Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Chantal Andriamanga"'
Autor:
Nicole Brousse, Felipe Suarez, Alain Fischer, Danielle Canioni, Jean-Philippe Jais, Olivier Hermine, Nizar Mahlaoui, Catherine Dubois d'Enghien, Chantal Andriamanga, Dominique Stoppa-Lyonnet
Publikováno v:
Journal of Clinical Oncology. 33:202-208
Purpose Biallelic mutations in ATM cause ataxia-telangiectasia (AT), a rare inherited disease with a high incidence of cancer. Precise estimates of the risk, presentation, and outcomes of cancer in patients with AT need to be addressed in large serie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8277fbedc9c400b2ec7e4eeed97d4878
https://doi.org/10.1200/jco.2014.56.5101
https://doi.org/10.1200/jco.2014.56.5101
Autor:
Dominique Stoppa-Lyonnet, Catherine Dubois d'Enghien, Jean-Philippe Jais, Danielle Canioni, Alain Fischer, Nizar Mahlaoui, Nicole Brousse, Chantal Andriamanga, Olivier Hermine, Felipe Suarez
Publikováno v:
Blood. 124:1634-1634
Introduction Ataxia-telangiectasia (A-T) is a rare autosomal recessive disorder associated with mutations in the ATMgene and characterized by cerebellar ataxia, telangiectasia, immune defect, and a high incidence of lymphoid and solid cancers. We con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da64c3f440fe3acfcde7dbb992f31b26
https://doi.org/10.1182/blood.v124.21.1634.1634
https://doi.org/10.1182/blood.v124.21.1634.1634
Autor:
Alain Fischer, Laetitia Compain, Nizar Mahlaoui, Hugo Chapdelaine, Chantal Andriamanga, Felipe Suarez, Olivier Hermine
Publikováno v:
Blood. 120:1057-1057
Abstract 1057 Background: Primary immunodeficiencies (PID) are rare congenital disorders involving defects of the immune system. Aside from infectious complications, patients are at increased risk of malignant complications, which represent a leading
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be5cb4115b60edc28079bcfe72922e23
https://doi.org/10.1182/blood.v120.21.1057.1057
https://doi.org/10.1182/blood.v120.21.1057.1057
Publikováno v:
International Journal of Technology Assessment in Health Care; 2023, Vol. 39 Issue 1, p1-8, 8p, 3 Charts
Publikováno v:
International Journal of Technology Assessment in Health Care; 2022, Vol. 38 Issue 1, p1-10, 10p, 2 Diagrams, 2 Charts
Publikováno v:
International Journal of Technology Assessment in Health Care; 2021, Vol. 38 Issue 1, p1-10, 10p
Autor:
Dunogué, Bertrand, Pilmis, Benoit, Mahlaoui, Nizar, Elie, Caroline, Coignard-Biehler, Hélène, Amazzough, Karima, Noël, Nicolas, Salvator, Hélène, Catherinot, Emilie, Couderc, Louis-Jean, Sokol, Harry, Lanternier, Fanny, Fouyssac, Fanny, Bardet, Julie, Bustamante, Jacinta, Gougerot-Pocidalo, Marie-Anne, Barlogis, Vincent, Masseau, Agathe, Durieu, Isabelle, Lecuit, Marc
Publikováno v:
Clinical Infectious Diseases; 3/15/2017, Vol. 64 Issue 6, p767-775, 9p, 5 Charts, 2 Graphs
Autor:
Odnoletkova, Irina1,2,3 irina.v.odnoletkova@gmail.com, Kindle, Gerhard4,5 gerhard.kindle@uniklinik-freiburg.de, Quinti, Isabella6,7 Isabella.quinti@uniroma1.it, Grimbacher, Bodo5,8 bodo.grimbacher@uniklinik-freiburg.de, Knerr, Viviane4,5 VivianeKnerr@gmx.de, Gathmann, Benjamin4,5 benjamin.gathmann@gmail.com, Ehl, Stephan4,5 stephan.ehl@uniklinik-freiburg.de, Mahlaoui, Nizar9,10,11 nizar.mahlaoui@nck.aphp.fr, Van Wilder, Philippe3 philippe.van.wilder@ulb.ac.b, Bogaerts, Kris12,13 Kris.bogaerts@kuleuven.be, de Vries, Esther14,15 esther.devries@etz.nl, Plasma Protein Therapeutics Association (PPTA) Taskforce
Publikováno v:
Orphanet Journal of Rare Diseases. 11/12/2018, Vol. 13 Issue 1, pN.PAG-N.PAG. 1p.
Autor:
Julie Bardet, Olivier Hermine, Fanny Lanternier, Nicolas Noel, Isabelle Durieu, Agathe Masseau, Olivier Lortholary, Felipe Suarez, Jacinta Bustamante, Bertrand Dunogue, Hélène Salvator, Benoit Pilmis, Marie-Anne Gougerot-Pocidalo, Stéphane Blanche, Fanny Fouyssac, Nizar Mahlaoui, Marc Lecuit, Harry Sokol, Emilie Catherinot, Vincent Barlogis, Caroline Elie, Alain Fischer, Louis-Jean Couderc, Hélène Coignard-Biehler, Karima Amazzough
Publikováno v:
Clinical Infectious Diseases
Clinical Infectious Diseases, Oxford University Press (OUP), 2017, 64 (6), pp.767-775. ⟨10.1093/cid/ciw837⟩
Clinical Infectious Diseases, 2017, 64 (6), pp.767-775. ⟨10.1093/cid/ciw837⟩
Clinical Infectious Diseases, Oxford University Press (OUP), 2017, 64 (6), pp.767-775. ⟨10.1093/cid/ciw837⟩
Clinical Infectious Diseases, 2017, 64 (6), pp.767-775. ⟨10.1093/cid/ciw837⟩
International audience; Background : Although prognosis of Chronic Granulomatous Disease (CGD) has greatly improved, few studies have focused on its long-term outcome. We studied the clinical course and sequelae of CGD patients diagnosed before age 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79c1c8f0a76ad14b2544dab1bebdebd5
https://doi.org/10.1093/cid/ciw837
https://doi.org/10.1093/cid/ciw837
