-
1
-
-
47249084343
-
Advances in understanding pathogenic mechanisms of thrombophilic disorders
-
B. Dahlbäck Advances in understanding pathogenic mechanisms of thrombophilic disorders Blood 112 2008 19 27
-
(2008)
Blood
, vol.112
, pp. 19-27
-
-
Dahlbäck, B.1
-
2
-
-
67149089651
-
Selective testing for thrombophilia in patients with first venous thrombosis: Results from a retrospective family cohort study on absolute thrombotic risk for currently known thrombophilic defects in 2479 relatives
-
W.M. Lijfering, J.L. Brouwer, N.J. Veeger, I. Bank, M. Coppens, and S. Middeldorp Selective testing for thrombophilia in patients with first venous thrombosis: results from a retrospective family cohort study on absolute thrombotic risk for currently known thrombophilic defects in 2479 relatives Blood 113 2009 5314 5322
-
(2009)
Blood
, vol.113
, pp. 5314-5322
-
-
Lijfering, W.M.1
Brouwer, J.L.2
Veeger, N.J.3
Bank, I.4
Coppens, M.5
Middeldorp, S.6
-
3
-
-
77954510728
-
A prospective cohort study on the absolute risks of venous thromboembolism and predictive value of screening asymptomatic relatives of patients with hereditary deficiencies of protein S, protein C or antithrombin
-
B.K. Mahmoodi, J.L. Brouwer, M.K. Ten Kate, W.M. Lijfering, N.J. Veeger, and A.B. Mulder A prospective cohort study on the absolute risks of venous thromboembolism and predictive value of screening asymptomatic relatives of patients with hereditary deficiencies of protein S, protein C or antithrombin J Thromb Haemost 8 2010 1193 1200
-
(2010)
J Thromb Haemost
, vol.8
, pp. 1193-1200
-
-
Mahmoodi, B.K.1
Brouwer, J.L.2
Ten Kate, M.K.3
Lijfering, W.M.4
Veeger, N.J.5
Mulder, A.B.6
-
4
-
-
84865788776
-
Low borderline plasma levels of antithrombin, protein C and protein S are risk factors for venous thromboembolism
-
P. Bucciarelli, S.M. Passamonti, E. Biguzzi, F. Gianniello, F. Franchi, and P.M. Mannucci Low borderline plasma levels of antithrombin, protein C and protein S are risk factors for venous thromboembolism J Thromb Haemost 10 2012 1783 1791
-
(2012)
J Thromb Haemost
, vol.10
, pp. 1783-1791
-
-
Bucciarelli, P.1
Passamonti, S.M.2
Biguzzi, E.3
Gianniello, F.4
Franchi, F.5
Mannucci, P.M.6
-
5
-
-
0030951829
-
Laboratory evaluation and clinical characteristics of 2,132 consecutive unselected patients with venous thromboembolism-results of the Spanish Multicentric Study on Thrombophilia (EMET-Study)
-
J. Mateo, A. Oliver, M. Borrell, N. Sala, and J. Fontcuberta Laboratory evaluation and clinical characteristics of 2,132 consecutive unselected patients with venous thromboembolism-results of the Spanish Multicentric Study on Thrombophilia (EMET-Study) Thromb Haemost 77 1997 444 451
-
(1997)
Thromb Haemost
, vol.77
, pp. 444-451
-
-
Mateo, J.1
Oliver, A.2
Borrell, M.3
Sala, N.4
Fontcuberta, J.5
-
6
-
-
34548723892
-
Arterial thrombosis and the role of thrombophilia
-
S.M. Boekholdt, and M.H. Kramer Arterial thrombosis and the role of thrombophilia Semin Thromb Hemost 33 2007 588 596
-
(2007)
Semin Thromb Hemost
, vol.33
, pp. 588-596
-
-
Boekholdt, S.M.1
Kramer, M.H.2
-
7
-
-
84929510353
-
Antithrombin Heparin Binding Site deficiency: A challenging diagnosis of a not so benign thrombophilia
-
C. Orlando, O. Heylen, W. Lissens, and K. Jochmans Antithrombin Heparin Binding Site deficiency: a challenging diagnosis of a not so benign thrombophilia Thromb Res 135 2015 1179 1185
-
(2015)
Thromb Res
, vol.135
, pp. 1179-1185
-
-
Orlando, C.1
Heylen, O.2
Lissens, W.3
Jochmans, K.4
-
8
-
-
0025253620
-
Antithrombin III activity in healthy blood donors: Age and sex related changes and prevalence of asymptomatic deficiency
-
R.C. Tait, I.D. Walker, J.F. Davidson, S.I. Islam, and R. Mitchell Antithrombin III activity in healthy blood donors: age and sex related changes and prevalence of asymptomatic deficiency Br J Haematol 75 1990 141 142
-
(1990)
Br J Haematol
, vol.75
, pp. 141-142
-
-
Tait, R.C.1
Walker, I.D.2
Davidson, J.F.3
Islam, S.I.4
Mitchell, R.5
-
9
-
-
34247560260
-
Detecting antithrombin deficiency may be a difficult task-more than one test is necessary
-
S.R. Kristensen, B. Rasmussen, S. Pedersen, and L. Bathum Detecting antithrombin deficiency may be a difficult task-more than one test is necessary J Thromb Haemost 5 2007 617 618
-
(2007)
J Thromb Haemost
, vol.5
, pp. 617-618
-
-
Kristensen, S.R.1
Rasmussen, B.2
Pedersen, S.3
Bathum, L.4
-
10
-
-
84922432954
-
Development of a novel, rapid assay for detection of heparin-binding defect antithrombin deficiencies: The heparin-antithrombin binding (HAB) ratio
-
G.W. Moore, N. de Jager, and J.A. Cutler Development of a novel, rapid assay for detection of heparin-binding defect antithrombin deficiencies: the heparin-antithrombin binding (HAB) ratio Thromb Res 135 2015 161 166
-
(2015)
Thromb Res
, vol.135
, pp. 161-166
-
-
Moore, G.W.1
De Jager, N.2
Cutler, J.A.3
-
11
-
-
84881313980
-
Great discrepancy in antithrombin activity measured using five commercially available functional assays
-
K. Javela, S. Engelbarth, L. Hiltunen, P. Mustonen, and M. Puurunen Great discrepancy in antithrombin activity measured using five commercially available functional assays Thromb Res 132 2013 132 137
-
(2013)
Thromb Res
, vol.132
, pp. 132-137
-
-
Javela, K.1
Engelbarth, S.2
Hiltunen, L.3
Mustonen, P.4
Puurunen, M.5
-
12
-
-
84885347863
-
Type II antithrombin deficiency caused by a founder mutation Pro73Leu in the Finnish population: Clinical picture
-
M. Puurunen, P. Salo, S. Engelbarth, K. Javela, and M. Perola Type II antithrombin deficiency caused by a founder mutation Pro73Leu in the Finnish population: clinical picture J Thromb Haemost 11 2013 1844 1849
-
(2013)
J Thromb Haemost
, vol.11
, pp. 1844-1849
-
-
Puurunen, M.1
Salo, P.2
Engelbarth, S.3
Javela, K.4
Perola, M.5
-
13
-
-
34248350430
-
Antithrombin Cambridge II (A384S): An underestimated genetic risk factor for venous thrombosis
-
J. Corral, D. Hernandez-Espinosa, J.M. Soria, R. Gonzalez-Conejero, A. Ordonez, and J.R. Gonzalez-Porras Antithrombin Cambridge II (A384S): an underestimated genetic risk factor for venous thrombosis Blood 109 2007 4258 4263
-
(2007)
Blood
, vol.109
, pp. 4258-4263
-
-
Corral, J.1
Hernandez-Espinosa, D.2
Soria, J.M.3
Gonzalez-Conejero, R.4
Ordonez, A.5
Gonzalez-Porras, J.R.6
-
14
-
-
79954756912
-
The phenotypic and genetic assessment of antithrombin deficiency
-
P.C. Cooper, F. Coath, M.E. Daly, and M. Makris The phenotypic and genetic assessment of antithrombin deficiency Int J Lab Hematol 33 2011 227 237
-
(2011)
Int J Lab Hematol
, vol.33
, pp. 227-237
-
-
Cooper, P.C.1
Coath, F.2
Daly, M.E.3
Makris, M.4
-
15
-
-
0037085777
-
Discrepancy between antithrombin activity methods revealed in Antithrombin Stockholm: Do factor Xa-based methods overestimate antithrombin activity in some patients?
-
J.S. Ungerstedt, S. Schulman, N. Egberg, J. Antovic, and N. Blombäck Discrepancy between antithrombin activity methods revealed in Antithrombin Stockholm: do factor Xa-based methods overestimate antithrombin activity in some patients? Blood 99 2002 2271 2272
-
(2002)
Blood
, vol.99
, pp. 2271-2272
-
-
Ungerstedt, J.S.1
Schulman, S.2
Egberg, N.3
Antovic, J.4
Blombäck, N.5
-
16
-
-
0027999955
-
Thromboembolic disease due to thermolabile conformational changes of antithrombin Rouen-VI (187 Asn- > Asp)
-
D. Bruce, D.J. Perry, J.Y. Borg, R.W. Carrell, and M.R. Wardell Thromboembolic disease due to thermolabile conformational changes of antithrombin Rouen-VI (187 Asn- > Asp) J Clin Invest 94 1994 2265 2274
-
(1994)
J Clin Invest
, vol.94
, pp. 2265-2274
-
-
Bruce, D.1
Perry, D.J.2
Borg, J.Y.3
Carrell, R.W.4
Wardell, M.R.5
-
17
-
-
0032532347
-
Antithrombins Wibble and Wobble (T85M/K): Archetypal conformational diseases with in vivo latent-transition, thrombosis, and heparin activation
-
N.J. Beauchamp, R.N. Pike, M. Daly, L. Butler, M. Makris, and T.R. Dafforn Antithrombins Wibble and Wobble (T85M/K): archetypal conformational diseases with in vivo latent-transition, thrombosis, and heparin activation Blood 92 1998 2696 2706
-
(1998)
Blood
, vol.92
, pp. 2696-2706
-
-
Beauchamp, N.J.1
Pike, R.N.2
Daly, M.3
Butler, L.4
Makris, M.5
Dafforn, T.R.6
-
18
-
-
84871052208
-
Congenital disorder of glycosylation (PMM2-CDG) in a patient with antithrombin deficiency and severe thrombophilia
-
M.E. de la Morena-Barrio, T.S. Sevivas, I. Martinez-Martinez, A. Miñano, V. Vicente, and J. Jaeken Congenital disorder of glycosylation (PMM2-CDG) in a patient with antithrombin deficiency and severe thrombophilia J Thromb Haemost 10 2012 2625 2627
-
(2012)
J Thromb Haemost
, vol.10
, pp. 2625-2627
-
-
De La Morena-Barrio, M.E.1
Sevivas, T.S.2
Martinez-Martinez, I.3
Miñano, A.4
Vicente, V.5
Jaeken, J.6
-
19
-
-
62549106201
-
Antithrombin Cambridge II (A384S) supports a role for antithrombin deficiency in arterial thrombosis
-
V. Roldán, A. Ordoñez, F. Marín, E. Zorio, J.M. Soria, and A. Miñano Antithrombin Cambridge II (A384S) supports a role for antithrombin deficiency in arterial thrombosis Thromb Haemost 101 2009 483 486
-
(2009)
Thromb Haemost
, vol.101
, pp. 483-486
-
-
Roldán, V.1
Ordoñez, A.2
Marín, F.3
Zorio, E.4
Soria, J.M.5
Miñano, A.6
|