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Lawrence M Nogee

Showing results (61-70 of 83) with videos related to

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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.
Orphanet Journal of Rare Diseases|July 27, 2017
Childhood interstitial lung diseases in immunocompetent children in Australia and New Zealand: a decade's experienceVishal Saddi, Sean Beggs, Bruce Bennetts, 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.
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.
Pediatric Pulmonology|July 11, 2012
Frontiers in pulmonary hypertension in infants and children with bronchopulmonary dysplasiaJoseph M Collaco, Lewis H Romer, Bridget D Stuart, 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.
American Journal of Respiratory and Critical Care Medicine|July 13, 2010
Hereditary pulmonary alveolar proteinosis: pathogenesis, presentation, diagnosis, and therapyTakuji Suzuki, Takuro Sakagami, Lisa R Young, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Accurate assignment of disease liability to genetic variants using only population dataJoseph M Collaco, Karen S Raraigh, Joshua Betz, et al.
Pageof 9

Showing results (61-70 of 83) with videos related to

Sort By:
Pageof 9
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.
Orphanet Journal of Rare Diseases|July 27, 2017
Childhood interstitial lung diseases in immunocompetent children in Australia and New Zealand: a decade's experienceVishal Saddi, Sean Beggs, Bruce Bennetts, 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.
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.
Pediatric Pulmonology|July 11, 2012
Frontiers in pulmonary hypertension in infants and children with bronchopulmonary dysplasiaJoseph M Collaco, Lewis H Romer, Bridget D Stuart, 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.
American Journal of Respiratory and Critical Care Medicine|July 13, 2010
Hereditary pulmonary alveolar proteinosis: pathogenesis, presentation, diagnosis, and therapyTakuji Suzuki, Takuro Sakagami, Lisa R Young, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Accurate assignment of disease liability to genetic variants using only population dataJoseph M Collaco, Karen S Raraigh, Joshua Betz, et al.
Pageof 9