Zobrazeno 1 - 10
of 141
pro vyhledávání: '"G, Rault"'
Autor:
D. Pougheon Bertrand, A. Fanchini, P. Lombrail, G. Rault, A. Chansard, N. Le Breton, C. Frenod, F. Milon, C. Heymes Royer, D. Segretain, M. Silber, S. Therouanne, J. Haesebaert, C. Llerena, P. Michel, Q. Reynaud
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-19 (2023)
Abstract Background The objective of the study was to elaborate a conceptual framework related to the domains of patient experience along the cystic fibrosis (CF) journey from the patients and parents of children with CF to inform the design of a pat
Externí odkaz:
https://doaj.org/article/0352ed5ad9654817b121952c02b63d76
Autor:
D. Pougheon Bertrand, A. Fanchini, P. Lombrail, G. Rault, A. Chansard, N. Le Breton, C. Frenod, F. Milon, C. Heymes-Royer, D. Segretain, M. Silber, S. Therouanne, J. Haesebaert, C. Llerena, P. Michel, Q. Reynaud
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-14 (2022)
Abstract Introduction In France, the cystic fibrosis (CF) care pathway is coordinated by multidisciplinary teams from specialised CF centres or transplant centres. It includes the care provided at home or out of hospital, risk prevention in daily lif
Externí odkaz:
https://doaj.org/article/3bc8161e29764781b42286e28de0011a
Publikováno v:
Physical Modelling in Geotechnics ISBN: 9780203743362
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89c2ff69b21f989fc38b3dd6b3c4052f
https://doi.org/10.1201/9780203743362-62
https://doi.org/10.1201/9780203743362-62
Autor:
L. Rakotoarisoa, L. Weiss, F. Lefebvre, M. Porzio, B. Ravoninjatovo, M. Abely, I. Danner-Boucher, S. Dubois, F. Troussier, A. Prevotat, G. Rault, L. Kessler
Publikováno v:
Journal of Cystic Fibrosis. 21:S74
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59acaf77e7c56b9cccdad503cfa50145
https://doi.org/10.1016/s1569-1993(22)00381-2
https://doi.org/10.1016/s1569-1993(22)00381-2
Publikováno v:
Respiratory Medicine and Research
Respiratory Medicine and Research, Elsevier, 2020, 78, pp.100757-. ⟨10.1016/j.resmer.2020.100757⟩
Respiratory Medicine and Research, Elsevier, 2020, 78, pp.100757-. ⟨10.1016/j.resmer.2020.100757⟩
Stenotrophomonas maltophilia is an emerging opportunistic pathogen. The increasing incidence is of particular concern in patients with cystic fibrosis (CF). Since 2012, the Western France has witnessed high annual prevalence of S. maltophilia coloniz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dee70cfa42be7fee684ef562d4bc10c1
https://hal.archives-ouvertes.fr/hal-03492261
https://hal.archives-ouvertes.fr/hal-03492261
Autor:
Corinne Alberti, Maxime Morsa, E. Le Roux, Rémi Gagnayre, G. Rault, D. Pougheon, V. David, A. Perrin
Publikováno v:
Journal of Cystic Fibrosis. 20:S52
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5691d6a4dcf1b28849043b9f9873ef3d
https://doi.org/10.1016/s1569-1993(21)01528-9
https://doi.org/10.1016/s1569-1993(21)01528-9
Autor:
Pierre Lombrail, D. Pougheon, A. Fanchini, C. Llerena, P. Michel, Quitterie Reynaud, G. Rault
Publikováno v:
Journal of Cystic Fibrosis. 19:S67
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ced86d15508fb83e2c4e3e028e8f14d
https://doi.org/10.1016/s1569-1993(20)30379-9
https://doi.org/10.1016/s1569-1993(20)30379-9
Autor:
N. Pellen, G. Bellis, G. Rault, L. Gueganton, C. Belleguic, E. Deneuville, H. Journel, S. Ramel, V. Scotet, C. Ferec
Publikováno v:
Journal of Cystic Fibrosis. 19:S55
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::158fc4c7bf2ec7c2cfd7245ff22d871c
https://doi.org/10.1016/s1569-1993(20)30340-4
https://doi.org/10.1016/s1569-1993(20)30340-4
Autor:
Michel Roussey, M.-L. Dalphin, Anne Munck, L. Weiss, C. Llerena, Jacques Brouard, A. Dirou, Laure Couderc, G. Rault, C. Bailly, M. Lebourgeois, N. Wizla, M. Renouil, Isabelle Sermet-Gaudelus, S. Vrielynck
Publikováno v:
Archives de Pédiatrie. 21:654-662
Resume Ces recommandations sont destinees a harmoniser les procedures concernant la prise en charge des nourrissons de moins de 2 ans atteints de formes typiques de mucoviscidose et diagnostiques par depistage neonatal. Elles ont ete elaborees par le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85df8b00be4090185a21e5a4c49ff4c9
https://doi.org/10.1016/j.arcped.2014.03.014
https://doi.org/10.1016/j.arcped.2014.03.014
Publikováno v:
Journal of Cystic Fibrosis. 18:S124
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1aa1e4f31fe7d2b44c42429cfe6cd79
https://doi.org/10.1016/s1569-1993(19)30530-2
https://doi.org/10.1016/s1569-1993(19)30530-2