-
1
-
-
0029119879
-
An update on clinical and basic aspects of the protein C anticoagulant pathway
-
Esmon CT, Schwarz HP. An update on clinical and basic aspects of the protein C anticoagulant pathway. Trends Cardiovasc Med. 1995;5: 141-148.
-
(1995)
Trends Cardiovasc Med.
, vol.5
, pp. 141-148
-
-
Esmon, C.T.1
Schwarz, H.P.2
-
2
-
-
0019789514
-
Deficiency of protein C in congenital thrombotic disease
-
Griffin JH, Evatt B, Zimmerman TS, Kleiss AJ, Wideman C. Deficiency of protein C in congenital thrombotic disease. J Clin Invest. 1981;68: 1370-1373.
-
(1981)
J Clin Invest.
, vol.68
, pp. 1370-1373
-
-
Griffin, J.H.1
Evatt, B.2
Zimmerman, T.S.3
Kleiss, A.J.4
Wideman, C.5
-
3
-
-
0027390067
-
Protein C deficiency: A database of mutation. For the protein C & S subcommittee of the scientific and standardization committee of the international society on thrombosis and haemostasis
-
Reitsma PH, Poort SR, Bernardi F, Gandrille S, Long GL, Sala N, Cooper DN. Protein C deficiency: A database of mutation. For the protein C & S subcommittee of the scientific and standardization committee of the international society on thrombosis and haemostasis. Thromb Haemost. 1993;69:77-84.
-
(1993)
Thromb Haemost.
, vol.69
, pp. 77-84
-
-
Reitsma, P.H.1
Poort, S.R.2
Bernardi, F.3
Gandrille, S.4
Long, G.L.5
Sala, N.6
Cooper, D.N.7
-
4
-
-
0029033740
-
Protein C deficiency in a controlled series of unselected outpatients: An infrequent but clear risk factor for venous thrombosis
-
Koster T, Rosendaal FR, Briët E, van der Meer FJ, Colly LP, Trienekens PH, Poort SR, Reitsma PH, Vandenbroucke JP. Protein C deficiency in a controlled series of unselected outpatients: An infrequent but clear risk factor for venous thrombosis. Blood. 1995;85:2756-2761.
-
(1995)
Blood
, vol.85
, pp. 2756-2761
-
-
Koster, T.1
Rosendaal, F.R.2
Briët, E.3
Van Der Meer, F.J.4
Colly, L.P.5
Trienekens, P.H.6
Poort, S.R.7
Reitsma, P.H.8
Vandenbroucke, J.P.9
-
5
-
-
0027447258
-
Inherited predisposition to thrombosis
-
Miletich JP, Prescott SM, White R, Majerus PW, Bovill EG. Inherited predisposition to thrombosis. Cell. 1993;72:477-480.
-
(1993)
Cell
, vol.72
, pp. 477-480
-
-
Miletich, J.P.1
Prescott, S.M.2
White, R.3
Majerus, P.W.4
Bovill, E.G.5
-
6
-
-
0027465837
-
Increased risk of venous thrombosis in carriers of hereditary protein C deficiency defect
-
Allaart CF, Poort SR, Rosendaal FR, Reitsma PH, Bertina RM, Briët E. Increased risk of venous thrombosis in carriers of hereditary protein C deficiency defect. Lancet. 1993;341:134-138.
-
(1993)
Lancet
, vol.341
, pp. 134-138
-
-
Allaart, C.F.1
Poort, S.R.2
Rosendaal, F.R.3
Reitsma, P.H.4
Bertina, R.M.5
Briët, E.6
-
7
-
-
0024532084
-
Sublocalization of the human protein C gene on chromosome 2q13-q14
-
Patracchini P, Aiello V, Palazzi P, Calzolari E, Bernardi F. Sublocalization of the human protein C gene on chromosome 2q13-q14. Hum Genet. 1989;81:191-192.
-
(1989)
Hum Genet.
, vol.81
, pp. 191-192
-
-
Patracchini, P.1
Aiello, V.2
Palazzi, P.3
Calzolari, E.4
Bernardi, F.5
-
10
-
-
0028270190
-
Determination of the allelic and haplotype frequencies of three polymorphisms in the promoter region of the human protein C gene
-
Spek CA, Poort SR, Bertina RM, Reitsma PH. Determination of the allelic and haplotype frequencies of three polymorphisms in the promoter region of the human protein C gene. Blood Coag Fibrinol. 1994;5: 309-311.
-
(1994)
Blood Coag Fibrinol.
, vol.5
, pp. 309-311
-
-
Spek, C.A.1
Poort, S.R.2
Bertina, R.M.3
Reitsma, P.H.4
-
11
-
-
0028968010
-
Genotypic variation in the promoter region of the protein C gene is associated with plasma protein C levels and thrombotic risk
-
Spek CA, Koster T, Rosendaal FR, Bertina RM, Reitsma PH. Genotypic variation in the promoter region of the protein C gene is associated with plasma protein C levels and thrombotic risk. Arterioscler Thromb Vasc Biol. 1995;15:214-218.
-
(1995)
Arterioscler Thromb Vasc Biol.
, vol.15
, pp. 214-218
-
-
Spek, C.A.1
Koster, T.2
Rosendaal, F.R.3
Bertina, R.M.4
Reitsma, P.H.5
-
12
-
-
0029059857
-
Polymorphic variation in the human protein C (PROC) gene promoter can influence transcriptional efficiency in vitro
-
Scopes D, Berg LP, Krawczak M, Kakkar VV, Cooper DN. Polymorphic variation in the human protein C (PROC) gene promoter can influence transcriptional efficiency in vitro. Blood Coag Fibrinol 1995;6:317-321.
-
(1995)
Blood Coag Fibrinol
, vol.6
, pp. 317-321
-
-
Scopes, D.1
Berg, L.P.2
Krawczak, M.3
Kakkar, V.V.4
Cooper, D.N.5
-
13
-
-
0029906758
-
First case of sporadic protein S deficiency due to a novel candidate mutation, Ala 484 Pro, in the protein S active gene (PROS 1)
-
Borgel D, Jude B, Aiach M, Gandrille S. First case of sporadic protein S deficiency due to a novel candidate mutation, Ala 484 Pro, in the protein S active gene (PROS 1). Thromb Haemost. 1996;75:883-886.
-
(1996)
Thromb Haemost.
, vol.75
, pp. 883-886
-
-
Borgel, D.1
Jude, B.2
Aiach, M.3
Gandrille, S.4
-
14
-
-
0029000287
-
A rapid screening method for the factor V arg 506 to Gln mutation
-
Gandrille S, Alhenc-Gelas M, Aiach M. A rapid screening method for the factor V Arg 506 to Gln mutation. Blood Coag Fibrinol. 1995;6:245-248.
-
(1995)
Blood Coag Fibrinol.
, vol.6
, pp. 245-248
-
-
Gandrille, S.1
Alhenc-Gelas, M.2
Aiach, M.3
-
15
-
-
0027520285
-
Venous thrombosis due to poor anticoagulant response to activated protein C: Leiden thrombophilia study
-
Koster T, Rosendaal FR, de Ronde H, Briët E, Vandenbroucke JP, Bertina RM. Venous thrombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia Study. Lancet. 1993;342:1503-1506.
-
(1993)
Lancet
, vol.342
, pp. 1503-1506
-
-
Koster, T.1
Rosendaal, F.R.2
De Ronde, H.3
Briët, E.4
Vandenbroucke, J.P.5
Bertina, R.M.6
-
16
-
-
0028098210
-
Resistance to activated protein C as a basis for venous thrombosis
-
Svensson PJ, Dahlbäck B. Resistance to activated protein C as a basis for venous thrombosis. N Engl J Med. 1994;330:517-522.
-
(1994)
N Engl J Med.
, vol.330
, pp. 517-522
-
-
Svensson, P.J.1
Dahlbäck, B.2
-
17
-
-
0029850530
-
A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
-
Poort RS, Rosendaal FR, Reitsma PH, Bertina RM. A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood. 1996;88:3698-3703.
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, R.S.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
18
-
-
0031981017
-
Geographic distribution of the 20210 G to A prothrombin variant
-
Rosendaal FR, Doggen CJM, Zivelin A, Arruda VR, Aiach M, Siscovick DS, Hillarp A, Watzke HH, Bernardi F, Cumming AM, Preston FE, Reitsma PH. Geographic distribution of the 20210 G to A prothrombin variant. Thromb Haemost. 1998;79:706-708.
-
(1998)
Thromb Haemost.
, vol.79
, pp. 706-708
-
-
Rosendaal, F.R.1
Doggen, C.J.M.2
Zivelin, A.3
Arruda, V.R.4
Aiach, M.5
Siscovick, D.S.6
Hillarp, A.7
Watzke, H.H.8
Bernardi, F.9
Cumming, A.M.10
Preston, F.E.11
Reitsma, P.H.12
|