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Toux chronique de l'enfant

Autor: G. Benoist, G. Thouvenin

Publikováno v: Perfectionnement en Pédiatrie. 2:S51-S53

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e1a66b2829740698d916d4a5f495f5b0
https://doi.org/10.1016/s2588-932x(19)30190-1

Multidisciplinary advisory teams to manage multidrug-resistant tuberculosis: the example of the French Consilium

Autor: H. Guillot, G Thouvenin, J. Jaffré, Alexandra Aubry, Christine Bernard, Dhiba Marigot-Outtandy, B Henry, Valérie Pourcher, Florence Brossier, N. El Helali, Vincent Jarlier, D. Le Dû, Jérôme Robert, Nicolas Veziris, Laurent Raskine, B. Dautzenberg, Marie Jaspard, Claire Andrejak, B. Rivoire, Lorenzo Guglielmetti, Faiza Mougari, K. Chadelat, Mathilde Fréchet-Jachym

Publikováno v: International Journal of Tuberculosis and Lung Disease
International Journal of Tuberculosis and Lung Disease, International Union Against Tuberculosis and Lung Disease, 2019, 23 (10), pp.1050-1054. ⟨10.5588/ijtld.18.0779⟩

SETTING: The World Health Organization (WHO) recommends that multidrug-resistant tuberculosis (MDR-TB) treatment should be managed in collaboration with multidisciplinary advisory committees (consilia). A formal national Consilium has been establishe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8c9f2994a62790e0718d55ee1004a0d
https://pubmed.ncbi.nlm.nih.gov/31627767

Lung function in patients with Primary Ciliary Dyskinesia (PCD): a study from the international PCD (iPCD) Cohort

Autor: Halbeisen, Florian S., Goutaki, Myrofora, Spycher, Ben, Amirav, I., Behan, Laura, Boon, M., Hogg, Claire, Casaulta, C., Haarman, Eric G., Crowley, S., Karadag, Bulent, Koerner-Rettberg, C., Loebinger, Michael R., Mazurek, H., Morgan, Lucy, Nielsen, Kim G., Omran, Heymut, Santamaria, Francesca, Schwerk, N., G, Thouvenin, Yiallouros, Panayiotis, Lucas, Jane, Latzin, Philipp, Kuehni, Claudia E.

Primary ciliary dyskinesia (PCD) has been considered to be relatively mild disease, especially compared to cystic fibrosis (CF), but studies on lung function in PCD patients have been few and small. This study compared lung function from spirometry o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______348::c19412d1c3ff56849c4c4d53ce80bb7a
https://eprints.soton.ac.uk/422059/