Arterial thrombosis as clinical manifestation of congenital protein C deficiency

Annals of Hematology

Volumn 62, Issue 5, 1991, Pages 180-183

  De Stefano, V ^a   Leone, G ^a   Micalizzi, P ^a   Teofili, L ^a   Falappa, P G ^a,b   Pollari, G ^a,c   Bizzi, B ^a  

^a CATHOLIC UNIVERSITY   (Italy)

^b Istituto di Radiologia di Universita Cattolica del Sacro Cuore di Roma   (Italy)

^c SAN GIOVANNI ADDOLORATA HOSPITAL   (Italy)

Author keywords

Arterial thrombosis; Congenital protein C deficiency; Myocardial infarction; TIA

Indexed keywords

ACETYLSALICYLIC ACID; DIPYRIDAMOLE; PROTEIN C; STANOZOLOL;

ADULT; ARTICLE; CLINICAL ARTICLE; FEMALE; HEART INFARCTION; HUMAN; MALE; PRIORITY JOURNAL; PROTEIN DEFICIENCY; THROMBOSIS; TRANSIENT ISCHEMIC ATTACK;

ADULT; CAROTID ARTERY THROMBOSIS; CASE REPORT; HETEROZYGOTE; HUMAN; ISCHEMIC ATTACK, TRANSIENT; MALE; MIDDLE AGE; MYOCARDIAL INFARCTION; PROTEIN C; PROTEIN C DEFICIENCY; THROMBOPHLEBITIS;

EID: 0025892747     PISSN: 09395555     EISSN: 14320584     Source Type: Journal    
DOI: 10.1007/BF01703145     Document Type: Article

References (31)

1. Hereditary dysfunctional protein C (protein C Bergamo)
2. The clinical spectrum of heterozygous protein C deficiency in a large New England kindred
3. Hereditary protein C deficiency
4. Hereditary protein C deficiency
5. The regulation of haemostasis: the protein C system
6. Protein C in acute stroke
7. Transient ischemic attack in a patient with congenital protein C deficiency during treatment with stanazolol
8. Factor X Roma: a congenital factor X variant defective at different degrees in the intrinsic and the extrinsic activation
9. Association of congenital protein C deficiency and latent myeloproliferative disease as cause of splanchnic venous thrombosis in a 34-year-old woman
10. Mesenteric vein thrombosis in protein S congenital deficiency
11. Association of inherited dysfibrinogenaemia and protein C deficiency in two unrelated families
12. Severe arterial cerebral thrombosis in a patient with protein S deficiency (moderately reduced total and markedly reduced free protein S): a family study
13. The frequency of type-I heterozygous protein S and protein C deficiency in 141 unrelated young patients with venous thrombosis
14. Deficiency of protein C in congenital thrombotic state
15. Congenital protein C deficiency and thrombotic disease in nine French families
16. Incidence, prevalence, and mortality of cardiovascular diseases
17. Heterozygous protein C deficiency type I
18. Antithrombin III Pescara: a defective AT III variant with no alterations of plasma-crossed immunoelectrophoresis but with an abnormal crossed immunoelectrofocusing pattern
19. Recurrent thrombophlebitis due to protein C deficiency after splenectomy for immune thrombocytopenic purpura
20. Absence of thrombosis in subjects with heterozygous hereditary protein C deficiency
21. Maladie thromboembolique veineuse et artérielle familiale par déficit en protéine
22. Recurrent multiplebranch retinal arteriolar occlusions in a patient with protein C deficiency
23. Protein C: an automated activity assay
24. Clinical relevance of protein C
25. Protein C deficiency in two Austrian families
26. Homozygous protein C deficiency with moderately severe clinical symptoms
27. Arterial thrombosis and protein S deficiency
28. Protein C deficiency: a cause of amaurosis fugax?
29. Homozygous protein C deficiency with delayed onset of symptoms at 7 to 10 months
30. Portal vein thrombosis with ruptured oesophageal varices as presenting manifestation of hereditary protein C deficiency
31. Transient ischemic attack (TIA) in a patient with non-thrombogenic hereditary protein C deficiency under oral contraceptives