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Ralf Zarbock

Showing results (21-30 of 27) with videos related to

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Respiratory Research|April 16, 2014
A large kindred of pulmonary fibrosis associated with a novel ABCA3 gene variantIlaria Campo, Michele Zorzetto, Francesca Mariani, et al.
Pediatric Research|September 17, 2015
Surfactant proteins in pediatric interstitial lung diseaseMatthias 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 disordersMatthias 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 IslandAlice 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 ABCA3Thomas 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 patientsCarolin Kröner, Simone Reu, Veronika Teusch, et al.
Thorax|August 13, 2016
Lung disease caused by <i>ABCA3</i> mutationsCarolin Kröner, Thomas Wittmann, Simone Reu, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
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 variantIlaria Campo, Michele Zorzetto, Francesca Mariani, et al.
Pediatric Research|September 17, 2015
Surfactant proteins in pediatric interstitial lung diseaseMatthias 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 disordersMatthias 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 IslandAlice 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 ABCA3Thomas 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 patientsCarolin Kröner, Simone Reu, Veronika Teusch, et al.
Thorax|August 13, 2016
Lung disease caused by <i>ABCA3</i> mutationsCarolin Kröner, Thomas Wittmann, Simone Reu, et al.
Pageof 3