Zobrazeno 1 - 10
of 51
pro vyhledávání: '"BEAUCHAMP NICOUD, A"'
Autor:
Legrand, Ollivier, Simonin, Ghislaine, Beauchamp-Nicoud, Anne, Zittoun, Robert, Marie, Jean-Pierre
Publikováno v:
In Blood 1 August 1999 94(3):1046-1056
Autor:
Baudard, M, Beauchamp-Nicoud, A, Delmer, A, Rio, B, Blanc, C M, Zittoun, R, Marie, J P, Blanc, C (AUTHOR)
Publikováno v:
Leukemia (08876924). Oct99, Vol. 13 Issue 10, p1481-1490. 10p.
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:
Beauchamp-Nicoud, A., Morle, L., Lutz, H. U., Stammler, P., Agulles, O., Petermann-Khder, R., Iolascon, A., Silverio Perrotta, Cynober, T., Tchernia, G., Delaunay, J., Baudin-Creuza, V.
Publikováno v:
Europe PubMed Central
Scopus-Elsevier
Scopus-Elsevier
A patient with hereditary spherocytosis (HS) was found not to have red cell membrane protein 4.2. This rare form of HS, or 4.2 (-) HS, stems from mutations within the ELB42 or the EPB3 genes. The patient had long suffered from a gastric ulcer and imp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::99d53f73244e3029ad5ae30f2d69eb75
http://hdl.handle.net/11591/196244
http://hdl.handle.net/11591/196244
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
Autor:
A Beauchamp-Nicoud, Blanc Cm, Jean-Pierre Marie, Bernard Rio, Alain Delmer, Marion Baudard, Zittoun R
Publikováno v:
Leukemia. 13:1481-1490
We reviewed the reports of 784 consecutive patients admitted to our department for newly diagnosed acute myeloid leukemia (AML) over a 16-year period. Median, 5-year and 10-year overall survivals were 9. 5 months, 17.3% and 11.7% respectively. Induct
Autor:
null Beauchamp-Nicoud, null Schischmanoff, null Alloisio, null Boivin, null Parsons, null Mielot, null Tchernia, null Legrand, null Miraglia del Giudice, null Gasparini, null Iolascon, null Wickramasinghe, null Delaunay
Publikováno v:
British Journal of Haematology. 106:948-953
The CDAN2 gene, responsible for congenital dyserythropoietic anaemia, type II (CDA II), was recently mapped to 20q11.2. We report data on an additional member of a previously studied CDA II family. This member had always been regarded as haematologic
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:
Beauchamp Nicoud A, Schischmanoff PO, Alloisio N, Boivin P, Parsons SF, Mielot F, Tchernia G, Legrand A, Miraglia Del Giudice E, Gasparini P, Wickramasinghe SN, Delaunay J., IOLASCON, ACHILLE
Publikováno v:
British journal of haematology. 106(4)
The CDAN2 gene, responsible for congenital dyserythropoietic anaemia, type II (CDA II), was recently mapped to 20q11.2. We report data on an additional member of a previously studied CDA II family. This member had always been regarded as haematologic
Autor:
BEAUCHAMP NICOUD, A, Schischmanoff, Po, Alloisio, N, Boivin, P, Parsons, Sf, Mielot, F, Tchernia, G, Legrand, A, MIRAGLIA DEL GIUDICE, E, Gasparini, Paolo, Iolascon, A, Wickramasinghe, Sn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c9143fa041dc3300b60bc4cad4b9823b
https://hdl.handle.net/11368/1695520
https://hdl.handle.net/11368/1695520