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Bernard Soulier syndrome in pregnancy: a systematic review

Haemophilia : the official journal of the World Federation of Hemophilia, 2010-07, Vol.16 (4), p.584-591

2010

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High prevalence of elevated factor VIII levels in patients referred for thrombophilia screening: role of increased synthesis and relationship to the acute phase reaction

Thrombosis and haemostasis, 1997, Vol.77 (5), p.825-828

1997

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Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex

Nature genetics, 2003-06, Vol.34 (2), p.220-225

2003

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Definition of the bleeding tendency in factor XI-deficient kindreds--a clinical and laboratory study

Thrombosis and haemostasis, 1995, Vol.73 (2), p.194-202

1995

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Consensus protocol for the use of recombinant activated factor VII [eptacog alfa (activated); NovoSeven®] in elective orthopaedic surgery in haemophilic patients with inhibitors

Haemophilia : the official journal of the World Federation of Hemophilia, 2009-03, Vol.15 (2), p.501-508

2009

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Factor VII and cardiovascular risk

Thrombosis and haemostasis, 2005-02, Vol.93 (2), p.189-189

Tuddenham, E G D

2005

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Haemophilia A: mutation type determines risk of inhibitor formation

Thrombosis and haemostasis, 1995-12, Vol.74 (6), p.1402-1406

1995

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HLA genotype of patients with severe haemophilia A due to intron 22 inversion with and without inhibitors of factor VIII

Thrombosis and haemostasis, 1997-02, Vol.77 (2), p.238-242

1997

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Surface plasmon resonance studies of the interaction between factor VII and tissue factor. Demonstration of defective tissue factor binding in a variant FVII molecule (FVII-R79Q)

Biochemistry (Easton), 1994-11, Vol.33 (47), p.14162-14169

1994

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Prospects for gene therapy of haemophilia

Haemophilia : the official journal of the World Federation of Hemophilia, 2004-07, Vol.10 (4), p.309-318

2004

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Factor Xa and thrombin, but not factor VIIa, elicit specific cellular responses in dermal fibroblasts

Journal of thrombosis and haemostasis, 2003-09, Vol.1 (9), p.1935-1944

2003

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Crystal structure of the extracellular region of human tissue factor

Nature (London), 1994-08, Vol.370 (6491), p.662-666

1994

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Postinjury vascular intimal hyperplasia in mice is completely inhibited by CD34+ bone marrow‐derived progenitor cells expressing membrane‐tethered anticoagulant fusion proteins

Journal of thrombosis and haemostasis, 2006-10, Vol.4 (10), p.2191-2198

2006

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Bleeding symptoms in 27 Iranian patients with the combined deficiency of factor V and factor VIII

British journal of haematology, 1998-03, Vol.100 (4), p.773-776

1998

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Factor V I359T: a novel mutation associated with thrombosis and resistance to activated protein C

British journal of haematology, 2003-11, Vol.123 (3), p.496-501

2003

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In search of the eighth factor: a personal reminiscence

Journal of thrombosis and haemostasis, 2003-03, Vol.1 (3), p.403-409

Tuddenham, E. G. D.

2003

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Classification of rare bleeding disorders (RBDs) based on the association between coagulant factor activity and clinical bleeding severity

Journal of thrombosis and haemostasis, 2012-09, Vol.10 (9), p.1938-1943

2012

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Analysis of the consequences of premature termination codons within factor VIII coding sequences

Journal of thrombosis and haemostasis, 2003-01, Vol.1 (1), p.139-146

2003

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BIOPSY OF HUMAN PREIMPLANTATION EMBRYOS AND SEXING BY DNA AMPLIFICATION

The Lancet (British edition), 1989-02, Vol.333 (8634), p.347-349

1989

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Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381 → Ser) in the substrate‐binding pocket

British journal of haematology, 1993-06, Vol.84 (2), p.285-289

1993

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A molecular model for the triplicated A domains of human factor VIII based on the crystal structure of human ceruloplasmin

Blood, 1997-04, Vol.89 (7), p.2413-2421

1997

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Relationships of plasma viscosity, coagulation and fibrinolysis to coronary risk factors and angina

Thrombosis and haemostasis, 1991-04, Vol.65 (4), p.339-343

1991

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Analysis of the essential sequences of the factor VIII gene in twelve haemophilia A patients by single-stranded conformation polymorphism

Blood coagulation & fibrinolysis, 1994-04, Vol.5 (2), p.257-264

1994

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Factor VIII gene mutations found by a comparative study of SSCP, DGGE and CMC and their analysis on a molecular model of factor VIII protein

Human genetics, 1997-12, Vol.101 (3), p.323-332

1997

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Molecular defects in CRM+ factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVII

British journal of haematology, 1994-03, Vol.86 (3), p.610-618

1994

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Bernard Soulier syndrome in pregnancy: a systematic review

High prevalence of elevated factor VIII levels in patients referred for thrombophilia screening: role of increased synthesis and relationship to the acute phase reaction

Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex

Definition of the bleeding tendency in factor XI-deficient kindreds--a clinical and laboratory study

Consensus protocol for the use of recombinant activated factor VII [eptacog alfa (activated); NovoSeven®] in elective orthopaedic surgery in haemophilic patients with inhibitors

Factor VII and cardiovascular risk

Haemophilia A: mutation type determines risk of inhibitor formation

HLA genotype of patients with severe haemophilia A due to intron 22 inversion with and without inhibitors of factor VIII

Surface plasmon resonance studies of the interaction between factor VII and tissue factor. Demonstration of defective tissue factor binding in a variant FVII molecule (FVII-R79Q)

Prospects for gene therapy of haemophilia

Factor Xa and thrombin, but not factor VIIa, elicit specific cellular responses in dermal fibroblasts

Crystal structure of the extracellular region of human tissue factor

Postinjury vascular intimal hyperplasia in mice is completely inhibited by CD34+ bone marrow‐derived progenitor cells expressing membrane‐tethered anticoagulant fusion proteins

Bleeding symptoms in 27 Iranian patients with the combined deficiency of factor V and factor VIII

Factor V I359T: a novel mutation associated with thrombosis and resistance to activated protein C

In search of the eighth factor: a personal reminiscence

Classification of rare bleeding disorders (RBDs) based on the association between coagulant factor activity and clinical bleeding severity

Analysis of the consequences of premature termination codons within factor VIII coding sequences

BIOPSY OF HUMAN PREIMPLANTATION EMBRYOS AND SEXING BY DNA AMPLIFICATION

Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381 → Ser) in the substrate‐binding pocket

A molecular model for the triplicated A domains of human factor VIII based on the crystal structure of human ceruloplasmin

Relationships of plasma viscosity, coagulation and fibrinolysis to coronary risk factors and angina

Analysis of the essential sequences of the factor VIII gene in twelve haemophilia A patients by single-stranded conformation polymorphism

Factor VIII gene mutations found by a comparative study of SSCP, DGGE and CMC and their analysis on a molecular model of factor VIII protein

Molecular defects in CRM+ factor VII deficiencies: modelling of missense mutations in the catalytic domain of FVII

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