UB Paderborn / Katalog / Suche / in CDI

Obesity and risk of venous thromboembolism among postmenopausal women: differential impact of hormone therapy by route of estrogen administration. The ESTHER Study

Journal of thrombosis and haemostasis, 2006-06, Vol.4 (6), p.1259-1265

2006

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Post-operative use of heparin increases morbidity of pacemaker implantation

Europace (London, England), 2006-04, Vol.8 (4), p.283-287

2006

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W365 PREECLAMPSIA AS A RISK FACTOR FOR POSTNATAL PULMONARY EMBOLISM

International journal of gynecology and obstetrics, 2012-10, Vol.119 (S3), p.S823-S823

2012

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Thrombose et contraception estroprogestative : mise au point du groupe de travail pluridisciplinaire CNGOF-FNCGM-GEHT-SFMV

Journal de gynécologie, obstétrique et biologie de la reproduction, 2013-06, Vol.42 (4), p.309-315

2013

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P.4 Preeclampsia as a risk factor for postnatal pulmonary embolism

Thrombosis research, 2011, Vol.127, p.S130-S130

2011

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Le variant thermolabile de la méthylènetétrahydrofolate réductase (MTHFR) est-il un facteur de risque de thrombotique artériel et veineux ?

La revue de medecine interne, 1997, Vol.18, p.657s-659s

1997

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Hormone therapy and venous thromboembolism among postmenopausal women : Impact of the route of estrogen administration and progestogens: The ESTHER study

Circulation (New York, N.Y.), 2007-02, Vol.115 (7), p.840-845

2007

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La thrombocytose au cours des traitements par héparine de bas poids moléculaire : une situation plus fréquente qu’on ne le croit ?

Journal des maladies vasculaires, 2010-12, Vol.35 (6), p.348-351

2010

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Prevalence of ovarian hyperstimulation syndrome (OHSS) and hypercoagulability in patients triggered by GnRH agonist for excessive follicular response: a systematic follow-up

Fertility and sterility, 2017-09, Vol.108 (3), p.e227-e227

2017

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Microparticle phenotypes are associated with driver mutations and distinct thrombotic risks in essential thrombocythemia

Haematologica (Roma), 2016-09, Vol.101 (9), p.e365

2016

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Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia

Haematologica (Roma), 2014-08, Vol.99 (8), p.1387

2014

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Thrombotic risk according to SERPINC1 genotype in a large cohort of subjects with antithrombin inherited deficiency

Thrombosis and haemostasis, 2017, Vol.117 (6), p.1040

2017

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PB1439 Diversity of Hereditary Protein C Deficiency in North France: A Genotype-Phenotype Correlation

Research and practice in thrombosis and haemostasis, 2023-10, Vol.7, p.101778, Article 101778

2023

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Traitement substitutif de la ménopause et risque thrombotique veineux

Gynécologie, obstétrique & fertilité, 2004-09, Vol.32 (9), p.725-728

2004

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Prothrombotic mutations, hormone therapy, and venous thromboembolism among postmenopausal women : Impact of the route of estrogen administration

Circulation (New York, N.Y.), 2005-11, Vol.112 (22), p.3495-3500

2005

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Maladie de Vaquez : risques et prise en charge au cours de la grossesse

Gynécologie, obstétrique & fertilité, 2005-05, Vol.33 (5), p.331-337

2005

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FranceCoag: a 22-year prospective follow-up of the national French cohort of patients with inherited bleeding disorders

European journal of epidemiology, 2019-05, Vol.34 (5), p.521-532

2019

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OC 75.2 Obstetrical Complications in Hereditary Fibrinogen Disorders: The Fibrinogest Study

Research and practice in thrombosis and haemostasis, 2023-10, Vol.7, p.100477, Article 100477

2023

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Devant quelles manifestations vasculaires rechercher un syndrome myéloprolifératif ?

Journal des maladies vasculaires, 2000, Vol.25 (5), p.382-387

2000

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Homozygous G20210A transition in the prothrombin gene associated with severe venous thrombotic disease: two cases in a French family

Thrombosis and haemostasis, 1998-12, Vol.80 (6), p.1027

1998

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Prophylactic and therapeutic recombinant factor VIIa administration to patients with Glanzmann's thrombasthenia: results of an international survey

Journal of thrombosis and haemostasis, 2004-07, Vol.2 (7), p.1096-1103

2004

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Recommendations on Testing for Thrombophilia in Venous Thromboembolic Disease: a French Consensus Guideline

Journal des maladies vasculaires, 2009-05, Vol.34 (3), p.156-203

2009

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Le variant thermolabile de la méthylènetétrahydrofolate réductase (MTHFR) est-il un facteur de risque de thrombotique artériel et veineux ?: Actualités vasculaires sur la maladie thromboembolique

La revue de medecine interne, 1997, Vol.18, p.657s-659s

1997

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Protein S inherited qualitative deficiency: novel mutations and phenotypic influence

Journal of thrombosis and haemostasis, 2010-12, Vol.8 (12), p.2718-2726

2010

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Le réseau G4 thrombose de l’inter-région Nord-Ouest : mise en place et premiers travaux

Journal des maladies vasculaires, 2011-09, Vol.36 (5), p.326-326

2011

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Obesity and risk of venous thromboembolism among postmenopausal women: differential impact of hormone therapy by route of estrogen administration. The ESTHER Study

Post-operative use of heparin increases morbidity of pacemaker implantation

W365 PREECLAMPSIA AS A RISK FACTOR FOR POSTNATAL PULMONARY EMBOLISM

Thrombose et contraception estroprogestative : mise au point du groupe de travail pluridisciplinaire CNGOF-FNCGM-GEHT-SFMV

P.4 Preeclampsia as a risk factor for postnatal pulmonary embolism

Le variant thermolabile de la méthylènetétrahydrofolate réductase (MTHFR) est-il un facteur de risque de thrombotique artériel et veineux ?

Hormone therapy and venous thromboembolism among postmenopausal women : Impact of the route of estrogen administration and progestogens: The ESTHER study

La thrombocytose au cours des traitements par héparine de bas poids moléculaire : une situation plus fréquente qu’on ne le croit ?

Prevalence of ovarian hyperstimulation syndrome (OHSS) and hypercoagulability in patients triggered by GnRH agonist for excessive follicular response: a systematic follow-up

Microparticle phenotypes are associated with driver mutations and distinct thrombotic risks in essential thrombocythemia

Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia

Thrombotic risk according to SERPINC1 genotype in a large cohort of subjects with antithrombin inherited deficiency

PB1439 Diversity of Hereditary Protein C Deficiency in North France: A Genotype-Phenotype Correlation

Traitement substitutif de la ménopause et risque thrombotique veineux

Prothrombotic mutations, hormone therapy, and venous thromboembolism among postmenopausal women : Impact of the route of estrogen administration

Maladie de Vaquez : risques et prise en charge au cours de la grossesse

FranceCoag: a 22-year prospective follow-up of the national French cohort of patients with inherited bleeding disorders

OC 75.2 Obstetrical Complications in Hereditary Fibrinogen Disorders: The Fibrinogest Study

Devant quelles manifestations vasculaires rechercher un syndrome myéloprolifératif ?

Homozygous G20210A transition in the prothrombin gene associated with severe venous thrombotic disease: two cases in a French family

Prophylactic and therapeutic recombinant factor VIIa administration to patients with Glanzmann's thrombasthenia: results of an international survey

Recommendations on Testing for Thrombophilia in Venous Thromboembolic Disease: a French Consensus Guideline

Le variant thermolabile de la méthylènetétrahydrofolate réductase (MTHFR) est-il un facteur de risque de thrombotique artériel et veineux ?: Actualités vasculaires sur la maladie thromboembolique

Protein S inherited qualitative deficiency: novel mutations and phenotypic influence

Le réseau G4 thrombose de l’inter-région Nord-Ouest : mise en place et premiers travaux

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