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Nadia Nathan

Showing results (71-80 of 124) with videos related to

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Diagnostics (Basel, Switzerland)|December 23, 2022
Genetics in Idiopathic Pulmonary Fibrosis: A Clinical PerspectiveSpyros A Papiris, Caroline Kannengiesser, Raphael Borie, et al.
Pediatric Pulmonology|December 31, 2015
Eosinophilic pneumonias in children: A review of the epidemiology, diagnosis, and treatmentLisa Giovannini-Chami, Sibylle Blanc, Alice Hadchouel, et al.
ERJ Open Research|July 31, 2019
Bi-allelic missense <i>ABCA3</i> mutations in a patient with childhood ILD who reached adulthoodEffrosyni D Manali, Marie Legendre, Nadia Nathan, et al.
Breathe (Sheffield, England)|May 14, 2025
An update on diagnosis and treatments of childhood interstitial lung diseasesHonorata Marczak, Katarzyna Krenke, Matthias Griese, et al.
Plos One|December 19, 2025
Deciphering the pathogenicity of three NKX2-1 variants in ultra-severe forms of childhood interstitial lung diseaseYohan David Soreze, Tifenn Desroziers-Louedec, Aurore Carré, et al.
Orphanet Journal of Rare Diseases|October 16, 2013
New insights into pediatric idiopathic pulmonary hemosiderosis: the French RespiRare(®) cohortJessica Taytard, Nadia Nathan, Jacques de Blic, et al.
Medical Education Online|June 27, 2024
Clues for improvement of research in objective structured clinical examinationJean Philippe Foy, Laure Serresse, Maxens Decavèle, et al.
Pediatric Pulmonology|January 2, 2024
Lung biopsies in infants and children in critical care situationYaël Levy, Lauren Bitton, Chiara Sileo, et al.
Orphanet Journal of Rare Diseases|February 22, 2014
Idiopathic eosinophilic pneumonia in children: the French experienceLisa Giovannini-Chami, Alice Hadchouel, Nadia Nathan, et al.
ERJ Open Research|March 5, 2025
Efficacy and safety of CFTR modulators in patients with interstitial lung disease caused by ABCA3 transporter deficiencyMathilde Le Brun, Nadia Nathan, Camille Louvrier, et al.
Pageof 13

Showing results (71-80 of 124) with videos related to

Sort By:
Pageof 13
Diagnostics (Basel, Switzerland)|December 23, 2022
Genetics in Idiopathic Pulmonary Fibrosis: A Clinical PerspectiveSpyros A Papiris, Caroline Kannengiesser, Raphael Borie, et al.
Pediatric Pulmonology|December 31, 2015
Eosinophilic pneumonias in children: A review of the epidemiology, diagnosis, and treatmentLisa Giovannini-Chami, Sibylle Blanc, Alice Hadchouel, et al.
ERJ Open Research|July 31, 2019
Bi-allelic missense <i>ABCA3</i> mutations in a patient with childhood ILD who reached adulthoodEffrosyni D Manali, Marie Legendre, Nadia Nathan, et al.
Breathe (Sheffield, England)|May 14, 2025
An update on diagnosis and treatments of childhood interstitial lung diseasesHonorata Marczak, Katarzyna Krenke, Matthias Griese, et al.
Plos One|December 19, 2025
Deciphering the pathogenicity of three NKX2-1 variants in ultra-severe forms of childhood interstitial lung diseaseYohan David Soreze, Tifenn Desroziers-Louedec, Aurore Carré, et al.
Orphanet Journal of Rare Diseases|October 16, 2013
New insights into pediatric idiopathic pulmonary hemosiderosis: the French RespiRare(®) cohortJessica Taytard, Nadia Nathan, Jacques de Blic, et al.
Medical Education Online|June 27, 2024
Clues for improvement of research in objective structured clinical examinationJean Philippe Foy, Laure Serresse, Maxens Decavèle, et al.
Pediatric Pulmonology|January 2, 2024
Lung biopsies in infants and children in critical care situationYaël Levy, Lauren Bitton, Chiara Sileo, et al.
Orphanet Journal of Rare Diseases|February 22, 2014
Idiopathic eosinophilic pneumonia in children: the French experienceLisa Giovannini-Chami, Alice Hadchouel, Nadia Nathan, et al.
ERJ Open Research|March 5, 2025
Efficacy and safety of CFTR modulators in patients with interstitial lung disease caused by ABCA3 transporter deficiencyMathilde Le Brun, Nadia Nathan, Camille Louvrier, et al.
Pageof 13