of hemostasis: the protein C system. , 1986, The New England journal of medicine.
[20] F. Kunz,et al. Retinaler Gefäßverschluß bei Antithrombin III-Mangel , 1985 .
[21] G. Hughes,et al. The anticardiolipin syndrome. , 1985, The Journal of rheumatology.
[22] B. Boneu,et al. CONSTITUTIONAL HEPARIN CO-FACTOR II DEFICIENCY ASSOCIATED WITH RECURRENT THROMBOSIS , 1985, The Lancet.
[23] G. Marbet,et al. ASSOCIATION OF HEREDITARY HEPARIN CO-FACTOR II DEFICIENCY WITH THROMBOSIS , 1985, The Lancet.
[24] L. Tengborn,et al. Two different mechanisms in patients with venous thrombosis and defective fibrinolysis: low concentration of plasminogen activator or increased concentration of plasminogen activator inhibitor. , 1985 .
[25] C. Esmon,et al. Familial protein S deficiency is associated with recurrent thrombosis. , 1984, The Journal of clinical investigation.
[26] B. Dahlbäck. Interaction Between Vitamin K-Dependent Protein S and the Complement Protein, C4b-Binding Protein , 1984, Seminars in thrombosis and hemostasis.
[27] R. Bertina,et al. The Use of a Functional and Immunologic Assay for Plasma Protein C in the Study of the Heterogeneity of Congenital Protein C Deficiency , 1984, Thrombosis and Haemostasis.
[28] J. Katz,et al. INHERITED PROTEIN C DEFICIENCY AND COUMARIN-RESPONSIVE CHRONIC RELAPSING PURPURA FULMINANS IN A NEWBORN INFANT , 1983, The Lancet.
[29] J. Soria,et al. Plasminogen Paris I: congenital abnormal plasminogen and its incidence in thrombosis. , 1983, Thrombosis research.
[30] E. Mullaart,et al. A Simple, Sensitive Spectrophotometric Assay for Extrinsic (Tissue-Type) Plasminogen Activator Applicable to Measurements in Plasma , 1982, Thrombosis and Haemostasis.
[31] K. Robbins,et al. Human Plasminogen Variant Chicago III , 1982, Thrombosis and Haemostasis.
[32] J. Griffin,et al. Deficiency of protein C in congenital thrombotic disease. , 1981, The Journal of clinical investigation.
[33] L. Kowal,et al. Abnormal fibrinolysis in retinal vein occlusion. , 1981, Australian journal of ophthalmology.
[34] K. Gohchi,et al. Abnormal plasminogen, a case of recurrent thrombosis. , 1981, Thrombosis research.
[35] K. Robbins,et al. Physiological activation of the human fibrinolytic system. Isolation and characterization of human plasminogen variants, Chicago I and Chicago II. , 1979, The Journal of biological chemistry.
[36] Cosgriff Tm,et al. Central retinal vein occlusion in a patient with familial antithrombin III deficiency: case report. , 1979, Annals of Ophthalmology.
[37] Y. Sakata,et al. Abnormal plasminogen. A hereditary molecular abnormality found in a patient with recurrent thrombosis. , 1978, The Journal of clinical investigation.
[38] M. Pandolfi,et al. COAGULATION AND FlBRlNOLYTlC STUDIES IN 23 PATIENTS WITH OCCLUSION OF THE RETINAL VESSELS , 1972, Acta ophthalmologica.
[39] M. Pandolfi. Fibrinolytic activity of retinal vessels in man and monkey. , 1967, American journal of ophthalmology.
[40] Greiner Ac,et al. Schizophrenia-melanosis: cause or side-effect? , 1965 .
[41] O. Egeberg. Inherited Antithrombin Deficiency Causing Thrombophilia , 1965, Thrombosis and Haemostasis.
[42] C. Greven,et al. Protein S deficiency and bilateral branch retinal artery occlusion. , 1991, Ophthalmology.
[43] M. Samama,et al. Incidence of thromboembolism in association with congenital disorders in coagulation and fibrinolysis. , 1988, Acta chirurgica Scandinavica. Supplementum.
[44] J. Soria,et al. CONGENITAL DYSFIBRINOGENEMIA AND THROMBOSIS , 1988 .
[45] Triplett Da,et al. Clinical application of a functional assay for protein C. , 1987 .
[46] A. Neetens,et al. Bilateral retinal branch vein occlusion in protein C deficiency. , 1987, Bulletin de la Societe belge d'ophtalmologie.
[47] A. Girolami,et al. Fibrinolytic behavior in long-standing branch retinal vein occlusion. , 1987, Ophthalmic Research.
[48] D. Collen. Report of the Meeting of the Subcommittee on Fibrinolysis, Jerusalem, Israel, June 2,1986 , 1986, Thrombosis and Haemostasis.
[49] R. Bertina,et al. Prevalence of protein C (PC) and protein S (PS) deficiency in patients with thrombotic disease , 1986 .
[50] S. Pizzo,et al. Venous thrombosis in a family with defective release of vascular plasminogen activator and elevated plasma factor VIII/von Willebrand's factor. , 1983, The American journal of medicine.
[51] H. Heidrich,et al. Retinal vascular occlusion and thrombocyte aggregation. , 1980, Journal of medicine.
[52] Priluck Ia. Impending central retinal vein occlusion associated with increased platelet aggregability. , 1979 .
[53] I. Nilsson,et al. Plasminogen Activator Release After Venous Occlusion and Infusion of DDAVP , 1977, Thrombosis and Haemostasis.
[54] R. Sykes. Letter: Kwashiorkor and tuberculosis. , 1974, Lancet.