Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Anne Beauchamp-Nicoud"'
Autor:
Anne Beauchamp-Nicoud, Madeleine Fénéant-Thibault, Brigitte Bader-Meunier, Jean Delaunay, Thérèse Cynober, Gil Tchernia
Publikováno v:
The Hematology Journal. 5:S191-S194
Key words Name of the disease and synonyms Definition/diagnostic criteria Etiology Biological methods of diagnosis Incidence Management and treatments Unresolved questions and comments References Abstract Congenital dyserythropoietic anemias (CDA) re
Autor:
Gil Tchernia, Alain Bernheim, Claude Léonard, Serge Koscielny, Danielle Feneux, C Bayle, Anne Beauchamp-Nicoud, Jean-Henri Bourhis
Publikováno v:
British Journal of Haematology. 122:109-117
Summary. To evaluate the incidence and the predictive signs of therapy-related myelodysplasia and/or acute myeloid leukaemia (tMDS/tAML), we undertook a prospective study over a 4-year period of 221 patients who underwent autologous haematopoietic pr
Publikováno v:
Blood. 94:1046-1056
In adult acute myeloid leukemia (AML), the weight of the contribution of the combined activity of Pgp and MRP1 to drug resistance is not known. To address this question, we compared the activity of these proteins to the in vitro resistance to daunoru
Autor:
Anne, Beauchamp-Nicoud, Lydie, Da Costa, Alexis, Proust, Patricia, Rincé, Safa, Saker, Gil, Tchernia
Publikováno v:
Journal of pediatric hematology/oncology. 26(12)
Diamond-Blackfan anemia (DBA) is a rare etiology for congenital anemia, but this diagnosis should be considered when aregenerative hypoplastic anemia occurs in infancy. A term infant girl received a red blood cell transfusion at birth for neonatal an
Autor:
Anne, Beauchamp-Nicoud, Danielle, Feneux, Chantal, Bayle, Alain, Bernheim, Claude, Léonard, Serge, Koscielny, Gil, Tchernia, Jean-Henri, Bourhis
Publikováno v:
British journal of haematology. 122(1)
To evaluate the incidence and the predictive signs of therapy-related myelodysplasia and/or acute myeloid leukaemia (tMDS/tAML), we undertook a prospective study over a 4-year period of 221 patients who underwent autologous haematopoietic progenitor
Autor:
Anne Beauchamp-Nicoud, Nadia Arzouk, Georges Mourad, Renaud Snanoudj, Gil Tchernia, Bernard Charpentier, Antoine Durrbach
Publikováno v:
Transplant International. 19
Human parvovirus B19 (PVB 19) is responsible for pure red cell aplasia in immunocompromised patients, and particularly solid organ recipients. Intravenous immunoglobulins (IVIG) have been shown to be efficient to achieve the correction of anemia in a