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Nadia Nathan

Showing results (91-100 of 124) with videos related to

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Respiratory Medicine|May 12, 2026
Malnutrition in childhood interstitial lung diseases is associated with reduced lung function and greater disease severity: insights from the chILD-EU registryTugba Ramasli Gursoy, Nagehan Emiralioglu, Matthias Griese, et al.
BMC Medical Genomics|March 8, 2018
Whole exome sequencing in three families segregating a pediatric case of sarcoidosisAlain Calender, Pierre Antoine Rollat Farnier, Adrien Buisson, et al.
Respiratory Medicine|July 23, 2017
Heterogeneity of lung disease associated with NK2 homeobox 1 mutationsElodie Nattes, Stephanie Lejeune, Ania Carsin, et al.
European Journal of Pediatrics|November 30, 2022
Long-term evolution of neuroendocrine cell hyperplasia of infancy: the FRENCHI findingsMorgane Dervaux, Caroline Thumerelle, Candice Fabre, et al.
European Journal of Pediatrics|June 9, 2022
French national cohort of neuroendocrine cell hyperplasia of infancy (FRENCHI) study: diagnosis and initial managementCandice Fabre, Caroline Thumerelle, Morgane Dervaux, et al.
The European Respiratory Journal|September 18, 2025
De novo <b><i>SRRM2</i></b> variants in neuroendocrine cell hyperplasia of infancy and persistent tachypnea of infancyCamille Louvrier, Yohan Soreze, Julie Mesinele, et al.
Orphanet Journal of Rare Diseases|December 5, 2019
Pilot experience of multidisciplinary team discussion dedicated to inherited pulmonary fibrosisRaphael Borie, Caroline Kannengiesser, Laurent Gouya, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 23, 2025
Younger Age and Viral Triggers Were Associated With Post-Infectious Bronchiolitis Obliterans in French ChildrenJulie Mazenq, Marine Crebassa, Alice Hadchouel, et al.
Orphanet Journal of Rare Diseases|April 22, 2018
Pulmonary hemosiderosis in children with Down syndrome: a national experienceAurelia Alimi, Jessica Taytard, Rola Abou Taam, et al.
Human Molecular Genetics|January 22, 2016
Germline SFTPA1 mutation in familial idiopathic interstitial pneumonia and lung cancerNadia Nathan, Violaine Giraud, Clément Picard, et al.
Pageof 13

Showing results (91-100 of 124) with videos related to

Sort By:
Pageof 13
Respiratory Medicine|May 12, 2026
Malnutrition in childhood interstitial lung diseases is associated with reduced lung function and greater disease severity: insights from the chILD-EU registryTugba Ramasli Gursoy, Nagehan Emiralioglu, Matthias Griese, et al.
BMC Medical Genomics|March 8, 2018
Whole exome sequencing in three families segregating a pediatric case of sarcoidosisAlain Calender, Pierre Antoine Rollat Farnier, Adrien Buisson, et al.
Respiratory Medicine|July 23, 2017
Heterogeneity of lung disease associated with NK2 homeobox 1 mutationsElodie Nattes, Stephanie Lejeune, Ania Carsin, et al.
European Journal of Pediatrics|November 30, 2022
Long-term evolution of neuroendocrine cell hyperplasia of infancy: the FRENCHI findingsMorgane Dervaux, Caroline Thumerelle, Candice Fabre, et al.
European Journal of Pediatrics|June 9, 2022
French national cohort of neuroendocrine cell hyperplasia of infancy (FRENCHI) study: diagnosis and initial managementCandice Fabre, Caroline Thumerelle, Morgane Dervaux, et al.
The European Respiratory Journal|September 18, 2025
De novo <b><i>SRRM2</i></b> variants in neuroendocrine cell hyperplasia of infancy and persistent tachypnea of infancyCamille Louvrier, Yohan Soreze, Julie Mesinele, et al.
Orphanet Journal of Rare Diseases|December 5, 2019
Pilot experience of multidisciplinary team discussion dedicated to inherited pulmonary fibrosisRaphael Borie, Caroline Kannengiesser, Laurent Gouya, et al.
Acta Paediatrica (Oslo, Norway : 1992)|June 23, 2025
Younger Age and Viral Triggers Were Associated With Post-Infectious Bronchiolitis Obliterans in French ChildrenJulie Mazenq, Marine Crebassa, Alice Hadchouel, et al.
Orphanet Journal of Rare Diseases|April 22, 2018
Pulmonary hemosiderosis in children with Down syndrome: a national experienceAurelia Alimi, Jessica Taytard, Rola Abou Taam, et al.
Human Molecular Genetics|January 22, 2016
Germline SFTPA1 mutation in familial idiopathic interstitial pneumonia and lung cancerNadia Nathan, Violaine Giraud, Clément Picard, et al.
Pageof 13