Kolexia
De Mazancourt Philippe Biologie médicale
De Mazancourt Philippe
Biologie médicale
Hôpital Ambroise Paré
Boulogne-Billancourt, France
75 Activités
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Scientifique
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Sujets de recherche
{{person.topmesh1.name}} Afibrinogénémie Déficit en facteur XI Hémorragie Syndrome d'Ehlers-Danlos Tumeurs de l'utérus Thrombose Complications de la grossesse Choriocarcinome Maladie de Fabry

Collaborateurs

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Vialard Francois
Vialard Francois
Chi Poissy St Germain Site De Poissy, Poissy, France
Serazin-Leroy Valerie
Serazin-Leroy Valerie
Chi Poissy St Germain Site De Poissy, Poissy, France
Hanss Michel
Hanss Michel
Hôpital Pierre Wertheimer, Bron, France
Wainer Robert
Wainer Robert
Chi Poissy St Germain Site De Poissy, Poissy, France

Industries

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Pfizer
1 collaboration(s)
Dernière en 2017
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Dernières activités

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Absence of Missense Variant Detection in Inherited Dysfibrinogenemia May Result from a Poor Raw Data Analysis Algorithm or Mosaicism.
International journal of molecular sciences   21 novembre 2023
A focus on dominant negative variants in a series of 170 heterozygous FXI-deficient patients.
Haemophilia : the official journal of the World Federation of Hemophilia   30 mai 2023
A severe case of -related kyphoscoliotic Ehlers-Danlos syndrome associated with several arterial and venous complications: A case report.
Clinical case reports   27 février 2023
Management of rare inherited bleeding disorders: Proposals of the French Reference Centre on Haemophilia and Rare Coagulation Disorders.
European journal of haematology   20 février 2023
Classical Ehlers-Danlos syndrome with severe kyphoscoliosis due to a novel pathogenic variant of .
Clinical case reports   28 novembre 2022
110.1 Prophylaxis with human coagulation factor X in an adolescent girl with hereditary major Stuart factor deficiency
Abstracts of the ISTH 2022 Congress of the International Society of Thrombosis and Haemostasis, July 9–13, 2022   21 octobre 2022
116.1 Usefulness of rotational plasma thromboelastometry in severe inherited FXIII deficiency
Abstracts of the ISTH 2022 Congress of the International Society of Thrombosis and Haemostasis, July 9–13, 2022   21 octobre 2022
Reinvestigation of unidentified causative variants in FXI-deficient patients: Focus on gene segment deletions.
Haemophilia : the official journal of the World Federation of Hemophilia   04 octobre 2022
Clinical, biological, and genetic features in an afibrinogenemia patient series in Algeria.
Haemophilia : the official journal of the World Federation of Hemophilia   30 avril 2022
PO167 ACCIDENTAL DISCOVERY OF AN UNUSUAL CONSTITUTIONAL DYSFIBRINOGENEMIA: LONGMONT FIBRINOGEN
15th Annual Congress of European Association for Haemophilia and Allied Disorders 2022, 2–4 February 2022, Virtual Meeting   31 janvier 2022