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Orphanet Journal of Rare Diseases|April 8, 2025
The RaDiCo information system for rare disease cohortsPaul Landais, Sonia Gueguen, Annick Clement, et al.Orphanet Journal of Rare Diseases|October 30, 2021
RaDiCo, the French national research program on rare disease cohortsSerge Amselem, Sonia Gueguen, Jérôme Weinbach, et al.Paediatric Respiratory Reviews|June 2, 2015
Biomarkers in Interstitial lung diseasesNadia Nathan, Harriet Corvol, Serge Amselem, et al.The International Journal of Biochemistry & Cell Biology|November 13, 2016
Surfactant protein A: A key player in lung homeostasisNadia Nathan, Jessica Taytard, Philippe Duquesnoy, et al.The International Journal of Biochemistry & Cell Biology|August 31, 2013
Alveolar epithelial cells: master regulators of lung homeostasisLoïc Guillot, Nadia Nathan, Olivier Tabary, et al.Molecular and Cellular Endocrinology|November 15, 2002
Current approaches for deciphering the molecular basis of combined anterior pituitary hormone deficiency in humansSerge AmselemThe Journal of Clinical Endocrinology and Metabolism|July 7, 2005
Functional relationship between LHX4 and POU1F1 in light of the LHX4 mutation identified in patients with pituitary defectsKalotina Machinis, Serge AmselemRespiration; International Review of Thoracic Diseases|September 13, 2021
Impact of Gender on the Characteristics of Patients with Idiopathic Pulmonary Fibrosis Included in the RaDiCo-ILD CohortVincent Cottin, Sonia Gueguen, Stéphane Jouneau, et al.ERJ Open Research|July 31, 2019
Bi-allelic missense ABCA3 mutations in a patient with childhood ILD who reached adulthoodEffrosyni D Manali, Marie Legendre, Nadia Nathan, et al.Clinical Endocrinology|April 28, 2011
A novel POU1F1 mutation (p.Thr168IlefsX7) associated with an early and severe form of combined pituitary hormone deficiency: functional analysis and follow-up from infancy to adulthoodYardena Tenenbaum-Rakover, Marie-Laure Sobrier, Serge AmselemPageof 34