Evaluation of quantitative PCR for early diagnosis of Pseudomonas aeruginosa infection in cystic fibrosis: a prospective cohort study
Héry-Arnaud, G., Nowak, E., Caillon, J., David, V., Dirou, A., Revert, K., Munck, M.-R., Frachon, I., Haloun, A., Horeau-Langlard, D., Le Bihan, J., Danner-Boucher, I., Ramel, S., Pelletier, M.-P., Rosec, S., Gouriou, S., Poulhazan, E., Payan, C., Férec, C., Rault, G., Le Gal, G., Le Berre, R.
Published in Clinical microbiology and infection (01.03.2017)
Published in Clinical microbiology and infection (01.03.2017)
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Frequency of aquagenic palmoplantar keratoderma in cystic fibrosis: a new sign of cystic fibrosis?
Garçon-Michel, N., Roguedas-Contios, A.-M., Rault, G., Le Bihan, J., Ramel, S., Revert, K., Dirou, A., Misery, L.
Published in British journal of dermatology (1951) (01.07.2010)
Published in British journal of dermatology (1951) (01.07.2010)
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275 A quality improvement program (QIP) aimed at improving nutritional status of cystic fibrosis (CF) patients aged 2–12 years at CF Centre Roscoff: Update at the end of the 3 year period
Revert, K, Pengam, J, Madec, M.-L, Audran, L, Maitrallin, L, Lesné, P
Published in Journal of cystic fibrosis (01.06.2015)
Published in Journal of cystic fibrosis (01.06.2015)
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WS20.4 Real-time PCR (RT-PCR) provides a “window of opportunity”: optimal screening of patients with cystic fibrosis (CF) through an earlier detection of Pseudomonas aeruginosa (PA)
Hérv-Arnaud, G, Nowak, E, Le Gall, F, Rosec, S, Caillon, J, David, V, Danner, I, Dirou, A, Frachon, I, Haloun, A, Horeau-Langlard, D, Le Bihan, J, Munck, M.-R, Pelletier, M.-P, Quiot, J.-J, Ramel, S, Rault, G, Revert, K, Poulhazan, E, Payan, C, Le Berre, R
Published in Journal of cystic fibrosis (01.06.2012)
Published in Journal of cystic fibrosis (01.06.2012)
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Singing and Cystic Fibrosis: A pilot experience at Centre de Perharidy (Roscoff, France)
Dirou, A, Cueff, E, Lejosne, C, Guéganton, L.J, Revert, K, Rault, G
Published in Journal of cystic fibrosis (2009)
Published in Journal of cystic fibrosis (2009)
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279 A quality improvement program (QIP) aimed at improving nutritional status of CF patients aged 2-12 years old over a 3 year period at CF Centre Roscoff
Revert-Murnaghan, K, Pengam, J, Madec, M.-L, Audran, L, Jaffrennou, S, Maitrallain, L, Naud, A, Lesne, P
Published in Journal of cystic fibrosis (01.06.2012)
Published in Journal of cystic fibrosis (01.06.2012)
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31 Feasibility of 1H-NMR spectroscopy to detect occurrence of Pseudomonas aeruginosa in saliva of cystic fibrosis patients
Rivas, R., Cerantola, S., Barbier, G., Revert, K., Gouriou, S., Rault, G., Boisramé-Gastrin, S.
Published in Journal of cystic fibrosis (01.06.2014)
Published in Journal of cystic fibrosis (01.06.2014)
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Journal Article
Frequency of aquagenic palmoplantar keratoderma in cystic fibrosis: a new sign of cystic fibrosis?: Aquagenic palmoplantar keratoderma in cystic fibrosis
Garçon-Michel, N., Roguedas-Contios, A.-M., Rault, G., Le Bihan, J., Ramel, S., Revert, K., Dirou, A., Misery, L.
Published in British journal of dermatology (1951) (01.07.2010)
Published in British journal of dermatology (1951) (01.07.2010)
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Hidradénite plantaire et mucoviscidose
Eusen, M., Abasq, C., Lemasson, G., Revert, K., Misery, L.
Published in Annales de dermatologie et de vénéréologie (01.12.2011)
Published in Annales de dermatologie et de vénéréologie (01.12.2011)
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