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Page 1
Emergency management of patients with Glanzmann thrombasthenia: consensus recommendations from the French reference center for inherited platelet disorders.
Fiore M, Giraudet JS, Alessi MC, Falaise C, Desprez D, d'Oiron R, Voisin S, Hurtaud MF, Boutroux H, Saultier P, Lavenu-Bombled C, Bagou G, Dubucs X, Chauvin A, Leroy C, Meckert F, Kerbaul F, Giraud N, Pühler A, Rath A. Fiore M, et al. Among authors: boutroux h. Orphanet J Rare Dis. 2023 Jun 29;18(1):171. doi: 10.1186/s13023-023-02787-2. Orphanet J Rare Dis. 2023. PMID: 37386449 Free PMC article. Review.
Leukemia Cutis in Childhood Acute Myeloid Leukemia: Epidemiological, Clinical, Biological, and Prognostic Characteristics of Patients Included in the ELAM02 Study.
Gouache E, Greze V, Strullu M, Saultier P, Fenneteau O, Gandemer V, Ragu C, Auvrignon A, Boutroux H, Lapillonne H, Pasquet M, Leverger G. Gouache E, et al. Among authors: boutroux h. Hemasphere. 2018 Oct;2(5):e141. doi: 10.1097/HS9.0000000000000141. Epub 2018 Oct 2. Hemasphere. 2018. PMID: 30887005 Free PMC article. No abstract available.
Germline RUNX1 variants in paediatric patients in a French specialised centre.
Liu C, Ballerini P, Nguyen G, Mincheva Z, Copin B, Bouslama B, Leverger G, Petit A, Favier R, Lapillonne H, Boutroux H. Liu C, et al. Among authors: boutroux h. EJHaem. 2022 Nov 6;4(1):145-152. doi: 10.1002/jha2.594. eCollection 2023 Feb. EJHaem. 2022. PMID: 36819173 Free PMC article.
Is Acute Myeloblastic Leukemia in Children Under 2 Years of Age a Specific Entity? A Report from the FRENCH ELAM02 Study Group.
Blais S, Boutroux H, Pasquet M, Leblanc T, Fenneteau O, Gandemer V, Bertrand Y, Ducassou S, Michel G, Nelken B, Petit A, Cuccuini W, Gouache E, Renaut MA, Baruchel A, Lapillonne H, Leverger G. Blais S, et al. Among authors: boutroux h. Hemasphere. 2019 Oct 30;3(6):e316. doi: 10.1097/HS9.0000000000000316. eCollection 2019 Dec. Hemasphere. 2019. PMID: 31976488 Free PMC article.
Rhabdomyosarcoma associated with germline TP53 alteration in children and adolescents: The French experience.
Pondrom M, Bougeard G, Karanian M, Bonneau-Lagacherie J, Boulanger C, Boutroux H, Briandet C, Chevreau C, Corradini N, Coze C, Defachelles AS, Galmiche-Roland L, Orbach D, Piguet C, Scoazec JY, Vérité C, Willems M, Frebourg T, Minard V, Brugières L. Pondrom M, et al. Among authors: boutroux h. Pediatr Blood Cancer. 2020 Sep;67(9):e28486. doi: 10.1002/pbc.28486. Epub 2020 Jul 13. Pediatr Blood Cancer. 2020. PMID: 32658383 Clinical Trial.
Integrative clinical and biopathology analyses to understand the clinical heterogeneity of infantile rhabdomyosarcoma: A report from the French MMT committee.
Butel T, Karanian M, Pierron G, Orbach D, Ranchere D, Cozic N, Galmiche L, Coulomb A, Corradini N, Lacour B, Proust S, Guerin F, Boutroux H, Rome A, Mansuy L, Vérité C, Defachelles AS, Tirode F, Minard-Colin V. Butel T, et al. Among authors: boutroux h. Cancer Med. 2020 Apr;9(8):2698-2709. doi: 10.1002/cam4.2713. Epub 2020 Feb 22. Cancer Med. 2020. PMID: 32087612 Free PMC article.
Polycomb repressive complex 2 haploinsufficiency identifies a high-risk subgroup of pediatric acute myeloid leukemia.
Bond J, Labis E, Marceau-Renaut A, Duployez N, Labopin M, Hypolite G, Michel G, Ducassou S, Boutroux H, Nelken B, Bertrand Y, Baruchel A, Petit A, Asnafi V, Leverger G, Preudhomme C, Macintyre E, Lapillonne H. Bond J, et al. Among authors: boutroux h. Leukemia. 2018 Aug;32(8):1878-1882. doi: 10.1038/s41375-018-0187-9. Epub 2018 Jun 27. Leukemia. 2018. PMID: 29950694 No abstract available.
23 results