Respiratory Status After Hematopoietic Stem Cell Transplantation for Primary Immunodeficiency

Autor: H. Salvator, A. Le Gal, A.-L. Brun, A. Marcais, C. Givel, F. Lanternier, C. Tcherakian, M. Cheminant, C. Goyard, B. Neven, A. Chabrol, D. Moshous, E. Caradec, A. Fischer, O. Lortholary, O. Hermine, N. Mahlaoui, F. Suarez, L.-J. Couderc, E. Catherinot

Publikováno v: C34. SARCOIDOSIS, FIBROSIS, AND PROTEINOSIS - OH MY!.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::46b67904536d42c9122968c1d413f90e
https://doi.org/10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a4827

The first steps towards a diverse and inclusive EBMT: a position paper

Autor: S. Montoto, J. A. Snowden, C. Chabannon, S. Corbacioglu, R. de la Camara, H. Dolstra, R. Greco, A. Gusi, N. Hamad, M. Kenyon, N. Kröger, M. Mohty, J. Murray, A. Mueller, B. Neven, R. Peffault de Latour, Z. Peric, I. Sánchez-Ortega, A. Sureda, B. Verhoeven, A. Villar, I. Yakoub-Agha

Publikováno v: Bone Marrow Transplantation
Bone Marrow Transplantation, 2022, ⟨10.1038/s41409-022-01586-w⟩
Bone Marrow Transplantation, 57, 3, pp. 343-346
Bone Marrow Transplantation, 57, 343-346

Contains fulltext : 248819.pdf (Publisher’s version ) (Open Access)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78f62efad8048ec651ff57d9f7cfbb4d
https://hal.sorbonne-universite.fr/hal-03561399/document

Atteintes neurologiques multifacettes des déficits en CTLA4 : étude observationnelle nationale

Autor: C. Coustal, R. Goulabchand, P. Labauge, P. Guilpain, C. Carra-Dallière, E. Januel, E. Jeziorski, V. Salle, J.F. Viallard, D. Boutboul, C. Fieschi, D. Gobert, N. Aladjidi, P. Rullier, J. Graveleau, M.L. Piel-Julian, F. Suarez, B. Neven, N. Mahlaoui, X. Ayrignac

Publikováno v: La Revue de Médecine Interne. 43:A408

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1ca2d31d5ae9dba7ac41eff0255095db
https://doi.org/10.1016/j.revmed.2022.10.135

Cutaneous granulomas with primary immunodeficiency in children: a report of 17 new patients and a review of the literature

Autor: Capucine Picard, D Moshous, Nizar Mahlaoui, A Fischer, C Bodemer, Sylvie Fraitag, S Blanche, Philippe Pérot, Ludovic Martin, B Neven, Stéphanie Leclerc-Mercier, Isabelle Pellier, Marc Eloit

Publikováno v: Journal of the European Academy of Dermatology and Venereology
Journal of the European Academy of Dermatology and Venereology, Wiley, 2019, 33 (7), pp.1412-1420. ⟨10.1111/jdv.15568⟩
Journal of the European Academy of Dermatology and Venereology, 2019, 33 (7), pp.1412-1420. ⟨10.1111/jdv.15568⟩

International audience; BACKGROUND: Paediatric cutaneous granuloma with primary immunodeficiency (PID) is a rare condition. The physiopathology is unclear, and treatment is challenging. We report on 17 paediatric cases and review the literature.OBJEC

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c70128c4f54259c1c08c41055f17d7e
https://doi.org/10.1111/jdv.15568

[Hurler syndrome: early diagnosis and treatment]

Autor: S, Leroux, J-B, Muller, E, Boutaric, A, Busnel, F, Lemouel, M, Andro-Garçon, B, Neven, V, Valayannopoulos, C, Vinceslas

Publikováno v: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 21(5)

Hurler syndrome, the most severe form of mucopolysaccharidosis type I (MPS I), is a rare lysosomal storage disease. The overall incidence of MPS I is 0.99-1.99/100,000 live births. Accumulation of glycosaminoglycans causes the progressive dysfunction

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9a9fb16bfd3f5cd81ac9117b8e79cdbb
https://pubmed.ncbi.nlm.nih.gov/24698225