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Journal of Clinical Medicine|June 2, 2021
Left Ventricle Phenotyping Utilizing Tissue Doppler Imaging in Premature Infants with Varying Severity of Bronchopulmonary DysplasiaEunice Torres, Philip T Levy, Afif El-Khuffash, et al.BMC Medical Genetics|October 10, 2013
Rare recessive loss-of-function methionyl-tRNA synthetase mutations presenting as a multi-organ phenotypeEline van Meel, Daniel J Wegner, Paul Cliften, et al.Bone|March 28, 2019
Phenotype and response to growth hormone therapy in siblings with B4GALT7 deficiencyCarla Sandler-Wilson, Jennifer A Wambach, Bess A Marshall, et al.Journal of Molecular Biology|April 28, 2004
The N-terminal propeptide of lung surfactant protein C is necessary for biosynthesis and prevents unfolding of a metastable alpha-helixJing Li, Waltteri Hosia, Aaron Hamvas, et al.The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|December 27, 2018
Addressing medically underserved populations through maternal-fetal transport: a geographic analysisJoshua I Rosenbloom, D Michael Nelson, Scott Saunders, et al.Cold Spring Harbor Molecular Case Studies|June 14, 2020
Neonatal respiratory failure due to novel compound heterozygous mutations in the ABCA3 lipid transporterZoltán N Oltvai, Eric A Smith, Katie Wiens, et al.Journal of Lipid Research|May 29, 2009
Metabolic precursors of surfactant disaturated-phosphatidylcholine in preterms with respiratory distressPaola E Cogo, Carlo Ori, Manuela Simonato, et al.JAMA Network Open|August 27, 2021
Cardiac Performance in the First Year of Age Among Preterm Infants Fed Maternal Breast MilkAfif El-Khuffash, Adam J Lewandowski, Amish Jain, et al.Neonatology|December 26, 2016
Thoracoabdominal Asynchrony Is Not Associated with Oxyhemoglobin Saturation in Recovering Premature InfantsColleen Brennan, Lara Ulm, Samuel Julian, et al.Molecular Genetics and Metabolism|May 12, 2020
The common K333Q polymorphism in long-chain acyl-CoA dehydrogenase (LCAD) reduces enzyme stability and functionMegan E Beck, Yuxun Zhang, Sivakama S Bharathi, et al.Pageof 22