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Lawrence M Nogee

Showing results (21-30 of 83) with videos related to

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Seminars in Perinatology|December 5, 2006
ABCA3 deficiency: neonatal respiratory failure and interstitial lung diseaseJanine E Bullard, Susan E Wert, Lawrence M Nogee
Clinics in Perinatology|June 11, 2026
Evaluation and Management of Genetic Respiratory Disorders Presenting as Hypoxemic Respiratory Failure in the Newborn InfantJennifer A Wambach, F Sessions Cole, Lawrence M Nogee
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 18, 2009
Genetic disorders of surfactant dysfunctionSusan E Wert, Jeffrey A Whitsett, Lawrence M Nogee
American Journal of Respiratory Cell and Molecular Biology|January 25, 2022
First Steps toward Personalized Therapies for ABCA3 DeficiencyJennifer A Wambach, Lawrence M Nogee, F Sessions Cole
Pediatric Pulmonology|July 3, 2013
Variable clinical outcome of ABCA3 deficiency in two siblingsSurendran Thavagnanam, Ernest Cutz, David Manson, et al.
The Journal of Biological Chemistry|October 4, 2003
Expression of a human surfactant protein C mutation associated with interstitial lung disease disrupts lung development in transgenic miceJames P Bridges, Susan E Wert, Lawrence M Nogee, et al.
American Journal of Respiratory and Critical Care Medicine|June 25, 2005
ABCA3 mutations associated with pediatric interstitial lung diseaseJanine E Bullard, Susan E Wert, Jeffrey A Whitsett, et al.
Chest|June 22, 2013
A mutation in TTF1/NKX2.1 is associated with familial neuroendocrine cell hyperplasia of infancyLisa R Young, Gail H Deutsch, Ronald E Bokulic, et al.
Pediatric Pulmonology|July 1, 2016
A novel surfactant protein C gene mutation associated with progressive respiratory failure in infancyMelissa Kaori Silva Litao, Don Hayes, Saurabh Chiwane, et al.
Pediatrics|April 6, 2011
Pulmonary nodules in a newborn with ATP-binding cassette transporter A3 (ABCA3) mutationsDerek A Uchida, Susan E Wert, Lawrence M Nogee, et al.
Pageof 9

Showing results (21-30 of 83) with videos related to

Sort By:
Pageof 9
Seminars in Perinatology|December 5, 2006
ABCA3 deficiency: neonatal respiratory failure and interstitial lung diseaseJanine E Bullard, Susan E Wert, Lawrence M Nogee
Clinics in Perinatology|June 11, 2026
Evaluation and Management of Genetic Respiratory Disorders Presenting as Hypoxemic Respiratory Failure in the Newborn InfantJennifer A Wambach, F Sessions Cole, Lawrence M Nogee
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 18, 2009
Genetic disorders of surfactant dysfunctionSusan E Wert, Jeffrey A Whitsett, Lawrence M Nogee
American Journal of Respiratory Cell and Molecular Biology|January 25, 2022
First Steps toward Personalized Therapies for ABCA3 DeficiencyJennifer A Wambach, Lawrence M Nogee, F Sessions Cole
Pediatric Pulmonology|July 3, 2013
Variable clinical outcome of ABCA3 deficiency in two siblingsSurendran Thavagnanam, Ernest Cutz, David Manson, et al.
The Journal of Biological Chemistry|October 4, 2003
Expression of a human surfactant protein C mutation associated with interstitial lung disease disrupts lung development in transgenic miceJames P Bridges, Susan E Wert, Lawrence M Nogee, et al.
American Journal of Respiratory and Critical Care Medicine|June 25, 2005
ABCA3 mutations associated with pediatric interstitial lung diseaseJanine E Bullard, Susan E Wert, Jeffrey A Whitsett, et al.
Chest|June 22, 2013
A mutation in TTF1/NKX2.1 is associated with familial neuroendocrine cell hyperplasia of infancyLisa R Young, Gail H Deutsch, Ronald E Bokulic, et al.
Pediatric Pulmonology|July 1, 2016
A novel surfactant protein C gene mutation associated with progressive respiratory failure in infancyMelissa Kaori Silva Litao, Don Hayes, Saurabh Chiwane, et al.
Pediatrics|April 6, 2011
Pulmonary nodules in a newborn with ATP-binding cassette transporter A3 (ABCA3) mutationsDerek A Uchida, Susan E Wert, Lawrence M Nogee, et al.
Pageof 9