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Rare coagulation disorders: fibrinogen, factor VII and factor XIII

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-07, Vol.22 (S5), p.61-65

2016

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European retrospective study of real‐life haemophilia treatment

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-01, Vol.23 (1), p.105-114

2017

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A retrospective analysis of 157 surgical procedures performed without replacement therapy in 83 unrelated factor VII‐deficient patients

Journal of thrombosis and haemostasis, 2011-06, Vol.9 (6), p.1149-1156

2011

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PERSEPT 1: a phase 3 trial of activated eptacog beta for on‐demand treatment of haemophilia inhibitor‐related bleeding

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-11, Vol.23 (6), p.832-843

2017

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Women with congenital factor VII deficiency: clinical phenotype and treatment options from two international studies

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-09, Vol.22 (5), p.752-759

2016

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After the SIPPET study: Position paper of the CoMETH, the French society of haemophilia

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-03, Vol.24 (2), p.e55-e57

2018

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Relationship between paraoxonase‐1 activity, its Q192R genetic variant and clopidogrel responsiveness in the ADRIE study

Journal of thrombosis and haemostasis, 2011-08, Vol.9 (8), p.1664-1666

2011

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Post-viral idiopathic purpura fulminans is associated with inherited thrombophilia and anti-cardiolipin antibodies

Frontiers in pediatrics, 2023-05, Vol.11, p.1197795-1197795

2023

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Chemical vs. radioactive synoviorthesis for treatment of chronic haemophilic synovitis: Syrian experience

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-11, Vol.22 (6), p.e573-e575

2016

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Computer-predicted peptides that mimic discontinuous epitopes on the A2 domain of factor VIII

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-05, Vol.21 (3), p.e193-e201

2015

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Influence of surgical bleeding on the relationship between admission coagulopathy and risk of massive transfusion: lesson from 704 severe trauma patients

Vox sanguinis, 2016-08, Vol.111 (2), p.151-160

2016

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Clinical predictors of dual aspirin and clopidogrel poor responsiveness in stable cardiovascular patients from the ADRIE study

Journal of thrombosis and haemostasis, 2010-12, Vol.8 (12), p.2614-2623

2010

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Cancer detection and management in patients with haemophilia: a retrospective European multicentre study

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-01, Vol.20 (1), p.78-82

2014

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Genotype and phenotype relationships in 10 Pakistani unrelated patients with inherited factor VII deficiency

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-11, Vol.19 (6), p.893-897

2013

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Are low-density lipoprotein receptor-related protein 1 or non-neutralizing antibodies predictors of FVIII in vivo recovery in haemophilia A patients?

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-11, Vol.20 (6), p.e406-e408

2014

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The paradoxical association between inherited factor VII deficiency and venous thrombosis

Haemophilia : the official journal of the World Federation of Hemophilia, 2008-05, Vol.14 (3), p.564-570

2008

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Thrombosis in inherited factor VII deficiency

Journal of thrombosis and haemostasis, 2003-10, Vol.1 (10), p.2153-2158

2003

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A Haut-Doubs FVII variant depending on species-derived-thromboplastin reagent (F7:p.Arg337His)

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-07, Vol.20 (4), p.e347-e349

2014

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Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders

Journal of thrombosis and haemostasis, 2012-04, Vol.10 (4), p.615-621

2012

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A multi‐stage multi‐design strategy provides strong evidence that the BAI3 locus is associated with early‐onset venous thromboembolism

Journal of thrombosis and haemostasis, 2010-12, Vol.8 (12), p.2671-2679

2010

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Circulating FVIII-specific IgG, IgA and IgM memory B cells from haemophilia A patients

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-09, Vol.22 (5), p.799-805

2016

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Prophylaxis in congenital factor VII deficiency: indications, efficacy and safety. Results from the Seven Treatment Evaluation Registry (STER)

Haematologica (Roma), 2013-04, Vol.98 (4), p.538-544

2013

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Variable phenotypic presentation of iron overload in H63D homozygotes: are genetic modifiers the cause?

Gut, 2001-06, Vol.48 (6), p.836-842

2001

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Characterizing hospital pathways for the care of acquired hemophilia in France using comprehensive national health data

La revue de medecine interne, 2022-03, Vol.43 (3), p.139-144

2022

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Maladies hémorragiques congénitales : quel avenir pour les dérivés plasmatiques par rapport aux recombinants et aux produits sanguins labiles ?

Transfusion clinique et biologique : journal de la Société française de transfusion sanguine, 2015-08, Vol.22 (3), p.85-89

Schved, J.-F.

2015

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Rare coagulation disorders: fibrinogen, factor VII and factor XIII

European retrospective study of real‐life haemophilia treatment

A retrospective analysis of 157 surgical procedures performed without replacement therapy in 83 unrelated factor VII‐deficient patients

PERSEPT 1: a phase 3 trial of activated eptacog beta for on‐demand treatment of haemophilia inhibitor‐related bleeding

Women with congenital factor VII deficiency: clinical phenotype and treatment options from two international studies

After the SIPPET study: Position paper of the CoMETH, the French society of haemophilia

Relationship between paraoxonase‐1 activity, its Q192R genetic variant and clopidogrel responsiveness in the ADRIE study

Post-viral idiopathic purpura fulminans is associated with inherited thrombophilia and anti-cardiolipin antibodies

Chemical vs. radioactive synoviorthesis for treatment of chronic haemophilic synovitis: Syrian experience

Computer-predicted peptides that mimic discontinuous epitopes on the A2 domain of factor VIII

Influence of surgical bleeding on the relationship between admission coagulopathy and risk of massive transfusion: lesson from 704 severe trauma patients

Clinical predictors of dual aspirin and clopidogrel poor responsiveness in stable cardiovascular patients from the ADRIE study

Cancer detection and management in patients with haemophilia: a retrospective European multicentre study

Genotype and phenotype relationships in 10 Pakistani unrelated patients with inherited factor VII deficiency

Are low-density lipoprotein receptor-related protein 1 or non-neutralizing antibodies predictors of FVIII in vivo recovery in haemophilia A patients?

The paradoxical association between inherited factor VII deficiency and venous thrombosis

Thrombosis in inherited factor VII deficiency

A Haut-Doubs FVII variant depending on species-derived-thromboplastin reagent (F7:p.Arg337His)

Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders

A multi‐stage multi‐design strategy provides strong evidence that the BAI3 locus is associated with early‐onset venous thromboembolism

Circulating FVIII-specific IgG, IgA and IgM memory B cells from haemophilia A patients

Prophylaxis in congenital factor VII deficiency: indications, efficacy and safety. Results from the Seven Treatment Evaluation Registry (STER)

Variable phenotypic presentation of iron overload in H63D homozygotes: are genetic modifiers the cause?

Characterizing hospital pathways for the care of acquired hemophilia in France using comprehensive national health data

Maladies hémorragiques congénitales : quel avenir pour les dérivés plasmatiques par rapport aux recombinants et aux produits sanguins labiles ?

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