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American Journal of Physiology. Lung Cellular and Molecular Physiology|October 17, 2023
Loss of prolyl hydroxylase 1 and 2 in SM22α-expressing cells prevents Hypoxia-Induced pulmonary hypertensionElizabeth A Barnes, Reiji Ito, Xibing Che, et al.Pulmonary Circulation|October 31, 2019
Diminished right ventricular function at diagnosis of pulmonary hypertension is associated with mortality in bronchopulmonary dysplasiaGabriel Altit, Shazia Bhombal, Jeffrey Feinstein, et al.The Review of Scientific Instruments|August 7, 2025
An inflatable "finger-lock" for stabilizing nailfold capillary videos and modulating blood flow velocitiesMarcus L Forst, Gabriela Rincon, Juliette H Levy, et al.Journal of Perinatology : Official Journal of the California Perinatal Association|January 9, 2019
Death or resolution: the "natural history" of pulmonary hypertension in bronchopulmonary dysplasiaGabriel Altit, Shazia Bhombal, Rachel K Hopper, et al.American Journal of Physiology. Lung Cellular and Molecular Physiology|October 22, 2002
Pulmonary vascular K+ channel expression and vasoreactivity in a model of congenital heart diseaseDavid N Cornfield, Ernesto R Resnik, Jean M Herron, et al.American Journal of Physiology. Lung Cellular and Molecular Physiology|December 13, 2006
Chronic intrauterine pulmonary hypertension increases capacitative calcium entry in fetal pulmonary artery smooth muscle cellsErnesto R Resnik, Maggie Keck, David J Sukovich, et al.Current Opinion in Pulmonary Medicine|May 20, 2026
Recent advances in the clinical management of end-stage pediatric pulmonary hypertensionOscar van der Have, Rachel K Hopper, Rebecca J Kameny, et al.Pulmonary Circulation|May 4, 2022
A case of acquired von Willebrand disease in severe pediatric pulmonary hypertension contributing to bleeding following reverse Potts shuntRachel T Sullivan, Clara Lo, Elisabeth Martin, et al.Chest|March 7, 2009
Quantitative analysis of longitudinal response to aerosolized granulocyte-macrophage colony-stimulating factor in two adolescents with autoimmune pulmonary alveolar proteinosisTerry E Robinson, Bruce C Trapnell, Michael L Goris, et al.American Journal of Medical Genetics. Part A|February 24, 2015
Neonatal pulmonary arterial hypertension and Noonan syndrome: two fatal cases with a specific RAF1 mutationRachel K Hopper, Jeffrey A Feinstein, Melanie A Manning, et al.Pageof 14