Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Nawa Hachem"'
Autor:
Mansour Alkobtawi, Qui Trung Ngô, Nicolas Chapuis, Romain H. Fontaine, Mira El Khoury, Matthieu Tihy, Nawa Hachem, Aude Jary, Vincent Calvez, Michaela Fontenay, Vassilis Tsatsaris, Sélim Aractingi, Bénédicte Oulès
Publikováno v:
Communications Medicine, Vol 3, Iss 1, Pp 1-14 (2023)
Abstract Background Pregnant women and their fetuses are particularly susceptible to respiratory pathogens. How they respond to SARS-CoV-2 infection is still under investigation. Methods We studied the transcriptome and phenotype of umbilical cord bl
Externí odkaz:
https://doaj.org/article/127cbe8f27fa4f4e9dfcabddb82bc8ae
Autor:
Rita, Poch, Solenne, Le Louet, Zofia, Hélias-Rodzewicz, Nawa, Hachem, Geneviève, Plat, Mohamed-Aziz, Barkaoui, Hélène, Lapillonne, François, Delhommeau, Jean-François, Emile, Jean, Donadieu, Sébastien, Héritier
Publikováno v:
British journal of haematologyReferences. 194(4)
BRAF inhibitors are an effective treatment for BRAF
Autor:
Jean-François Emile, J. Donadieu, Zofia Hélias-Rodzewicz, Geneviève Plat, Nawa Hachem, Sébastien Héritier, Hélène Lapillonne, Rita Poch, Solenne Le Louet, Mohamed-Aziz Barkaoui, François Delhommeau
Publikováno v:
British Journal of Haematology
British Journal of Haematology, Wiley, 2021, 194 (4), pp.745-749. ⟨10.1111/bjh.17721⟩
British Journal of Haematology, 2021, 194 (4), pp.745-749. ⟨10.1111/bjh.17721⟩
British Journal of Haematology, Wiley, 2021, 194 (4), pp.745-749. ⟨10.1111/bjh.17721⟩
British Journal of Haematology, 2021, 194 (4), pp.745-749. ⟨10.1111/bjh.17721⟩
International audience; BRAF inhibitors are an effective treatment for BRAFV600E-mutated, risk-organ-positive Langerhans cell histiocytosis (RO+ LCH). However, cell-free BRAFV600E DNA often persists during therapy and recurrence frequently occurs aft
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f20a518fb21e1d9532ec7e4e413e4a85
https://hal.archives-ouvertes.fr/hal-03401846
https://hal.archives-ouvertes.fr/hal-03401846
Autor:
Eric Jeziorski, Yves Bertrand, Flore Sicre de Fontbrune, Virginie Gandemer, Blandine Beaupain, Frédéric Millot, Jean Donadieu, François Delhommeau, Jean-Alain Martignoles, Marie-Laure Couec, Claude Preudhomme, Laetitia Largeaud, Cecile Renard, Nathalie Aladjidi, Pierre-Simon Rohrlich, Wadih Abou Chahla, Claire Fieschi, Sophie Kaltenbach, Stéphane Blanche, Despina Moushous, Pierre Hirsch, Isabelle Meyts, Guy Leverger, Thomas Longval, Jean Louis Stephan, Vincent Barlogis, Aline Moignet Autrel, Fanny Fouyssac, Dalila Adjaoud, Marlène Pasquet, Olivier Tournilhac, Vahid Asnafi, Patrick Revy, Pascale Flandrin-Gresta, Christine Bellanné-Chantelot, Liana Carausu, Nawa Hachem, Thierry Leblanc, Hélène Lapillonne, Jean Soulier, Mira El-Khoury
Publikováno v:
Blood. 136:22-23
Introduction : Hematological complications (HC) as Aplastic anemia (AA) and myelodysplasia and acute leukemia (MDS/AL) are frequent and life threatening in patients with Shwachman Diamond Syndrome (SDS) with SBDS mutations. The therapy of such events