Search research articles
Contact Us
Filters
Showing results (31-40 of 114) with videos related to
Page
of 12
Sort By:
Pediatric Pulmonology
|
June 25, 2010
Diffuse chondroid malformation of the lung: cases series of a hitherto undescribed congenital lung disease
Philippe Reix, Stéphanie Wanin, Fréderique Dijoud, et al.
Chest
|
October 6, 2011
BAL fluid surfactant protein C level is related to parenchymal lung disease in children with sarcoidosis
Loïc Guillot, Florence Flamein, Guillaume Thouvenin, et al.
Respiratory Research
|
April 12, 2005
Deficiency in type 1 insulin-like growth factor receptor in mice protects against oxygen-induced lung injury
Karmene Ahamed, Ralph Epaud, Martin Holzenberger, et al.
Pediatric Pulmonology
|
September 2, 2021
Impact of COVID-19 social distancing on viral infection in France: A delayed outbreak of RSV
Céline Delestrain, Kostas Danis, Isabelle Hau, et al.
American Journal of Respiratory Cell and Molecular Biology
|
November 1, 2022
Instability of Mature ABCA3 Protein: Toward a New Classification of ABCA3 Mutations?
Marion Onnée, Bénédicte Duriez, Stéphanie Simon, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
November 14, 2019
Interstitial lung disease reveals 48,XXYY syndrome in a child
Marion Gros, Abdel Aissat, Stephanie Perez-Martin, et al.
Respiratory Medicine and Research
|
June 6, 2024
FREnch National Cohort of neuroendocrine cell Hyperplasia of Infancy (FRENCHI): Long-term consequences and risk factors of low body mass index
Jean-Christophe Dubus, Morgane Dervaux, Caroline Thumerelle, et al.
Pediatric Pulmonology
|
December 5, 2015
Effectiveness of palivizumab in children with childhood interstitial lung disease: The French experience
David Drummond, Caroline Thumerelle, Philippe Reix, et al.
European Journal of Human Genetics : EJHG
|
March 16, 2017
Deciphering the mechanism of Q145H SFTPC mutation unmasks a splicing defect and explains the severity of the phenotype
Céline Delestrain, Stéphanie Simon, Abdel Aissat, et al.
BMC Pediatrics
|
June 8, 2014
Clinical predictors of radiographic abnormalities among infants with bronchiolitis in a paediatric emergency department
Emmanuelle Ecochard-Dugelay, Muriel Beliah, Francis Perreaux, et al.
Page
of 12
Search research articles
Search
Showing results (31-40 of 114) with videos related to
Sort By:
Page
of 12
Pediatric Pulmonology
|
June 25, 2010
Diffuse chondroid malformation of the lung: cases series of a hitherto undescribed congenital lung disease
Philippe Reix, Stéphanie Wanin, Fréderique Dijoud, et al.
Chest
|
October 6, 2011
BAL fluid surfactant protein C level is related to parenchymal lung disease in children with sarcoidosis
Loïc Guillot, Florence Flamein, Guillaume Thouvenin, et al.
Respiratory Research
|
April 12, 2005
Deficiency in type 1 insulin-like growth factor receptor in mice protects against oxygen-induced lung injury
Karmene Ahamed, Ralph Epaud, Martin Holzenberger, et al.
Pediatric Pulmonology
|
September 2, 2021
Impact of COVID-19 social distancing on viral infection in France: A delayed outbreak of RSV
Céline Delestrain, Kostas Danis, Isabelle Hau, et al.
American Journal of Respiratory Cell and Molecular Biology
|
November 1, 2022
Instability of Mature ABCA3 Protein: Toward a New Classification of ABCA3 Mutations?
Marion Onnée, Bénédicte Duriez, Stéphanie Simon, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
November 14, 2019
Interstitial lung disease reveals 48,XXYY syndrome in a child
Marion Gros, Abdel Aissat, Stephanie Perez-Martin, et al.
Respiratory Medicine and Research
|
June 6, 2024
FREnch National Cohort of neuroendocrine cell Hyperplasia of Infancy (FRENCHI): Long-term consequences and risk factors of low body mass index
Jean-Christophe Dubus, Morgane Dervaux, Caroline Thumerelle, et al.
Pediatric Pulmonology
|
December 5, 2015
Effectiveness of palivizumab in children with childhood interstitial lung disease: The French experience
David Drummond, Caroline Thumerelle, Philippe Reix, et al.
European Journal of Human Genetics : EJHG
|
March 16, 2017
Deciphering the mechanism of Q145H SFTPC mutation unmasks a splicing defect and explains the severity of the phenotype
Céline Delestrain, Stéphanie Simon, Abdel Aissat, et al.
BMC Pediatrics
|
June 8, 2014
Clinical predictors of radiographic abnormalities among infants with bronchiolitis in a paediatric emergency department
Emmanuelle Ecochard-Dugelay, Muriel Beliah, Francis Perreaux, et al.
Page
of 12