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Diagnostics (Basel, Switzerland)
|
December 23, 2022
Genetics in Idiopathic Pulmonary Fibrosis: A Clinical Perspective
Spyros A Papiris, Caroline Kannengiesser, Raphael Borie, et al.
Pediatric Pulmonology
|
December 31, 2015
Eosinophilic pneumonias in children: A review of the epidemiology, diagnosis, and treatment
Lisa 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 adulthood
Effrosyni D Manali, Marie Legendre, Nadia Nathan, et al.
Breathe (Sheffield, England)
|
May 14, 2025
An update on diagnosis and treatments of childhood interstitial lung diseases
Honorata 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 disease
Yohan 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(®) cohort
Jessica Taytard, Nadia Nathan, Jacques de Blic, et al.
Medical Education Online
|
June 27, 2024
Clues for improvement of research in objective structured clinical examination
Jean Philippe Foy, Laure Serresse, Maxens Decavèle, et al.
Pediatric Pulmonology
|
January 2, 2024
Lung biopsies in infants and children in critical care situation
Yaël Levy, Lauren Bitton, Chiara Sileo, et al.
Orphanet Journal of Rare Diseases
|
February 22, 2014
Idiopathic eosinophilic pneumonia in children: the French experience
Lisa 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 deficiency
Mathilde Le Brun, Nadia Nathan, Camille Louvrier, et al.
Page
of 13
Search research articles
Search
Showing results (71-80 of 124) with videos related to
Sort By:
Page
of 13
Diagnostics (Basel, Switzerland)
|
December 23, 2022
Genetics in Idiopathic Pulmonary Fibrosis: A Clinical Perspective
Spyros A Papiris, Caroline Kannengiesser, Raphael Borie, et al.
Pediatric Pulmonology
|
December 31, 2015
Eosinophilic pneumonias in children: A review of the epidemiology, diagnosis, and treatment
Lisa 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 adulthood
Effrosyni D Manali, Marie Legendre, Nadia Nathan, et al.
Breathe (Sheffield, England)
|
May 14, 2025
An update on diagnosis and treatments of childhood interstitial lung diseases
Honorata 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 disease
Yohan 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(®) cohort
Jessica Taytard, Nadia Nathan, Jacques de Blic, et al.
Medical Education Online
|
June 27, 2024
Clues for improvement of research in objective structured clinical examination
Jean Philippe Foy, Laure Serresse, Maxens Decavèle, et al.
Pediatric Pulmonology
|
January 2, 2024
Lung biopsies in infants and children in critical care situation
Yaël Levy, Lauren Bitton, Chiara Sileo, et al.
Orphanet Journal of Rare Diseases
|
February 22, 2014
Idiopathic eosinophilic pneumonia in children: the French experience
Lisa 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 deficiency
Mathilde Le Brun, Nadia Nathan, Camille Louvrier, et al.
Page
of 13