Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Éliane Gluckman"'
Autor:
Éliane, Gluckman, Hanadi, Rafii
Publikováno v:
Soins; la revue de reference infirmiere. 66(854)
Bone marrow transplant, more recently called hematopoietic stem cell transplant (HSC), is a complex medical procedure in which a patient with or without malignant hematologic disease receives a combination of chemoradiation followed by an injection o
Publikováno v:
Leukemia. 36:599-600
Autor:
Graziana M. Scigliuolo, Wahid Boukouaci, Barbara Cappelli, Fernanda Volt, Monica M. Rivera Franco, Nathalie Dhédin, Regis Peffault deLatour, Christine Devalck, Jean‐Hugues Dalle, Martin Castelle, Olivier Hermine, Marie Ouachée Chardin, Xavier Poiré, Bénédicte Brichard, Catherine Paillard, Hanadi Rafii, Chantal Kenzey, Ching‐Lien Wu, Jihène Bouassida, Marie Robin, Nicole Raus, Vanderson Rocha, Annalisa Ruggeri, Eliane Gluckman, Ryad Tamouza, Eurocord and Société Francophone de Greffe de Moelle et de Thérapie Cellulaire (SFGM‐TC)
Publikováno v:
eJHaem, Vol 4, Iss 4, Pp 963-969 (2023)
Abstract The genetic diversity of the human leukocyte antigen (HLA) system was shaped by evolutionary constraints exerted by environmental factors. Analyzing HLA diversity may allow understanding of the underlying pathways and offer useful tools in t
Externí odkaz:
https://doaj.org/article/86ab1501991c49b0af0257f988a5fc8c
This text aims to provide simplified practical guidelines to start a hematopoietic stem cell transplantation unit which could be implemented in most centers and countries worldwide. The book also provides guidelines for existing transplantation units
Congenital and Acquired Bone Marrow Failure is a comprehensive guide to congenital and acquired bone marrow failure in adult and pediatric patients. Chapters are divided into two sections, acquired aplastic anemia and inherited bone marrow failure sy
Autor:
Ryad Tamouza, Fernanda Volt, Jean-Romain Richard, Ching-Lien Wu, Jihène Bouassida, Wahid Boukouaci, Pauline Lansiaux, Barbara Cappelli, Graziana Maria Scigliuolo, Hanadi Rafii, Chantal Kenzey, Esma Mezouad, Soumia Naamoune, Leila Chami, Florian Lejuste, Dominique Farge, Eliane Gluckman
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
Autism spectrum disorder (ASD) represents a set of heterogeneous neurodevelopmental conditions defined by impaired social interactions and repetitive behaviors. The number of reported cases has increased over the past decades, and ASD is now a major
Externí odkaz:
https://doaj.org/article/46e11a01020c4e32946b64e7a91d28f1
Autor:
Effie W. Petersdorf, Ted Gooley, Fernanda Volt, Chantal Kenzey, Alejandro Madrigal, Caroline McKallor, Sergio Querol, Hanadi Rafii, Vanderson Rocha, Ryad Tamouza, Christian Chabannon, Annalisa Ruggeri, Eliane Gluckman
Publikováno v:
Haematologica, Vol 106, Iss 12 (2020)
Cord blood transplantation (CBT) can cure life-threatening blood disorders. The HLA-B leader affects the success of unrelated donor transplantation but its role in CBT is unknown. We tested the hypothesis that the HLA-B leader influences CBT outcomes
Externí odkaz:
https://doaj.org/article/1b247e14d33f43df8055c490cf61c897
Autor:
Karina Tozatto-Maio, Robert Girot, Indou Deme Ly, Ana Cristina Silva Pinto, Vanderson Rocha, Francisco Fernandes, Ibrahima Diagne, Yahia Benzerara, Carla L. Dinardo, Julia Pavan Soler, Simone Kashima, Itauá Leston Araujo, Chantal Kenzey, Guilherme H. H. Fonseca, Evandra S. Rodrigues, Fernanda Volt, Luciana Jarduli, Annalisa Ruggeri, Christina Mariaselvam, Sandra F. M. Gualandro, Hanadi Rafii, Barbara Cappelli, Felipe Melo Nogueira, Graziana Maria Scigliuolo, Renato Luiz Guerino-Cunha, Kelen Cristina Ribeiro Malmegrim, Belinda P. Simões, Eliane Gluckman, Ryad Tamouza
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Sickle cell disease (SCD), the most common monogenic disease worldwide, is marked by a phenotypic variability that is, to date, only partially understood. Because inflammation plays a major role in SCD pathophysiology, we hypothesized that single nuc
Externí odkaz:
https://doaj.org/article/67cb8a7ed9504d0aaebc582eaf5a2b7d
Autor:
Christelle Rémus, Aurélie Stanislas, Naïm Bouazza, Valérie Gauthereau, Michel Polak, Stéphane Blanche, Assa Niakaté, Eliane Gluckman, Jean-Marc Tréluyer, Arnold Munnich, Robert Girot, Marina Cavazzana
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Aim: Sickle cell disease (SCD) is the most frequent monogenic disease worldwide; ~5–7% of the world population carry a hemoglobin disorder trait. In the US, one in every 1,941 newborns has SCD, whereas one in every 3,000 newborns in France is affec
Externí odkaz:
https://doaj.org/article/7b3f19d6c31544f0aefbb0c332664c4c
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