Zobrazeno 1 - 10
of 296
pro vyhledávání: '"J. F. Schved"'
Autor:
A. Theron, S. Ayadi, E. Boissier, O. Dautremay, J.-F. Schved, N. Sirvent, I. Diaz, G. Captier, C. Biron-Andreani, E. Jeziorski
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
IntroductionIdiopathic purpura fulminans (IPF) is a rare and severe coagulation disorder, associated with transient anti-protein S (anti-PS) antibodies in the context of post-viral infection such as varicella. Anti-protein S antibodies are frequently
Externí odkaz:
https://doaj.org/article/cbb0945dbbd645088b693c2364a9a8e3
Autor:
U Nowak-Göttl, C Hermans, J Mahlangu, S Ahuja, M Carcao, G Castaman, J Davis, O Khan, W Miesbach, M Reding, J-F Schved, L Villareal Martinez, M Wang, J Windyga, M Witkop, G Young, D Bonzo, I Mitchell, C Kessler
Publikováno v:
GTH Congress 2023 – 67th Annual Meeting of the Society of Thrombosis and Haemostasis Research – The patient as a benchmark.
Autor:
Guy Young, Doris Quon, Janna M. Journeycake, Ismail Haroon Mitha, Thomas A. Wilkinson, Ahmad Al-Sabbagh, Johnny Mahlangu, Alok Srivastava, Philippe de Moerloose, Giancarlo Castaman, Craig M. Kessler, Kateryna V. Vilchevska, Michael Recht, Cédric Hermans, W. Allan Alexander, Michael U. Callaghan, J.-F. Schved, Santiago Bonanad Boix, James V. Luck, Oleksandra Stasyshyn, Wolfgang Miesbach, Robert F. Sidonio, Michael Wang, Amy D. Shapiro, Miguel A. Escobar, Claude Negrier, Jonathan M. Ducore, Christopher Macie, Daniel Bonzo, Cindy A. Leissinger
Publikováno v:
HAEMOPHILIA
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Haemophilia, Vol. 27, no. 6, p. 921-931 (2021)
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Haemophilia, Vol. 27, no. 6, p. 921-931 (2021)
Introduction Haemophilia patients with inhibitors often require a bypassing agent (BPA) for bleeding episode management. Eptacog beta (EB) is a new FDA-approved recombinant activated human factor VII BPA for the treatment and control of bleeding in h
Autor:
Jerzy Windyga, Ian S Mitchell, Yevhenii Averianov, Adam Giermasz, Maria Fernanda Lopez Fernandez, Laura Villarreal Martinez, W. Allan Alexander, Wolfgang Miesbach, Oleksandra Stasyshyn, Ismail Haroon Mitha, Daniel P. Hart, James V. Luck, Janna M. Journeycake, Miguel A. Escobar, Daniel Bonzo, Cindy A. Leissinger, Cédric Hermans, Mark T. Reding, J.-F. Schved, Kateryna V. Vilchevska, Craig M. Kessler, Jonathan M. Ducore, Doris Quon, Thomas A. Wilkinson, Johnny Mahlangu, Ahmad Al-Sabbagh, Michael Wang
Publikováno v:
Haemophilia, Vol. 27, no. 6, p. 911-920 (2021)
Introduction Surgical procedures in persons with haemophilia A or B with inhibitors (PwHABI) require the use of bypassing agents (BPA) and carry a high risk of complications. Historically, only two BPAs have been available; these are reported to have
Akademický článek
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Autor:
J.-F. Schved, J.-P. Laroche
Publikováno v:
Journal des Maladies Vasculaires. 41:383-388
Vitamin K antagonists (VKA) and direct oral anticoagulants (DOACs) are now in competition. The companies are trying to replace VKA by DOACs, totally or at least greatly VKA should VKA disappear in favor of DOACs? There are still many questions about
Akademický článek
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Autor:
Alberto Tosetto, Elena Santagostino, Mt. Álvarez-Román, U. Scholz, Stefan Lethagen, Giancarlo Castaman, Christopher A. Ludlam, C. R. M. Hay, Johannes Oldenburg, Gerry Dolan, R. Parra Lopez, Marc Trossaert, Cédric Hermans, Margareta Holmström, Silvia Linari, J.-F. Schved, T. Albert, A. Boban, Erik Berntorp
Publikováno v:
Haemophilia. 23:105-114
Introduction: Haemophilia treatment varies significantly between individuals, countries and regions and details of bleed rates, factor consumption and injection frequency are often not available. Aim: To provide an overview of the FVIII/FIX treatment
Publikováno v:
Journal de medecine vasculaire. 43(3)
In 2008, we decided to enter the era of direct oral anticoagulants (DOACS). Was that the right decision to make? The answer will depend on how well we meet the conditions of proper use. This means avoiding underdosing and overdosing as well as unders
Autor:
J.-F. Schved
Publikováno v:
Transfusion Clinique et Biologique. 22:85-89
Until 1990, congenital hemorrhagic disorders were treated by plasma-derived concentrates. The first recombinant drug, recombinant factor VIII was available after this date and few years later recombinant factor IX could also be proposed to patients.