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Respiratory Research
|
April 16, 2014
A large kindred of pulmonary fibrosis associated with a novel ABCA3 gene variant
Ilaria Campo, Michele Zorzetto, Francesca Mariani, et al.
Pediatric Research
|
September 17, 2015
Surfactant proteins in pediatric interstitial lung disease
Matthias Griese, Elke Lorenz, Meike Hengst, et al.
BMC Pulmonary Medicine
|
August 13, 2015
GATA2 deficiency in children and adults with severe pulmonary alveolar proteinosis and hematologic disorders
Matthias Griese, Ralf Zarbock, Ulrich Costabel, et al.
American Journal of Human Genetics
|
April 28, 2015
Biallelic Mutations of Methionyl-tRNA Synthetase Cause a Specific Type of Pulmonary Alveolar Proteinosis Prevalent on Réunion Island
Alice Hadchouel, Thomas Wieland, Matthias Griese, et al.
Molecular Medicine (Cambridge, Mass.)
|
March 2, 2016
Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3
Thomas Wittmann, Sabrina Frixel, Stefanie Höppner, et al.
The European Respiratory Journal
|
February 7, 2015
Genotype alone does not predict the clinical course of SFTPC deficiency in paediatric patients
Carolin Kröner, Simone Reu, Veronika Teusch, et al.
Thorax
|
August 13, 2016
Lung disease caused by <i>ABCA3</i> mutations
Carolin Kröner, Thomas Wittmann, Simone Reu, et al.
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Search research articles
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Showing results (21-30 of 27) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 27 results.
Respiratory Research
|
April 16, 2014
A large kindred of pulmonary fibrosis associated with a novel ABCA3 gene variant
Ilaria Campo, Michele Zorzetto, Francesca Mariani, et al.
Pediatric Research
|
September 17, 2015
Surfactant proteins in pediatric interstitial lung disease
Matthias Griese, Elke Lorenz, Meike Hengst, et al.
BMC Pulmonary Medicine
|
August 13, 2015
GATA2 deficiency in children and adults with severe pulmonary alveolar proteinosis and hematologic disorders
Matthias Griese, Ralf Zarbock, Ulrich Costabel, et al.
American Journal of Human Genetics
|
April 28, 2015
Biallelic Mutations of Methionyl-tRNA Synthetase Cause a Specific Type of Pulmonary Alveolar Proteinosis Prevalent on Réunion Island
Alice Hadchouel, Thomas Wieland, Matthias Griese, et al.
Molecular Medicine (Cambridge, Mass.)
|
March 2, 2016
Increased Risk of Interstitial Lung Disease in Children with a Single R288K Variant of ABCA3
Thomas Wittmann, Sabrina Frixel, Stefanie Höppner, et al.
The European Respiratory Journal
|
February 7, 2015
Genotype alone does not predict the clinical course of SFTPC deficiency in paediatric patients
Carolin Kröner, Simone Reu, Veronika Teusch, et al.
Thorax
|
August 13, 2016
Lung disease caused by <i>ABCA3</i> mutations
Carolin Kröner, Thomas Wittmann, Simone Reu, et al.
Page
of 3