-
2
-
-
84926150235
-
Rare bleeding disorders: Diagnosis and treatment
-
R. Palla, F. Peyvandi, and A.D. Shapiro Rare bleeding disorders: diagnosis and treatment Blood 125 13 2015 2052 2061
-
(2015)
Blood
, vol.125
, Issue.13
, pp. 2052-2061
-
-
Palla, R.1
Peyvandi, F.2
Shapiro, A.D.3
-
3
-
-
84930503578
-
Dysfibrinogenemia: From molecular anomalies to clinical manifestations and management
-
A. Casini, M. Neerman-Arbez, R.A. Ariens, and et al. Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management J. Thromb. Haemost. 13 6 2015 909 919
-
(2015)
J. Thromb. Haemost.
, vol.13
, Issue.6
, pp. 909-919
-
-
Casini, A.1
Neerman-Arbez, M.2
Ariens, R.A.3
-
4
-
-
84876458886
-
Mechanisms of fibrin polymerization and clinical implications
-
J.W. Weisel, and R.I. Litvinov Mechanisms of fibrin polymerization and clinical implications Blood 121 10 2013 1712 1719
-
(2013)
Blood
, vol.121
, Issue.10
, pp. 1712-1719
-
-
Weisel, J.W.1
Litvinov, R.I.2
-
5
-
-
84922426328
-
Natural history of patients with congenital dysfibrinogenemia
-
A. Casini, M. Blondon, A. Lebreton, and et al. Natural history of patients with congenital dysfibrinogenemia Blood 125 3 2015 553 561
-
(2015)
Blood
, vol.125
, Issue.3
, pp. 553-561
-
-
Casini, A.1
Blondon, M.2
Lebreton, A.3
-
6
-
-
0028877613
-
Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommittee on Fibrinogen
-
F. Haverkate, and M. Samama Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommittee on Fibrinogen Thromb. Haemost. 73 1 1995 151 161
-
(1995)
Thromb. Haemost.
, vol.73
, Issue.1
, pp. 151-161
-
-
Haverkate, F.1
Samama, M.2
-
7
-
-
84903767898
-
Fibrin clot properties and their modulation in thrombotic disorders
-
A. Undas Fibrin clot properties and their modulation in thrombotic disorders Thromb. Haemost. 112 1 2014 32 42
-
(2014)
Thromb. Haemost.
, vol.112
, Issue.1
, pp. 32-42
-
-
Undas, A.1
-
8
-
-
84908529859
-
Clot properties and cardiovascular disease
-
K.I. Bridge, H. Philippou, and R. Ariens Clot properties and cardiovascular disease Thromb. Haemost. 112 5 2014 901 908
-
(2014)
Thromb. Haemost.
, vol.112
, Issue.5
, pp. 901-908
-
-
Bridge, K.I.1
Philippou, H.2
Ariens, R.3
-
9
-
-
84880620943
-
Fibrin(ogen) and thrombotic disease
-
R.A. Ariens Fibrin(ogen) and thrombotic disease J. Thromb. Haemost. 11 Suppl. 1 2013 294 305
-
(2013)
J. Thromb. Haemost.
, vol.11
, pp. 294-305
-
-
Ariens, R.A.1
-
10
-
-
84904305313
-
Abnormal plasma clot structure and stability distinguish bleeding risk in patients with severe factor XI deficiency
-
M. Zucker, U. Seligsohn, O. Salomon, and et al. Abnormal plasma clot structure and stability distinguish bleeding risk in patients with severe factor XI deficiency J. Thromb. Haemost. 12 7 2014 1121 1130
-
(2014)
J. Thromb. Haemost.
, vol.12
, Issue.7
, pp. 1121-1130
-
-
Zucker, M.1
Seligsohn, U.2
Salomon, O.3
-
11
-
-
0020596374
-
A new type of congenital dysfibrinogenaemia with defective fibrin lysis - Dusard syndrome: Possible relation to thrombosis
-
J. Soria, C. Soria, and P. Caen A new type of congenital dysfibrinogenaemia with defective fibrin lysis - Dusard syndrome: possible relation to thrombosis Br. J. Haematol. 53 4 1983 575 586
-
(1983)
Br. J. Haematol.
, vol.53
, Issue.4
, pp. 575-586
-
-
Soria, J.1
Soria, C.2
Caen, P.3
-
12
-
-
77955463375
-
Functional characterisation of plasma fibrin clots in Polish carriers of fibrinogen gammaArg275His mutation (fibrinogen Zabrze)
-
A. Undas, M. Pastuszczak, T. Iwaniec, and et al. Functional characterisation of plasma fibrin clots in Polish carriers of fibrinogen gammaArg275His mutation (fibrinogen Zabrze) Thromb. Haemost. 104 2 2010 415 417
-
(2010)
Thromb. Haemost.
, vol.104
, Issue.2
, pp. 415-417
-
-
Undas, A.1
Pastuszczak, M.2
Iwaniec, T.3
-
13
-
-
84908173357
-
Two novel mutations in the fibrinogen gamma nodule
-
R. Kotlin, O. Pastva, J. Stikarova, and et al. Two novel mutations in the fibrinogen gamma nodule Thromb. Res. 134 4 2014 901 908
-
(2014)
Thromb. Res.
, vol.134
, Issue.4
, pp. 901-908
-
-
Kotlin, R.1
Pastva, O.2
Stikarova, J.3
-
14
-
-
5644228617
-
A novel mutation (deletion of Aalpha-Asn 80) in an abnormal fibrinogen: Fibrinogen Caracas VI. Consequences of disruption of the coiled coil for the polymerization of fibrin: Peculiar clot structure and diminished stiffness of the clot
-
R.C. Marchi, M.H. Meyer, N.B. de Bosch, and et al. A novel mutation (deletion of Aalpha-Asn 80) in an abnormal fibrinogen: fibrinogen Caracas VI. Consequences of disruption of the coiled coil for the polymerization of fibrin: peculiar clot structure and diminished stiffness of the clot Blood Coagul. Fibrinolysis 15 7 2004 559 567
-
(2004)
Blood Coagul. Fibrinolysis
, vol.15
, Issue.7
, pp. 559-567
-
-
Marchi, R.C.1
Meyer, M.H.2
De Bosch, N.B.3
-
15
-
-
33746602187
-
A classification of the fibrin network structures formed from the hereditary dysfibrinogens
-
T. Sugo, H. Endo, M. Matsuda, and et al. A classification of the fibrin network structures formed from the hereditary dysfibrinogens J. Thromb. Haemost. 4 8 2006 1738 1746
-
(2006)
J. Thromb. Haemost.
, vol.4
, Issue.8
, pp. 1738-1746
-
-
Sugo, T.1
Endo, H.2
Matsuda, M.3
-
17
-
-
77956493323
-
ISTH/SSC bleeding assessment tool: A standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders
-
F. Rodeghiero, A. Tosetto, T. Abshire, and et al. ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders J. Thromb. Haemost. 8 9 2010 2063 2065
-
(2010)
J. Thromb. Haemost.
, vol.8
, Issue.9
, pp. 2063-2065
-
-
Rodeghiero, F.1
Tosetto, A.2
Abshire, T.3
-
18
-
-
0034254319
-
The factor XIII V34L polymorphism accelerates thrombin activation of factor XIII and affects cross-linked fibrin structure
-
R.A. Ariens, H. Philippou, C. Nagaswami, and et al. The factor XIII V34L polymorphism accelerates thrombin activation of factor XIII and affects cross-linked fibrin structure Blood 96 3 2000 988 995
-
(2000)
Blood
, vol.96
, Issue.3
, pp. 988-995
-
-
Ariens, R.A.1
Philippou, H.2
Nagaswami, C.3
-
19
-
-
36349025816
-
Heritability of clot formation, morphology, and lysis: The EuroCLOT study
-
A.M. Carter, C.M. Cymbalista, T.D. Spector, and et al. Heritability of clot formation, morphology, and lysis: the EuroCLOT study Arterioscler. Thromb. Vasc. Biol. 27 12 2007 2783 2789
-
(2007)
Arterioscler. Thromb. Vasc. Biol.
, vol.27
, Issue.12
, pp. 2783-2789
-
-
Carter, A.M.1
Cymbalista, C.M.2
Spector, T.D.3
-
20
-
-
84866843534
-
An international study on the standardization of fibrin clot permeability measurement: Methodological considerations and implications for healthy control values
-
M. Pieters, A. Undas, R. Marchi, and et al. An international study on the standardization of fibrin clot permeability measurement: methodological considerations and implications for healthy control values J. Thromb. Haemost. 10 10 2012 2179 2181
-
(2012)
J. Thromb. Haemost.
, vol.10
, Issue.10
, pp. 2179-2181
-
-
Pieters, M.1
Undas, A.2
Marchi, R.3
-
21
-
-
84899748941
-
Roles of fibrin alpha- and gamma-chain specific cross-linking by FXIIIa in fibrin structure and function
-
C. Duval, P. Allan, S.D. Connell, and et al. Roles of fibrin alpha- and gamma-chain specific cross-linking by FXIIIa in fibrin structure and function Thromb. Haemost. 111 5 2014 842 850
-
(2014)
Thromb. Haemost.
, vol.111
, Issue.5
, pp. 842-850
-
-
Duval, C.1
Allan, P.2
Connell, S.D.3
-
22
-
-
81755173567
-
Clot architecture is altered in abdominal aortic aneurysms and correlates with aneurysm size
-
D.J. Scott, P. Prasad, H. Philippou, and et al. Clot architecture is altered in abdominal aortic aneurysms and correlates with aneurysm size Arterioscler. Thromb. Vasc. Biol. 31 12 2011 3004 3010
-
(2011)
Arterioscler. Thromb. Vasc. Biol.
, vol.31
, Issue.12
, pp. 3004-3010
-
-
Scott, D.J.1
Prasad, P.2
Philippou, H.3
-
24
-
-
84912011601
-
Guideline for the diagnosis and management of the rare coagulation disorders: A United Kingdom Haemophilia Centre Doctors' Organization guideline on behalf of the British Committee for Standards in Haematology
-
A.D. Mumford, S. Ackroyd, R. Alikhan, and et al. Guideline for the diagnosis and management of the rare coagulation disorders: a United Kingdom Haemophilia Centre Doctors' Organization guideline on behalf of the British Committee for Standards in Haematology Br. J. Haematol. 167 3 2014 304 326
-
(2014)
Br. J. Haematol.
, vol.167
, Issue.3
, pp. 304-326
-
-
Mumford, A.D.1
Ackroyd, S.2
Alikhan, R.3
-
25
-
-
84941568112
-
Two symptomatic cases of dysfibrinogenemia in China: One with gamma-chain Arg275Cys mutation and another without detectable mutation in fibrinogen genes
-
Q. Bin, F. Liang, D.Y. Ou, and et al. Two symptomatic cases of dysfibrinogenemia in China: one with gamma-chain Arg275Cys mutation and another without detectable mutation in fibrinogen genes Blood Coagul. Fibrinolysis 26 5 2015 564 571
-
(2015)
Blood Coagul. Fibrinolysis
, vol.26
, Issue.5
, pp. 564-571
-
-
Bin, Q.1
Liang, F.2
Ou, D.Y.3
-
26
-
-
0023021611
-
Three abnormal fibrinogen variants with the same amino acid substitution (gamma 275 Arg - - His): Fibrinogens Bergamo II, Essen and Perugia
-
P. Reber, M. Furlan, A. Henschen, and et al. Three abnormal fibrinogen variants with the same amino acid substitution (gamma 275 Arg - - His): fibrinogens Bergamo II, Essen and Perugia Thromb. Haemost. 56 3 1986 401 406
-
(1986)
Thromb. Haemost.
, vol.56
, Issue.3
, pp. 401-406
-
-
Reber, P.1
Furlan, M.2
Henschen, A.3
-
27
-
-
84872271544
-
Clinical phenotype, laboratory features and genotype of 35 patients with heritable dysfibrinogenaemia
-
S.E. Shapiro, E. Phillips, R.A. Manning, and et al. Clinical phenotype, laboratory features and genotype of 35 patients with heritable dysfibrinogenaemia Br. J. Haematol. 160 2 2013 220 227
-
(2013)
Br. J. Haematol.
, vol.160
, Issue.2
, pp. 220-227
-
-
Shapiro, S.E.1
Phillips, E.2
Manning, R.A.3
-
28
-
-
70449392424
-
Two cases of congenital dysfibrinogenemia associated with thrombosis - Fibrinogen Praha III and Fibrinogen Plzen
-
R. Kotlin, Z. Reicheltova, M. Maly, and et al. Two cases of congenital dysfibrinogenemia associated with thrombosis - Fibrinogen Praha III and Fibrinogen Plzen Thromb. Haemost. 102 3 2009 479 486
-
(2009)
Thromb. Haemost.
, vol.102
, Issue.3
, pp. 479-486
-
-
Kotlin, R.1
Reicheltova, Z.2
Maly, M.3
-
29
-
-
35649001488
-
Fibrinogen Novy Jicin and Praha II: Cases of hereditary Aalpha 16 Arg → Cys and Aalpha 16 Arg → His dysfibrinogenemia
-
R. Kotlin, M. Chytilova, J. Suttnar, and et al. Fibrinogen Novy Jicin and Praha II: cases of hereditary Aalpha 16 Arg → Cys and Aalpha 16 Arg → His dysfibrinogenemia Thromb. Res. 121 1 2007 75 84
-
(2007)
Thromb. Res.
, vol.121
, Issue.1
, pp. 75-84
-
-
Kotlin, R.1
Chytilova, M.2
Suttnar, J.3
-
30
-
-
0037464816
-
Fibrinogen Magdeburg I: A novel variant of human fibrinogen with an amino acid exchange in the fibrinopeptide A (Aalpha 9, Leu → Pro)
-
M. Meyer, G. Kutscher, J. Sturzebecher, and et al. Fibrinogen Magdeburg I: a novel variant of human fibrinogen with an amino acid exchange in the fibrinopeptide A (Aalpha 9, Leu → Pro) Thromb. Res. 109 2-3 2003 145 151
-
(2003)
Thromb. Res.
, vol.109
, Issue.2-3
, pp. 145-151
-
-
Meyer, M.1
Kutscher, G.2
Sturzebecher, J.3
-
31
-
-
12844278573
-
Reduced plasma fibrinolytic potential is a risk factor for venous thrombosis
-
T. Lisman, P.G. de Groot, J.C. Meijers, and et al. Reduced plasma fibrinolytic potential is a risk factor for venous thrombosis Blood 105 3 2005 1102 1105
-
(2005)
Blood
, vol.105
, Issue.3
, pp. 1102-1105
-
-
Lisman, T.1
De Groot, P.G.2
Meijers, J.C.3
-
32
-
-
84883306104
-
Clot lysis phenotype and response to recombinant factor VIIa in plasma of haemophilia A inhibitor patients
-
K. Bakhtiari, P.W. Kamphuisen, M.E. Mancuso, and et al. Clot lysis phenotype and response to recombinant factor VIIa in plasma of haemophilia A inhibitor patients Br. J. Haematol. 162 6 2013 827 835
-
(2013)
Br. J. Haematol.
, vol.162
, Issue.6
, pp. 827-835
-
-
Bakhtiari, K.1
Kamphuisen, P.W.2
Mancuso, M.E.3
-
33
-
-
84871154512
-
Prediction of recurrent venous thromboembolism by clot lysis time: A prospective cohort study
-
L. Traby, M. Kollars, L. Eischer, and et al. Prediction of recurrent venous thromboembolism by clot lysis time: a prospective cohort study PLoS One 7 12 2012 e51447
-
(2012)
PLoS One
, vol.7
, Issue.12
-
-
Traby, L.1
Kollars, M.2
Eischer, L.3
-
34
-
-
84897485898
-
Prolonged duration of type 2 diabetes is associated with increased thrombin generation, prothrombotic fibrin clot phenotype and impaired fibrinolysis
-
M. Konieczynska, K. Fil, M. Bazanek, and et al. Prolonged duration of type 2 diabetes is associated with increased thrombin generation, prothrombotic fibrin clot phenotype and impaired fibrinolysis Thromb. Haemost. 111 4 2014 685 693
-
(2014)
Thromb. Haemost.
, vol.111
, Issue.4
, pp. 685-693
-
-
Konieczynska, M.1
Fil, K.2
Bazanek, M.3
-
35
-
-
84900811986
-
Altered plasma fibrin clot properties and fibrinolysis in patients with multiple myeloma
-
A. Undas, L. Zubkiewicz-Usnarska, G. Helbig, and et al. Altered plasma fibrin clot properties and fibrinolysis in patients with multiple myeloma Eur. J. Clin. Investig. 44 6 2014 557 566
-
(2014)
Eur. J. Clin. Investig.
, vol.44
, Issue.6
, pp. 557-566
-
-
Undas, A.1
Zubkiewicz-Usnarska, L.2
Helbig, G.3
-
36
-
-
84888419503
-
Partial deletion of the alphaC-domain in the Fibrinogen Perth variant is associated with thrombosis, increased clot strength and delayed fibrinolysis
-
S.K. Westbury, C. Duval, H. Philippou, and et al. Partial deletion of the alphaC-domain in the Fibrinogen Perth variant is associated with thrombosis, increased clot strength and delayed fibrinolysis Thromb. Haemost. 110 6 2013 1135 1144
-
(2013)
Thromb. Haemost.
, vol.110
, Issue.6
, pp. 1135-1144
-
-
Westbury, S.K.1
Duval, C.2
Philippou, H.3
-
37
-
-
0030068432
-
Fibrinogen Dusart: Electron microscopy of molecules, fibers and clots, and viscoelastic properties of clots
-
J.P. Collet, J.L. Woodhead, J. Soria, and et al. Fibrinogen Dusart: electron microscopy of molecules, fibers and clots, and viscoelastic properties of clots Biophys. J. 70 1 1996 500 510
-
(1996)
Biophys. J.
, vol.70
, Issue.1
, pp. 500-510
-
-
Collet, J.P.1
Woodhead, J.L.2
Soria, J.3
-
38
-
-
0029885335
-
The relationship between the fibrinogen D domain self-association/cross-linking site (gammaXL) and the fibrinogen Dusart abnormality (Aalpha R554C-albumin): Clues to thrombophilia in the "dusart syndrome"
-
M.W. Mosesson, K.R. Siebenlist, J. Hainfeld, and et al. The relationship between the fibrinogen D domain self-association/cross-linking site (gammaXL) and the fibrinogen Dusart abnormality (Aalpha R554C-albumin): clues to thrombophilia in the "Dusart syndrome" J. Clin. Invest. 97 10 1996 2342 2350
-
(1996)
J. Clin. Invest.
, vol.97
, Issue.10
, pp. 2342-2350
-
-
Mosesson, M.W.1
Siebenlist, K.R.2
Hainfeld, J.3
-
39
-
-
0242348804
-
Genetic regulation of fibrin structure and function: Complex gene-environment interactions may modulate vascular risk
-
B.C. Lim, R.A. Ariens, A.M. Carter, and et al. Genetic regulation of fibrin structure and function: complex gene-environment interactions may modulate vascular risk Lancet 361 9367 2003 1424 1431
-
(2003)
Lancet
, vol.361
, Issue.9367
, pp. 1424-1431
-
-
Lim, B.C.1
Ariens, R.A.2
Carter, A.M.3
-
40
-
-
0034554788
-
End-linked homodimers in fibrinogen Osaka VI with a B beta-chain extension lead to fragile clot structure
-
T. Sugo, C. Nakamikawa, N. Yoshida, and et al. End-linked homodimers in fibrinogen Osaka VI with a B beta-chain extension lead to fragile clot structure Blood 96 12 2000 3779 3785
-
(2000)
Blood
, vol.96
, Issue.12
, pp. 3779-3785
-
-
Sugo, T.1
Nakamikawa, C.2
Yoshida, N.3
-
41
-
-
80052315302
-
Two different fibrinogen gene mutations associated with bleeding in the same family (A alphaGly13Glu and gammaGly16Ser) and their impact on fibrin clot properties: Fibrinogen Krakow II and Krakow III
-
D. Pietrys, W. Balwierz, T. Iwaniec, and et al. Two different fibrinogen gene mutations associated with bleeding in the same family (A alphaGly13Glu and gammaGly16Ser) and their impact on fibrin clot properties: fibrinogen Krakow II and Krakow III Thromb. Haemost. 106 3 2011 558 560
-
(2011)
Thromb. Haemost.
, vol.106
, Issue.3
, pp. 558-560
-
-
Pietrys, D.1
Balwierz, W.2
Iwaniec, T.3
-
42
-
-
81755161511
-
Fibrin clot structure and function: A role in the pathophysiology of arterial and venous thromboembolic diseases
-
A. Undas, and R.A. Ariens Fibrin clot structure and function: a role in the pathophysiology of arterial and venous thromboembolic diseases Arterioscler. Thromb. Vasc. Biol. 31 12 2011 e88 e99
-
(2011)
Arterioscler. Thromb. Vasc. Biol.
, vol.31
, Issue.12
, pp. e88-e99
-
-
Undas, A.1
Ariens, R.A.2
|