Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Sandrine Meunier"'
Autor:
Koyo Usuba, Victoria E. Price, Victor Blanchette, Audrey Abad, Carmen Altisent, Loretta Buchner‐Daley, Jorge D. A. Carneiro, Brian M. Feldman, Kathelijn Fischer, John Grainger, Susanne Holzhauer, Koon‐Hung Luke, Sandrine Meunier, Margareth Ozelo, Ling Tang, Sandra V. Antunes, Paula Villaça, Cindy Wakefield, Gilian Wharfe, Runhui Wu, Nancy L. Young
Publikováno v:
Research and Practice in Thrombosis and Haemostasis, Vol 3, Iss 3, Pp 397-404 (2019)
Background Prophylaxis reduces the frequency of bleeds in boys with severe hemophilia and is the standard care for their management in resource‐abundant countries. The effect of prophylaxis on Health‐Related Quality of Life (HRQoL) has not been e
Externí odkaz:
https://doaj.org/article/c5077a944a5343218ad80df8127c8ccd
Autor:
Mathilde Penel-Page, Sandrine Meunier, Mathilde Fretigny, Sandra Le Quellec, Pierre Boisseau, Christine Vinciguerra, Catherine Ternisien, Lucia Rugeri
Publikováno v:
Platelets, Vol 28, Iss 8, Pp 825-828 (2017)
At birth, severe thrombocytopenia without context of infection should mainly suggest neonatal alloimmune thrombocytopenia (NAIT), especially in case of a platelet count below 20 GL−1. We report two cases of severe neonatal thrombocytopenia, first s
Externí odkaz:
https://doaj.org/article/405549e039d84c479a582c1853221878
Autor:
Stéphanie Désage, Yesim Dargaud, Sandrine Meunier, Sandra Le Quellec, Anne Lienhart, Claude Negrier, Christophe Nougier, Lucia Rugeri
Publikováno v:
Haemophilia. 28:301-307
In patients with FXI deficiency, the risk of surgery-related bleeding is poorly correlated with plasma FXI activity (FXI:C); the latter can therefore not be used as a reliable predictor of bleeding in surgeries.The aim of this retrospective study was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5aae087a9afab8a9cb0b04bed58827e9
https://doi.org/10.1111/hae.14506
https://doi.org/10.1111/hae.14506
Autor:
Tania Attié-Bitach, Alix Mathonnet, Sandrine Meunier, Charline Cartellier, Renaud Touraine, Marianne Till, Audrey Putoux, Séverine Cunat, Sandrine Caillot, Cyrielle Thonnon, Massimiliano Rossi, Jocelyne Attia, Fabienne Allias
Publikováno v:
American Journal of Medical Genetics Part A. 188:314-318
Congenital combined vitamin K-dependent clotting factors deficiency (VKCFD) is a rare autosomal recessive disease resulting in hemorrhagic symptoms usually associated with developmental disorders and bone abnormalities. Pathogenic variants in two gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1015798ad5ddd46d0918c4f41048de57
https://doi.org/10.1002/ajmg.a.62503
https://doi.org/10.1002/ajmg.a.62503
Autor:
Nathalie Grinda, Francoise Truong-Berthoz, Edita Dolimier, Emmanuelle Ferré, Birgit Frotscher, Emmanuelle de Raucourt, Valerie Roussel-Robert, Sophie Bayart, Sandrine Meunier, Sophie le Doré, Pierre Chamouni
Publikováno v:
Journal of Blood Medicine
Sophie le Doré,1 Nathalie Grinda,2 Emmanuelle Ferré,1 Valerie Roussel-Robert,3 Birgit Frotscher,4 Pierre Chamouni,5 Sandrine Meunier,6 Sophie Bayart,7 Edita Dolimier,8 Francoise Truong-Berthoz,9 Emmanuelle de Raucourt1 1Haemophilia Treatment Centre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d595a040a8497e3fcb1eb64f9a53a93a
https://doi.org/10.2147/jbm.s280032
https://doi.org/10.2147/jbm.s280032
Publikováno v:
Therapies. 76:23-29
Prophylaxis treatment is considered as the reference approach for children with severe haemophilia A or B. However, no consensus about the best prophylaxis protocol has yet been identified in term of dosage and timing of infusions. Guidelines were dr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d38674b662dbf64c1072c0677b9e3b5e
https://doi.org/10.1016/j.therap.2020.06.014
https://doi.org/10.1016/j.therap.2020.06.014
Autor:
Sandrine MEUNIER
Publikováno v:
EMC - Pediatría. 55:1-9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4b652507b1e626bc9612180e77f7346
https://doi.org/10.1016/s1245-1789(20)44338-0
https://doi.org/10.1016/s1245-1789(20)44338-0
Autor:
Lucia Rugeri, Annie Harroche, Yohan Repessé, Dominique Desprez, Brigitte Pan Petesch, Pierre Chamouni, Christine Biron, Birgit Frotscher, Hasan Catovic, Diane Bracquart, Cédric Martin, Marc Trossaërt, Sandrine Meunier, Roseline d'Oiron
Publikováno v:
European journal of haematology. 109(1)
Patients with symptomatic von Willebrand disease (VWD) should be offered long-term prophylaxis (LTP) to prevent recurrent bleedings. Our objective was to evaluate the effectiveness and safety of Voncento®, a plasma-derived FVIII/VWF concentrate (rat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbd341b67ed0b1cf31da1626eb54a5b6
https://pubmed.ncbi.nlm.nih.gov/35438801
https://pubmed.ncbi.nlm.nih.gov/35438801
Publikováno v:
Hématologie. 26:192-200
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::817123be03e4d9f2c9ee79b34472897c
https://doi.org/10.1684/hma.2020.1571
https://doi.org/10.1684/hma.2020.1571
Autor:
Anemoon Torfs, Laurent Chardonnal, Sandrine Meunier, Stéphanie Désage, Roland Henaine, Marc Lilot
Publikováno v:
Journal of cardiothoracic and vascular anesthesia. 36(10)
Hemophilia A is an inherited bleeding disorder characterized by a lack of plasma clotting factor VIII (FVIII). In prophylaxis or during surgery, FVIII infusions are necessary to prevent bleeding. The authors describe the perioperative challenges and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6df5b672a850c7ad3e9252eed2704384
https://pubmed.ncbi.nlm.nih.gov/35879147
https://pubmed.ncbi.nlm.nih.gov/35879147