Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Cecile Arnaud"'
Autor:
Valentine Brousse, Corinne Pondarre, Manoelle Kossorotoff, Cecile Arnaud, Annie Kamdem, Mariane de Montalembert, Benedicte Boutonnat-Faucher, Slimane Allali, Hélène Bourdeau, Keyne Charlot, Sebastien Bertil, Lydie da Costa, Philippe Connes, David Grévent, Suzanne Verlhac
Publikováno v:
Haematologica, Vol 107, Iss 4 (2021)
Despite its high prevalence in children with sickle cell anemia (SCA), the pathophysiology of silent cerebral infarcts (SCI) remains elusive. The main objective of this study was to explore the respective roles of major determinants of brain perfusio
Externí odkaz:
https://doaj.org/article/968055d9b80d4960b3e0f41232181235
Autor:
Valentine Brousse, Yves Colin, Catia Pereira, Cecile Arnaud, Marie Helene Odièvre, Anne Boutemy, Corinne Guitton, Mariane de Montalembert, Claudine Lapouméroulie, Julien Picot, Caroline Le Van Kim, Wassim El Nemer
Publikováno v:
EBioMedicine, Vol 2, Iss 2, Pp 154-157 (2015)
Sickle cell anaemia (SCA) results from a single mutation in the β globin gene. It is seldom symptomatic in the first semester of life. We analysed the expression pattern of 9 adhesion molecules on red blood cells, in a cohort of 54 SCA and 17 non-SC
Externí odkaz:
https://doaj.org/article/68773e3548734306bb42a7a40d3203b1
Autor:
Hanadi Rafii, Françoise Bernaudin, Helene Rouard, Valérie Vanneaux, Annalisa Ruggeri, Marina Cavazzana, Valerie Gauthereau, Aurélie Stanislas, Malika Benkerrou, Mariane De Montalembert, Christele Ferry, Robert Girot, Cecile Arnaud, Annie Kamdem, Joelle Gour, Claudine Touboul, Audrey Cras, Mathieu Kuentz, Claire Rieux, Fernanda Volt, Barbara Cappelli, Karina T. Maio, Annalisa Paviglianiti, Chantal Kenzey, Jerome Larghero, Eliane Gluckman
Publikováno v:
Haematologica, Vol 102, Iss 6 (2017)
Efforts to implement family cord blood banking have been developed in the past decades for siblings requiring stem cell transplantation for conditions such as sickle cell disease. However, public banks are faced with challenging decisions about the u
Externí odkaz:
https://doaj.org/article/cca9a98c47bd4c8cb0d56dc52d044a73
Autor:
Francoise Bernaudin, Robert C. Strunk, Annie Kamdem, Cecile Arnaud, Ping An, Martine Torres, Christophe Delacourt, Michael R. DeBaun
Publikováno v:
Haematologica, Vol 93, Iss 12 (2008)
Externí odkaz:
https://doaj.org/article/8210e6a21d304d1382db2e1c593f1b8e
Autor:
Claire Falguière, Slimane Allali, Bassem Khazem, Annie Kamdem, Cécile Arnaud, Marie Belloy, Corinne Guitton, Marie-Hélène Odièvre, Sophie Pertuisel, Cecile Dumesnil, Cécile Guillaumat, Nathalie Garrec, Alexandra Gauthier, Perrine Mahe, Valerie Soussan-Banini, Laure Le-Carrer, Etienne Merlin, Audrey David, Beatrice Pellegrino, Catherine Paillard, Jean-Francois Brasme, Marie Lagarde, France Pirenne, Corinne Pondarre
Publikováno v:
Haematologica, Vol 108, Iss 3 (2022)
Externí odkaz:
https://doaj.org/article/55f34e53da9c4d878fc44b17019665a0
Autor:
Françoise Bernaudin, Cécile Arnaud, Annie Kamdem, Isabelle Hau, Fouad Madhi, Camille Jung, Ralph Epaud, Suzanne Verlhac
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
The risk of stroke in children with sickle cell disease (SCD) is detected by abnormal intracranial arterial time-averaged mean of maximum velocities (TAMVs ≥200 cm/s). Recently, extracranial internal carotid artery (eICA) arteriopathy has been repo
Externí odkaz:
https://doaj.org/article/15730c2e84484b43b3c271894b72b84e
Akademický článek
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Autor:
Sara El Hoss, Sylvie Cochet, Mickaël Marin, Claudine Lapouméroulie, Michael Dussiot, Naïm Bouazza, Caroline Elie, Mariane de Montalembert, Cécile Arnaud, Corinne Guitton, Béatrice Pellegrino, Marie Hélène Odièvre, Frédérique Moati, Caroline Le Van Kim, Yves Colin Aronovicz, Wassim El Nemer, Valentine Brousse
Publikováno v:
Blood Advances, Vol 3, Iss 15, Pp 2328-2336 (2019)
Abstract: Spleen dysfunction is central to morbidity and mortality in children with sickle cell anemia (SCA). The initiation and determinants of spleen injury, including acute splenic sequestration (ASS) have not been established. We investigated spl
Externí odkaz:
https://doaj.org/article/689d734e554b4a85bbc751b1ba0bcfcf
Autor:
Alessandra Magnani, Corinne Pondarré, Naïm Bouazza, Jeremy Magalon, Annarita Miccio, Emmanuelle Six, Cecile Roudaut, Cécile Arnaud, Annie Kamdem, Fabien Touzot, Aurélie Gabrion, Elisa Magrin, Chloé Couzin, Mathieu Fusaro, Isabelle André, Jean-Paul Vernant, Eliane Gluckman, Françoise Bernaudin, Dominique Bories, Marina Cavazzana
Publikováno v:
Haematologica, Vol 105, Iss 5 (2020)
Although studies of mixed chimerism following hematopoietic stem cell transplantation in patients with sickle cell disease (SCD) may provide insights into the engraftment needed to correct the disease and into immunological reconstitution, an extensi
Externí odkaz:
https://doaj.org/article/5e2e03a1b4074479877aa42ad2bc5785
Autor:
Françoise Bernaudin, Cécile Arnaud, Annie Kamdem, Isabelle Hau, Françoise Lelong, Ralph Epaud, Corinne Pondarré, Serge Pissard
Publikováno v:
Blood Advances, Vol 2, Iss 6, Pp 626-637 (2018)
Abstract: Sickle cell anemia (SCA), albeit monogenic, has heterogeneous phenotypic expression, mainly related to the level of hemoglobin F (HbF). No large cohort studies have ever compared biological parameters in patients with major β-globin haplot
Externí odkaz:
https://doaj.org/article/ed7f3ecee6494156b33498d769cf1473