Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Marie‐Françoise Hurtaud‐Roux"'
Autor:
Béatrice Saposnik, Sylvie Binard, Odile Fenneteau, Alan Nurden, Paquita Nurden, Marie‐Françoise Hurtaud‐Roux, Nicole Schlegel, the French MYH9 network
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 2, Iss 4, Pp 297-312 (2014)
Abstract MYH9‐Related Disorders are a group of rare autosomal dominant platelet disorders presenting as nonsyndromic forms characterized by macrothrombocytopenia with giant platelets and leukocyte inclusion bodies or as syndromic forms combining th
Externí odkaz:
https://doaj.org/article/f8b0267af6f94c31abf41c0135089159
Autor:
Patrizia Noris, Nicole Schlegel, Catherine Klersy, Paula G. Heller, Elisa Civaschi, Nuria Pujol-Moix, Fabrizio Fabris, Remi Favier, Paolo Gresele, Véronique Latger-Cannard, Adam Cuker, Paquita Nurden, Andreas Greinacher, Marco Cattaneo, Erica De Candia, Alessandro Pecci, Marie-Françoise Hurtaud-Roux, Ana C. Glembotsky, Eduardo Muñiz-Diaz, Maria Luigia Randi, Nathalie Trillot, Loredana Bury, Thomas Lecompte, Caterina Marconi, Anna Savoia, Carlo L. Balduini, Sophie Bayart, Anne Bauters, Schéhérazade Benabdallah-Guedira, Françoise Boehlen, Jeanne-Yvonne Borg, Roberta Bottega, James Bussel, Daniela De Rocco, Emmanuel de Maistre, Michela Faleschini, Emanuela Falcinelli, Silvia Ferrari, Alina Ferster, Tiziana Fierro, Dominique Fleury, Pierre Fontana, Chloé James, Francois Lanza, Véronique Le Cam Duchez, Giuseppe Loffredo, Pamela Magini, Dominique Martin-Coignard, Fanny Menard, Sandra Mercier, Annamaria Mezzasoma, Pietro Minuz, Ilaria Nichele, Lucia D. Notarangelo, Tommaso Pippucci, Gian Marco Podda, Catherine Pouymayou, Agnes Rigouzzo, Bruno Royer, Pierre Sie, Virginie Siguret, Catherine Trichet, Alessandra Tucci, Béatrice Saposnik, Dino Veneri
Publikováno v:
Haematologica, Vol 99, Iss 8 (2014)
Pregnancy in women with inherited thrombocytopenias is a major matter of concern as both the mothers and the newborns are potentially at risk of bleeding. However, medical management of this condition cannot be based on evidence because of the lack o
Externí odkaz:
https://doaj.org/article/7a05c6d478a140358a61baeac4f3925c
Publikováno v:
Anesthésie & Réanimation. 4:290-299
Resume Chez l’enfant, et plus particulierement chez le nouveau-ne, les mecanismes complexes, qui permettent la prevention des hemorragies et des thromboses en associant l’action des plaquettes et de nombreuses proteines de la coagulation et de la
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e698e2dc0058ec7b30ed158e25c85e9
https://doi.org/10.1016/j.anrea.2018.03.013
https://doi.org/10.1016/j.anrea.2018.03.013
Autor:
Olivier Bourdon, Jérôme Naudin, Marie-Françoise Hurtaud-Roux, Ronan Bonnefoy, C. Farnoux, Julie Noailly, Theresa Kwon, S. Prot-Labarthe, Laily Sadozai
Publikováno v:
Archives of Disease in Childhood. 105:e30.1-e30
AimsEnoxaparin and tinzaparin, two low-molecular-weight heparins (LMWH), are used in paediatrics with multiples advantages such as facility of administration, reduced frequency of side effects, reduced drug interaction. However, their use is at highe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b68372d07f70a43f0a415cc0ccb5f00
https://doi.org/10.1136/archdischild-2020-nppg.54
https://doi.org/10.1136/archdischild-2020-nppg.54
Autor:
Paquita Nurden, Béatrice Saposnik, Marie-Françoise Hurtaud-Roux, Alan T. Nurden, Nicole Schlegel, Sylvie Binard, Odile Fenneteau
Publikováno v:
Molecular Genetics & Genomic Medicine
MYH9-Related Disorders are a group of rare autosomal dominant platelet disorders presenting as nonsyndromic forms characterized by macrothrombocytopenia with giant platelets and leukocyte inclusion bodies or as syndromic forms combining these hematol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb4ba557fa1986b5e797225db6637946
http://europepmc.org/articles/PMC4113270
http://europepmc.org/articles/PMC4113270
Autor:
Paula G. Heller, Loredana Bury, Catherine Trichet, Nuria Pujol-Moix, Alessandro Pecci, Fabrizio Fabris, Maria Luigia Randi, Ana C. Glembotsky, Marco Cattaneo, Adam Cuker, Jeanne-Yvonne Borg, Nathalie Trillot, James B. Bussel, Patrizia Noris, E Muniz-Diaz, François Lanza, Lucia Dora Notarangelo, Dominique Martin-Coignard, Anne Bauters, Paolo Gresele, Thomas Lecompte, Catherine Klersy, Sandra Mercier, Giuseppe Loffredo, Marie-Françoise Hurtaud-Roux, Véronique Le Cam Duchez, Emanuela Falcinelli, Nicole Schlegel, Erica De Candia, Dino Veneri, Schéhérazade Benabdallah-Guedira, Fanny Menard, Catherine Pouymayou, Ilaria Nichele, Chloé James, Michela Faleschini, Elisa Civaschi, Caterina Marconi, Roberta Bottega, Tommaso Pippucci, Pierre Sié, Sophie Bayart, Béatrice Saposnik, Daniela De Rocco, Rémi Favier, Françoise Boehlen, Pierre Fontana, Alina Ferster, Anna Savoia, Carlo L. Balduini, Pamela Magini, Bruno Royer, Véronique Latger-Cannard, Alessandra Tucci, Dominique Fleury, Agnes Rigouzzo, Tiziana Fierro, Gian Marco Podda, Emmanuel de Maistre, Silvia Ferrari, Paquita Nurden, Pietro Minuz, Andreas Greinacher, Virginie Siguret, A. M. Mezzasoma
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
HAEMATOLOGICA
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Haematologica, Vol. 99, No 8 (2014) pp. 1387-94
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
HAEMATOLOGICA
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Haematologica, Vol. 99, No 8 (2014) pp. 1387-94
Pregnancy in women with inherited thrombocytopenias is a major matter of concern as both the mothers and the newborns are potentially at risk of bleeding. However, medical management of this condition cannot be based on evidence because of the lack o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ee02baeb355d1552e96f4249ac1853e
http://hdl.handle.net/11368/2846527
http://hdl.handle.net/11368/2846527
Autor:
Sylvie Binard, Anne Vincenot, Olivier René, Nicole Schlegel, Marie-Françoise Hurtaud-Roux, Odile Fenneteau
Publikováno v:
Annales de biologie clinique. 74(3)
We report the identification of a new case of familial non syndromic severe thrombocytopenia. Bleeding was mild and no extra-haematological symptoms were found. Platelet morphology was normal as well as the quantitative expression of platelet membran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dbec729068ddd99b67ef6fcea40da3c
https://pubmed.ncbi.nlm.nih.gov/27108925
https://pubmed.ncbi.nlm.nih.gov/27108925
Autor:
Philippe Hubert, Véronique Baudouin, Marie-Françoise Hurtaud-Roux, Dominique Lasne, Fabrice Lesage
Publikováno v:
Hématologie. 18:233-238
hma.2012.0728 Auteur(s) : Marie-Francoise Hurtaud-Roux1, Dominique Lasne2, Veronique Baudouin3, Fabrice Lesage4, Philippe Hubert4 1 Laboratoire d’hematologie, hopital Robert-Debre, Paris 2 Laboratoire d’hematologie, hopital Necker, Paris 3 Servic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5db2bc07589bdd8173e915bdbabc0414
https://doi.org/10.1684/hma.2012.0728
https://doi.org/10.1684/hma.2012.0728
Autor:
Véronique Baudouin, Marie-Françoise Hurtaud-Roux, Odile Fenneteau, Blandine Bénet, Elodie Lainey
Publikováno v:
Annales de biologie clinique. 68:485-489
Arthrogryposis Renal Fanconi syndrome and Cholestasis (ARC syndrome) is an extremely rare disease (62 cases) and is uneasy to diagnose. This congenital multisystem disorder affects newborns who usually die in the first year of life. The three cases h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74c60ccd0c4f2df45f84ef89f91c2a13
https://doi.org/10.1684/abc.2010.0453
https://doi.org/10.1684/abc.2010.0453
Autor:
Marie-Françoise Hurtaud-Roux, Hadji Djaffar, Brigitte Llanas, Solène Evrard, Georges Deschênes, Theresa Kwon, Ferielle Louillet, Véronique Baudouin, Anis Larakeb
Publikováno v:
Pediatric Nephrology. 24:207-209
Although varicella is a common disease of childhood, renal complications are quite rare. We report here the interesting case of a-22 month-old boy exhibiting renal cortical necrosis related to an acquired protein S deficiency following varicella. Ten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73151a43382616f179ff89425fc6968e
https://doi.org/10.1007/s00467-008-0967-y
https://doi.org/10.1007/s00467-008-0967-y