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Annick Clement

Showing results (1-10 of 100) with videos related to

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Current Opinion in Pulmonary Medicine|March 9, 2018
Genetic causes and clinical management of pediatric interstitial lung diseasesNadia Nathan, Keren Borensztajn, Annick Clement
Expert Review of Molecular Diagnostics|July 5, 2008
Hyperinflammation in airways of cystic fibrosis patients: what's new?Jacky Jacquot, Olivier Tabary, Annick Clement
Paediatric Respiratory Reviews|May 12, 2004
The pathogenesis of interstitial lung diseases in childrenAnnick Clement, Alexandra Henrion-Caude, Brigitte Fauroux
BMJ Case Reports|July 2, 2013
Diffuse parenchymal lung disease caused by surfactant deficiency: dramatic improvement by azithromycinGuillaume Thouvenin, Nadia Nathan, Ralph Epaud, et al.
Orphanet Journal of Rare Diseases|April 8, 2025
The RaDiCo information system for rare disease cohortsPaul Landais, Sonia Gueguen, Annick Clement, et al.
Expert Review of Respiratory Medicine|October 23, 2018
Chronic interstitial lung diseases in children: diagnosis approachesNadia Nathan, Laura Berdah, Keren Borensztajn, et al.
Paediatric Respiratory Reviews|June 2, 2015
Biomarkers in Interstitial lung diseasesNadia Nathan, Harriet Corvol, Serge Amselem, et al.
BMJ Case Reports|November 13, 2012
A rare CFTR intronic mutation related to a mild CF disease in a 12-year-old girlNadia Nathan, Emmanuelle Girodon, Annick Clement, et al.
The International Journal of Biochemistry & Cell Biology|April 25, 2008
Airway epithelial cell inflammatory signalling in cystic fibrosisJacky Jacquot, Olivier Tabary, Philippe Le Rouzic, et al.
Orphanet Journal of Rare Diseases|August 24, 2010
Interstitial lung diseases in childrenAnnick Clement, Nadia Nathan, Ralph Epaud, et al.
Pageof 10

Showing results (1-10 of 100) with videos related to

Sort By:
Pageof 10
Current Opinion in Pulmonary Medicine|March 9, 2018
Genetic causes and clinical management of pediatric interstitial lung diseasesNadia Nathan, Keren Borensztajn, Annick Clement
Expert Review of Molecular Diagnostics|July 5, 2008
Hyperinflammation in airways of cystic fibrosis patients: what's new?Jacky Jacquot, Olivier Tabary, Annick Clement
Paediatric Respiratory Reviews|May 12, 2004
The pathogenesis of interstitial lung diseases in childrenAnnick Clement, Alexandra Henrion-Caude, Brigitte Fauroux
BMJ Case Reports|July 2, 2013
Diffuse parenchymal lung disease caused by surfactant deficiency: dramatic improvement by azithromycinGuillaume Thouvenin, Nadia Nathan, Ralph Epaud, et al.
Orphanet Journal of Rare Diseases|April 8, 2025
The RaDiCo information system for rare disease cohortsPaul Landais, Sonia Gueguen, Annick Clement, et al.
Expert Review of Respiratory Medicine|October 23, 2018
Chronic interstitial lung diseases in children: diagnosis approachesNadia Nathan, Laura Berdah, Keren Borensztajn, et al.
Paediatric Respiratory Reviews|June 2, 2015
Biomarkers in Interstitial lung diseasesNadia Nathan, Harriet Corvol, Serge Amselem, et al.
BMJ Case Reports|November 13, 2012
A rare CFTR intronic mutation related to a mild CF disease in a 12-year-old girlNadia Nathan, Emmanuelle Girodon, Annick Clement, et al.
The International Journal of Biochemistry & Cell Biology|April 25, 2008
Airway epithelial cell inflammatory signalling in cystic fibrosisJacky Jacquot, Olivier Tabary, Philippe Le Rouzic, et al.
Orphanet Journal of Rare Diseases|August 24, 2010
Interstitial lung diseases in childrenAnnick Clement, Nadia Nathan, Ralph Epaud, et al.
Pageof 10