Imaging Findings in Pediatric COVID-19: A Review of Current Literature

por Fick, Tyler A., Cua, Clifford L., Lee, Simon
Publicado 2022

Thrombosis Prevention and Anticoagulation Management in the Pediatric Patient with Congenital Heart Disease

por Abdelghani, Eman, Cua, Clifford L., Giver, Jean, Rodriguez, Vilmarie
Publicado 2021

Utility of Follow-Up Echocardiograms in Uncomplicated Surgical Secundum Atrial Septal Defect Closures: Preliminary Analysis

por Gupta, Ritika, Mah, May Ling, Bowman, Jessica, Cua, Clifford L.
Publicado 2023

Caring for a Child with Hypoplastic Left Heart Syndrome: Parent and Medical Perspective

por Nicholas, Benjamin, Nicholas, Christina, Allen, Robin L., Cua, Clifford L.
Publicado 2021

Usefulness of Postnatal Echocardiograms in Patients with Omphaloceles Who Previously Had a Normal Fetal Echocardiogram

por Clark, Michael, Aldrink, Jennifer H., Richards, Bernadette, Corbitt, Rebecca, Stiver, Corey, Cua, Clifford L.
Publicado 2021

Ortner’s Syndrome in an Infant With Congenital Heart Disease

por Murillo-Deluquez, Marcelino, McKee, Christopher, Collazos-Noriega, Misael, Cua, Clifford L., Tobias, Joseph D.
Publicado 2022

Utility of Follow-Up Echocardiograms in Uncomplicated PDA Device Closures Performed After Infancy

por Reo, Rachel, Van Pelt, Erin, Lovelace, Casey, Eshelman, Anne, Beckman, Brian, Chisolm, Joanne, Boe, Brian, Backes, Carl, Cua, Clifford L.
Publicado 2022

Utility of Follow-Up Echocardiograms in Uncomplicated PDA Device Closures Performed During Infancy

por Van Pelt, Erin, Reo, Rachel, Lovelace, Casey, Eshelman, Anne, Beckman, Brian, Chisolm, Joanne, Boe, Brian, Backes, Carl, Cua, Clifford L.
Publicado 2022

Early prediction of spontaneous Patent Ductus Arteriosus (PDA) closure and PDA-associated outcomes: a prospective cohort investigation

por Slaughter, Jonathan L., Cua, Clifford L., Notestine, Jennifer L., Rivera, Brian K., Marzec, Laura, Hade, Erinn M., Maitre, Nathalie L., Klebanoff, Mark A., Ilgenfritz, Megan, Le, Vi T., Lewandowski, Dennis J., Backes, Carl H.
Publicado 2019

Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects

por Rambo-Martin, Benjamin L., Mulle, Jennifer G., Cutler, David J., Bean, Lora J. H., Rosser, Tracie C., Dooley, Kenneth J., Cua, Clifford, Capone, George, Maslen, Cheryl L., Reeves, Roger H., Sherman, Stephanie L., Zwick, Michael E.
Publicado 2017

Contribution of Copy Number Variation to Down Syndrome-associated Atrioventricular Septal Defects

por Ramachandran, Dhanya, Mulle, Jennifer G., Locke, Adam E., Bean, Lora J.H., Rosser, Tracie C., Bose, Promita, Dooley, Kenneth J., Cua, Clifford L., Capone, George T., Reeves, Roger H., Maslen, Cheryl L., Cutler, David J., Sherman, Stephanie L., Zwick, Michael E.
Publicado 2014

Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects

por Ramachandran, Dhanya, Zeng, Zhen, Locke, Adam E., Mulle, Jennifer G., Bean, Lora J.H., Rosser, Tracie C., Dooley, Kenneth J., Cua, Clifford L., Capone, George T., Reeves, Roger H., Maslen, Cheryl L., Cutler, David J., Feingold, Eleanor, Sherman, Stephanie L., Zwick, Michael E.
Publicado 2015

Cardiovascular Complications of Down Syndrome: Scoping Review and Expert Consensus

por Dimopoulos, Konstantinos, Constantine, Andrew, Clift, Paul, Condliffe, Robin, Moledina, Shahin, Jansen, Katrijn, Inuzuka, Ryo, Veldtman, Gruschen R., Cua, Clifford L., Tay, Edgar Lik Wui, Opotowsky, Alexander R., Giannakoulas, George, Alonso-Gonzalez, Rafael, Cordina, Rachael, Capone, George, Namuyonga, Judith, Scott, Charmaine H., D’Alto, Michele, Gamero, Francisco J., Chicoine, Brian, Gu, Hong, Limsuwan, Alisa, Majekodunmi, Tosin, Budts, Werner, Coghlan, Gerry, Broberg, Craig S.
Publicado 2023

Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome

por Trevino, Cristina E., Holleman, Aaron M., Corbitt, Holly, Maslen, Cheryl L., Rosser, Tracie C., Cutler, David J., Johnston, H. Richard, Rambo-Martin, Benjamin L., Oberoi, Jai, Dooley, Kenneth J., Capone, George T., Reeves, Roger H., Cordell, Heather J., Keavney, Bernard D., Agopian, A.J., Goldmuntz, Elizabeth, Gruber, Peter J., O’Brien, James E., Bittel, Douglas C., Wadhwa, Lalita, Cua, Clifford L., Moskowitz, Ivan P., Mulle, Jennifer G., Epstein, Michael P., Sherman, Stephanie L., Zwick, Michael E.
Publicado 2020

Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome

por Trevino, Cristina E., Holleman, Aaron M., Corbitt, Holly, Maslen, Cheryl L., Rosser, Tracie C., Cutler, David J., Johnston, H. Richard, Rambo-Martin, Benjamin L., Oberoi, Jai, Dooley, Kenneth J., Capone, George T., Reeves, Roger H., Cordell, Heather J., Keavney, Bernard D., Agopian, A. J., Goldmuntz, Elizabeth, Gruber, Peter J., O’Brien, James E., Bittel, Douglas C., Wadhwa, Lalita, Cua, Clifford L., Moskowitz, Ivan P., Mulle, Jennifer G., Epstein, Michael P., Sherman, Stephanie L., Zwick, Michael E.
Publicado 2021