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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 Research|February 17, 2012
An intronic ABCA3 mutation that is responsible for respiratory diseaseAmit Agrawal, Aaron Hamvas, F Sessions Cole, et al.
Neonatology|June 19, 2007
Genetic disorders of surfactant proteinsAaron Hamvas, F Sessions Cole, Lawrence M Nogee
Pediatric Clinics of North America|October 10, 2006
Defects in surfactant synthesis: clinical implicationsF Sessions Cole, Lawrence M Nogee, Aaron Hamvas
American Journal of Respiratory and Critical Care Medicine|May 30, 2014
Genotype-phenotype correlations for infants and children with ABCA3 deficiencyJennifer A Wambach, Alicia M Casey, Martha P Fishman, et al.
Pediatrics|November 21, 2012
Single ABCA3 mutations increase risk for neonatal respiratory distress syndromeJennifer A Wambach, Daniel J Wegner, Kelcey Depass, et al.
The Journal of Pediatrics|March 4, 2016
Genetic Factors Contribute to Risk for Neonatal Respiratory Distress Syndrome among Moderately Preterm, Late Preterm, and Term InfantsCarol L Shen, Qunyuan Zhang, Julia Meyer Hudson, et al.
The Journal of Pediatrics|October 3, 2006
Long-term outcomes after infant lung transplantation for surfactant protein B deficiency related to other causes of respiratory failureLisanne M Palomar, Lawrence M Nogee, Stuart C Sweet, 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.
Journal of the Endocrine Society|November 19, 2020
Digenic Variants in the FGF21 Signaling Pathway Associated with Severe Insulin Resistance and PseudoacromegalyStephen I Stone, Daniel J Wegner, Jennifer A Wambach, et al.
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