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Aaron Hamvas

Showing results (81-90 of 113) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992)|April 13, 2007
Novel mutations in the gene encoding ATP binding cassette protein member A3 (ABCA3) resulting in fatal neonatal lung diseaseOla D Saugstad, Thor Willy Ruud Hansen, Arild Rønnestad, et al.
American Journal of Respiratory Cell and Molecular Biology|December 6, 2003
Progressive lung disease and surfactant dysfunction with a deletion in surfactant protein C geneAaron Hamvas, Lawrence M Nogee, Frances V White, et al.
Pediatric Research|March 5, 2008
Population and disease-based prevalence of the common mutations associated with surfactant deficiencyTami H Garmany, Jennifer A Wambach, Hillary B Heins, et al.
American Journal of Respiratory and Critical Care Medicine|August 3, 2013
An official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancyGeoffrey Kurland, Robin R Deterding, James S Hagood, et al.
Clinical Epigenetics|April 10, 2019
Novel parent-of-origin-specific differentially methylated loci on chromosome 16Katharina V Schulze, Przemyslaw Szafranski, Harry Lesmana, et al.
Nature Methods|March 3, 2009
Quantification of rare allelic variants from pooled genomic DNATodd E Druley, Francesco L M Vallania, Daniel J Wegner, et al.
The Journal of Pediatrics|August 4, 2009
Inherited surfactant deficiency caused by uniparental disomy of rare mutations in the surfactant protein-B and ATP binding cassette, subfamily a, member 3 genesAaron Hamvas, Lawrence M Nogee, Daniel J Wegner, et al.
Pediatric Pulmonology|April 3, 2008
Recombination as a mechanism for sporadic mutation in the surfactant protein-C geneAmy D McBee, Daniel J Wegner, Christopher S Carlson, et al.
BMC Pediatrics|April 18, 2015
Prematurity and respiratory outcomes program (PROP): study protocol of a prospective multicenter study of respiratory outcomes of preterm infants in the United StatesGloria S Pryhuber, Nathalie L Maitre, Roberta A Ballard, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 7, 2012
High-resolution structure of a BRICHOS domain and its implications for anti-amyloid chaperone activity on lung surfactant protein CHanna Willander, Glareh Askarieh, Michael Landreh, et al.
Pageof 12

Showing results (81-90 of 113) with videos related to

Sort By:
Pageof 12
Acta Paediatrica (Oslo, Norway : 1992)|April 13, 2007
Novel mutations in the gene encoding ATP binding cassette protein member A3 (ABCA3) resulting in fatal neonatal lung diseaseOla D Saugstad, Thor Willy Ruud Hansen, Arild Rønnestad, et al.
American Journal of Respiratory Cell and Molecular Biology|December 6, 2003
Progressive lung disease and surfactant dysfunction with a deletion in surfactant protein C geneAaron Hamvas, Lawrence M Nogee, Frances V White, et al.
Pediatric Research|March 5, 2008
Population and disease-based prevalence of the common mutations associated with surfactant deficiencyTami H Garmany, Jennifer A Wambach, Hillary B Heins, et al.
American Journal of Respiratory and Critical Care Medicine|August 3, 2013
An official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancyGeoffrey Kurland, Robin R Deterding, James S Hagood, et al.
Clinical Epigenetics|April 10, 2019
Novel parent-of-origin-specific differentially methylated loci on chromosome 16Katharina V Schulze, Przemyslaw Szafranski, Harry Lesmana, et al.
Nature Methods|March 3, 2009
Quantification of rare allelic variants from pooled genomic DNATodd E Druley, Francesco L M Vallania, Daniel J Wegner, et al.
The Journal of Pediatrics|August 4, 2009
Inherited surfactant deficiency caused by uniparental disomy of rare mutations in the surfactant protein-B and ATP binding cassette, subfamily a, member 3 genesAaron Hamvas, Lawrence M Nogee, Daniel J Wegner, et al.
Pediatric Pulmonology|April 3, 2008
Recombination as a mechanism for sporadic mutation in the surfactant protein-C geneAmy D McBee, Daniel J Wegner, Christopher S Carlson, et al.
BMC Pediatrics|April 18, 2015
Prematurity and respiratory outcomes program (PROP): study protocol of a prospective multicenter study of respiratory outcomes of preterm infants in the United StatesGloria S Pryhuber, Nathalie L Maitre, Roberta A Ballard, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 7, 2012
High-resolution structure of a BRICHOS domain and its implications for anti-amyloid chaperone activity on lung surfactant protein CHanna Willander, Glareh Askarieh, Michael Landreh, et al.
Pageof 12