Changes in the Diagnosis and Management of Patent Ductus Arteriosus from 2006 to 2015 in United States Neonatal Intensive Care Units
Bixler, G. Michael, MD, Powers, George C., MD, Clark, Reese H., MD, Walker, M. Whit, MD, Tolia, Veeral N., MD
Published in The Journal of pediatrics (01.10.2017)
Published in The Journal of pediatrics (01.10.2017)
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Low Rate of Spontaneous Closure in Premature Infants Discharged with a Patent Ductus Arteriosus: A Multicenter Prospective Study
Tolia, Veeral N., Powers, George C., Kelleher, Amy S., Walker, M. Whit, Herrman, Kristy K., Ahmad, Kaashif A., Buchh, Basharat, Egalka, Matthew C., Hinkes, Michael, Ma, Meiyun, Richards, Moira, Rudine, Anthony C., Sato, Ray Y., Shaffer, Kenneth M., Clark, Reese H.
Published in The Journal of pediatrics (01.01.2022)
Published in The Journal of pediatrics (01.01.2022)
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A patient with a unique frameshift mutation in GPC3, causing Simpson-Golabi-Behmel syndrome, presenting with craniosynostosis, penoscrotal hypospadias, and a large prostatic utricle
Villarreal, Diana D., Villarreal, Humberto, Paez, Ana Maria, Peppas, Dennis, Lynch, Jane, Roeder, Elizabeth, Powers, George C.
Published in American journal of medical genetics. Part A (01.12.2013)
Published in American journal of medical genetics. Part A (01.12.2013)
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A patient with a unique frameshift mutation in GPC3, causing Simpson-Golabi-Behmel syndrome, presenting with craniosynostosis, penoscrotal hypospadias, and a large prostatic utricle-Am J Med Genet Part A 161A: 3121-3125
Villarreal, Diana D., Villarreal, Humberto, Paez, Ana Maria, Peppas, Dennis, Lynch, Jane, Roeder, Elizabeth, Powers, George C.
Published in American journal of medical genetics. Part A (01.07.2014)
Published in American journal of medical genetics. Part A (01.07.2014)
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Intravenous epoprostenol improves oxygenation index in patients with persistent pulmonary hypertension of the newborn refractory to nitric oxide
Ahmad, Kaashif Aqeeb, Banales, Jesse, Henderson, Cody Lance, Ramos, Susanne Erika, Brandt, Katherine Marie, Powers, George Charles
Published in Journal of perinatology (01.09.2018)
Published in Journal of perinatology (01.09.2018)
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LINE‐ and Alu‐containing genomic instability hotspot at 16q24.1 associated with recurrent and nonrecurrent CNV deletions causative for ACDMPV
Szafranski, Przemyslaw, Kośmider, Ewelina, Liu, Qian, Karolak, Justyna A., Currie, Lauren, Parkash, Sandhya, Kahler, Stephen G., Roeder, Elizabeth, Littlejohn, Rebecca O., DeNapoli, Thomas S., Shardonofsky, Felix R., Henderson, Cody, Powers, George, Poisson, Virginie, Bérubé, Denis, Oligny, Luc, Michaud, Jacques L., Janssens, Sandra, Coen, Kris, Dorpe, Jo, Dheedene, Annelies, Harting, Matthew T., Weaver, Matthew D., Khan, Amir M., Tatevian, Nina, Wambach, Jennifer, Gibbs, Kathleen A., Popek, Edwina, Gambin, Anna, Stankiewicz, Paweł
Published in Human mutation (01.12.2018)
Published in Human mutation (01.12.2018)
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Journal Article
LINE-and Alu-containing genomic instability hotspotat 16q24.1 associated with recurrent and nonrecurrent CNV deletions causative for ACDMPV
Szafranski, Przemyslaw, Kośmider, Ewelina, Liu, Qian, Karolak, Justyna A., Currie, Lauren, Parkash, Sandhya, Kahler, Stephen G., Roeder, Elizabeth, Littlejohn, Rebecca O., DeNapoli, Thomas S., Shardonofsky, Felix R., Henderson, Cody, Powers, George, Poisson, Virginie, Bérubé, Denis, Oligny, Luc, Michaud, Jacques L., Janssens, Sandra, De Coen, Kris, Van Dorpe, Jo, Dheedene, Annelies, Harting, Matthew T., Weaver, Matthew D., Khan, Amir M., Tatevian, Nina, Wambach, Jennifer, Gibbs, Kathleen A., Popek, Edwina, Gambin, Anna, Stankiewicz, Paweł
Published in Human mutation (22.08.2018)
Published in Human mutation (22.08.2018)
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