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Quoted phrase not found in phrase index: "Thrombophilia due to protein C deficiency, autosomal dominant"
Page 1
Protein C and protein S deficiency - practical diagnostic issues.
Wypasek E, Undas A. Wypasek E, et al. Adv Clin Exp Med. 2013 Jul-Aug;22(4):459-67. Adv Clin Exp Med. 2013. PMID: 23986205 Free article.
In the presence of PS, phospholipids and calcium, activated PC (APC) inactivates membrane bound factors V (FVa) and FVIIIa by their cleavage at the specific arginine residues. PC and PS deficiencies are inherited as autosomal dominant disorders associated with recur …
In the presence of PS, phospholipids and calcium, activated PC (APC) inactivates membrane bound factors V (FVa) and FVIIIa by their cleavage …
Ischemic stroke due to protein C deficiency.
Kohler J, Kasper J, Witt I, von Reutern GM. Kohler J, et al. Stroke. 1990 Jul;21(7):1077-80. doi: 10.1161/01.str.21.7.1077. Stroke. 1990. PMID: 2195715
Plasma protein C exerts anticoagulatory effects by inactivating factors V and VIII. Hereditary protein C deficiency is transmitted as an autosomal dominant disorder. Homozygous individuals usually develop purpura fulminans as newborns; heterozyg …
Plasma protein C exerts anticoagulatory effects by inactivating factors V and VIII. Hereditary protein C deficiency is …
Resistance to activated protein C as a basis for venous thrombosis.
Svensson PJ, Dahlbäck B. Svensson PJ, et al. N Engl J Med. 1994 Feb 24;330(8):517-22. doi: 10.1056/NEJM199402243300801. N Engl J Med. 1994. PMID: 8302317 Free article.
The inherited nature of the defect was confirmed in a majority of cases, and the family studies suggested the mode of inheritance to be autosomal dominant. The thrombosis-free survival of APC-resistant family members was significantly less than that of non-APC-resis …
The inherited nature of the defect was confirmed in a majority of cases, and the family studies suggested the mode of inheritance to be a …
Incidence and clinical characteristics of hereditary disorders associated with venous thrombosis.
Tabernero MD, Tomas JF, Alberca I, Orfao A, Lopez Borrasca A, Vicente V. Tabernero MD, et al. Am J Hematol. 1991 Apr;36(4):249-54. doi: 10.1002/ajh.2830360405. Am J Hematol. 1991. PMID: 1826407
Their families were studied. In all cases the disorders were inherited as an autosomal dominant trait. The first thrombotic episodes occurred at a age of below 40 years. There was no relationship between protein levels and the occurrence of thrombosis, although a si …
Their families were studied. In all cases the disorders were inherited as an autosomal dominant trait. The first thrombotic ep …
Beta 2-glycoprotein I deficiency and the risk of thrombosis.
Bancsi LF, van der Linden IK, Bertina RM. Bancsi LF, et al. Thromb Haemost. 1992 Jun 1;67(6):649-53. Thromb Haemost. 1992. PMID: 1509404
Therefore we studied the possibility that a hereditary beta 2-GP I deficiency is a risk factor for (familial) thrombophilia. Plasma beta 2-GP I levels were measured in healthy volunteers and four different groups of patients with (familial) thrombophilia. ...The pos …
Therefore we studied the possibility that a hereditary beta 2-GP I deficiency is a risk factor for (familial) thrombophilia. Plasma b …