Zobrazeno 1 - 10
of 389
pro vyhledávání: '"V. Colomb"'
Publikováno v:
Acta Horticulturae. :9-14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f16ca2c1e255573283fa258a84176565
https://doi.org/10.17660/actahortic.2017.1153.2
https://doi.org/10.17660/actahortic.2017.1153.2
Autor:
Christophe Marguet, M. Murris-Espin, Anne Munck, Dominique Hubert, V. Colomb-Jung, Harriet Corvol, Stéphanie Bui
Publikováno v:
Revue des Maladies Respiratoires. 33:658-665
Resume Introduction Le traitement de la mucoviscidose est reste longtemps symptomatique. Des therapeutiques ciblant la proteine CFTR defectueuse commencent a etre disponibles. Etat des connaissances Les resultats de la therapie genique restent modest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ceeece2f211c09d89e1a32d101eae66a
https://doi.org/10.1016/j.rmr.2015.11.010
https://doi.org/10.1016/j.rmr.2015.11.010
Autor:
Cécile Talbotec, Frank M. Ruemmele, Christophe Chardot, Yann Revillon, Florence Lacaille, Dominique Jan, S. Ganousse-Mazeron, Olivier Goulet, Danielle Canioni, V. Colomb-Jung, Frédérique Sauvat
Publikováno v:
Clinical Nutrition. 34:428-435
Chronic intestinal failure (CIF) requires long term parenteral nutrition (PN) and, in some patients, intestinal transplantation (ITx). Indications and timing for ITx remain poorly defined. In the present study we aimed to analyze causes and outcome o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9e46ab2392d0ef00bb04ba766e825db
https://doi.org/10.1016/j.clnu.2014.04.015
https://doi.org/10.1016/j.clnu.2014.04.015
Autor:
S, Bui, J, Macey, M, Fayon, T, Bihouée, P-R, Burgel, V, Colomb, H, Corvol, I, Durieu, D, Hubert, C, Marguet, E, Mas, A, Munck, M, Murris-Espin, P, Reix, I, Sermet-Gaudelus
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 23(12S)
Since the discovery of chloride secretion by the Cystic Fibrosis Transport regulator CFTR in 1983, and CFTR gene in 1989, knowledge about CFTR synthesis, maturation, intracellular transfer and function has dramatically expanded. These discoveries hav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b16d0e1a6cb5d041008892ff28469566
https://pubmed.ncbi.nlm.nih.gov/28231894
https://pubmed.ncbi.nlm.nih.gov/28231894
Autor:
V. Colomb
Publikováno v:
EMC - Pédiatrie - Maladies infectieuses. 4:1-8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6cd1bb8d01159eca1f34180333f21a5e
https://doi.org/10.1016/s1637-5017(09)72425-1
https://doi.org/10.1016/s1637-5017(09)72425-1
Autor:
V. Colomb
Publikováno v:
EMC - Pediatría. 44:1-6
El estado patologico de desnutricion siempre aparece como consecuencia de unos aportes inadecuados respecto a las necesidades. El nino es particularmente vulnerable, porque su crecimiento supone un considerable consumo de energia y de proteinas. En l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4965fbe09d287b3b31b0cee020cc26ed
https://doi.org/10.1016/s1245-1789(09)70194-5
https://doi.org/10.1016/s1245-1789(09)70194-5
Publikováno v:
Revue des maladies respiratoires. 33(8)
The treatment of cystic fibrosis has been symptom-based for a number of years. New therapies that aim to improve CFTR protein function are now emerging.The results of gene therapy has been modest but a recent clinical trial shows a positive effect on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0ead6000761891ff4a330b47ff2c8f07
https://pubmed.ncbi.nlm.nih.gov/26806675
https://pubmed.ncbi.nlm.nih.gov/26806675
Autor:
R. Kanaan, A.-S. Duflos, R. Panzo, E. Burnet, Daniel Dusser, J. Champreux, I. Honoré, Pierre-Régis Burgel, D. Huber, V. Colomb-Jung, C. Dupont
Publikováno v:
Journal of Cystic Fibrosis. 15:S103-S104
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::214e900691d26fa10e2c302fdf5b0444
https://doi.org/10.1016/s1569-1993(16)30445-3
https://doi.org/10.1016/s1569-1993(16)30445-3
Autor:
Bénédicte Pigneur, Laëtitia Marie Petit, Cécile Lambe, Olivier Goulet, Florence Lacaille, A. Acramel, E. Abi Nader, Amelia Rocha, V. Colomb-Jung, Catherine Poisson, Hélène Garnier-Lengliné, Odile Corriol, F. Talbotec
Publikováno v:
Nutrition Clinique et Métabolisme. 30:55-56
Introduction et but de l’etude La nutrition parenterale (NP) est la base de la prise en charge de l’insuffisance intestinale. Le but de cette etude est d’analyser, sur une periode de 14 ans, les indications de la NP a domicile (NPAD) des enfant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1fb22eb4fa58aea09a4be5f63b20d993
https://doi.org/10.1016/j.nupar.2016.01.022
https://doi.org/10.1016/j.nupar.2016.01.022
Autor:
Siobhán B. Carr, Lydie Lemonnier, Abaigeal D. Jackson, Lutz Naehrlich, Edward F. McKone, Ruth H. Keogh, V. Colomb, A. Zolin, J. van Rens, Cono Ariti
Publikováno v:
Journal of Cystic Fibrosis. 16:S20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d20678deb87db65b447dc2d9bee2ab8
https://doi.org/10.1016/s1569-1993(17)30221-7
https://doi.org/10.1016/s1569-1993(17)30221-7