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of 4
pro vyhledávání: '"Delphine Michon"'
Autor:
Malika Mahloul, Jacques de Blic, Annick Clement, Delphine Michon, Natacha Remus, Jean-François Vibert, Nadia Nathan
Publikováno v:
B57. RECOGNIZING AND MANAGING UNCOMMON LUNG DISEASES.
Autor:
A. Lemaire, J.-F. Vibert, Delphine Michon, Harriet Corvol, Aline Tamalet, Annick Clement, A. Blondel, Malika Mahloul, Delphine Feldmann, Brigitte Fauroux
Publikováno v:
Journal of Cystic Fibrosis. 8:S66
Autor:
Guillaume Aubertin, Brigitte Fauroux, Nadia Nathan, Malika Mahloul, Delphine Michon, Annick Clement, Jean-François Vibert, Nathalie Guillemot, Harriet Corvol
Publikováno v:
ResearcherID
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93c58331b918b3dfc8aab2a58b77c2aa
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000208770306412&KeyUID=WOS:000208770306412
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000208770306412&KeyUID=WOS:000208770306412
Autor:
Marc Lubrano, Pierrick Cros, Malika Mahloul, Antoine Deschildre, Nadia Nathan, M. Fayon, Harriet Corvol, Jacques de Blic, Philippe Reix, Françoise Troussier, Ralph Epaud, Annick Clement, Jessica Taytard, Raphaël Chiron, Delphine Michon
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 2013, 8 (1), pp.161. ⟨10.1186/1750-1172-8-161⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2013, 8 (1), pp.161. 〈10.1186/1750-1172-8-161〉
ResearcherID
Orphanet Journal of Rare Diseases, BioMed Central, 2013, 8 (1), pp.161. ⟨10.1186/1750-1172-8-161⟩
Orphanet Journal of Rare Diseases, 2013, 8 (1), pp.161. ⟨10.1186/1750-1172-8-161⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2013, 8 (1), pp.161. 〈10.1186/1750-1172-8-161〉
ResearcherID
Orphanet Journal of Rare Diseases, BioMed Central, 2013, 8 (1), pp.161. ⟨10.1186/1750-1172-8-161⟩
Background Idiopathic pulmonary hemosiderosis (IPH) is a rare cause of alveolar hemorrhage in children and its pathophysiology remains obscure. Classically, diagnosis is based on a triad including hemoptysis, diffuse parenchymal infiltrates on chest