Gastrocystoplasty

Yazar: Carr, Michael C., Mitchell, Michael E.
Yayımlandı ScientificWorldJournal (2004)

Effect of endomyocardial biopsy on levels of donor-specific cell-free DNA

Yazar: Zangwill, Steven D., Stamm, Karl D., Hidestrand, Mats, Tomita-Mitchell, Aoy, Mitchell, Michael E.
Yayımlandı J Heart Lung Transplant (2019)

Cardiac Arrest Secondary to Traumatic Aortopulmonary Window During Transcatheter Pulmonary Valve Implantation in Supported Ross

Yazar: Chongthammakun, Vasutakarn, Mitchell, Michael E., Gudausky, Todd M., Bartz, Peter J., Foerster, Susan R.
Yayımlandı JACC Case Rep (2019)

Use of Metformin in Pulmonary Vein Stenosis after TAPVR Repair

Yazar: Kirkpatrick, Edward C., Mitchell, Michael E., Thilly, William G., Cava, Joseph, Tomita-Mitchell, Aoy, Gostjeva, Elena V.
Yayımlandı Glob Pediatr Health (2020)

Comparison of Patch Materials for Pulmonary Artery Reconstruction

Yazar: Ebert, Nicholas, McGinnis, Michael, Johnson, William, Kuhn, Evelyn M., Mitchell, Michael E., Tweddell, James S., Woods, Ronald K.
Yayımlandı Semin Thorac Cardiovasc Surg (2020)

Effect of 22q11.2 deletion on bleeding and transfusion utilization in children with congenital heart disease undergoing cardiac surgery

Yazar: Brenner, Michelle K., Clarke, Shanelle, Mahnke, Donna K., Simpson, Pippa, Bercovitz, Rachel S., Tomita-Mitchell, Aoy, Mitchell, Michael E., Newman, Debra K.
Yayımlandı Pediatr Res (2015)

Non-Invasive Prenatal Detection of Trisomy 21 Using Tandem Single Nucleotide Polymorphisms

Yazar: Ghanta, Sujana, Mitchell, Michael E., Ames, Mary, Hidestrand, Mats, Simpson, Pippa, Goetsch, Mary, Thilly, William G., Struble, Craig A., Tomita-Mitchell, Aoy
Baskı/Yayın Bilgisi 2010

Early changes in cell‐free DNA levels in newly transplanted heart transplant patients

Yazar: Zangwill, Steven D., Kindel, Steven J., Ragalie, William S., North, Paula E., Pollow, Alyssa, Hidestrand, Mats, Tomita‐Mitchell, Aoy, Stamm, Karl D., Mitchell, Michael E.
Yayımlandı Pediatr Transplant (2019)

Fibroblast growth factor-10 signals development of von Brunn's nests in the exstrophic bladder

Yazar: Eastman, Rocky, Leaf, Elizabeth M., Zhang, Dianzhong, True, Lawrence D., Sweet, Robert M., Seidel, Kristy, Siebert, Joseph R., Grady, Richard, Mitchell, Michael E., Bassuk, James A.
Baskı/Yayın Bilgisi 2010

Multiplexed quantitative real-time PCR to detect 22q11.2 deletion in patients with congenital heart disease

Yazar: Tomita-Mitchell, Aoy, Mahnke, Donna K., Larson, Joshua M., Ghanta, Sujana, Feng, Ying, Simpson, Pippa M., Broeckel, Ulrich, Duffy, Kelly, Tweddell, James S., Grossman, William J., Routes, John M., Mitchell, Michael E.
Baskı/Yayın Bilgisi 2010

Highly Sensitive Non-Invasive Cardiac Transplant Rejection Monitoring Using Targeted Quantification of Donor Specific Cell Free DNA

Yazar: Hidestrand, Mats, Tomita-Mitchell, Aoy, Hidestrand, Pip M, Oliphant, Arnold, Goetsch, Mary, Stamm, Karl, Liang, Huan-Ling, Castleberry, Chesney, Benson, D. Woodrow, Stendahl, Gail, Simpson, Pippa M, Berger, Stuart, Tweddell, James S, Zangwill, Steven, Mitchell, Michael E
Yayımlandı J Am Coll Cardiol (2013)

Cell-free DNA donor fraction analysis in pediatric and adult heart transplant patients by multiplexed allele-specific quantitative PCR: Validation of a rapid and highly sensitive c...

Yazar: North, Paula E., Ziegler, Emily, Mahnke, Donna K., Stamm, Karl D., Thomm, Angela, Daft, Paul, Goetsch, Mary, Liang, Huan ling, Baker, Maria Angeles, Vepraskas, Adam, Rosenau, Chris, Dasgupta, Mahua, Simpson, Pippa, Mitchell, Michael E., Tomita-Mitchell, Aoy
Yayımlandı PLoS One (2020)

Contractility of Induced Pluripotent Stem Cell-Cardiomyocytes With an MYH6 Head Domain Variant Associated With Hypoplastic Left Heart Syndrome

Yazar: Kim, Min-Su, Fleres, Brandon, Lovett, Jerrell, Anfinson, Melissa, Samudrala, Sai Suma K., Kelly, Lauren J., Teigen, Laura E., Cavanaugh, Matthew, Marquez, Maribel, Geurts, Aron M., Lough, John W., Mitchell, Michael E., Fitts, Robert H., Tomita-Mitchell, Aoy
Yayımlandı Front Cell Dev Biol (2020)

Renin-Angiotensin-Aldosterone Genotype Influences Ventricular Remodeling in Infants with Single Ventricle

Yazar: Mital, Seema, Chung, Wendy K., Colan, Steven D., Sleeper, Lynn A., Manlhiot, Cedric, Arrington, Cammon B., Cnota, James F., Graham, Eric M., Mitchell, Michael E., Goldmuntz, Elizabeth, Li, Jennifer S., Levine, Jami C., Lee, Teresa M., Margossian, Renee, Hsu, Daphne T.
Baskı/Yayın Bilgisi 2011

Human gene copy number spectra analysis in congenital heart malformations

Yazar: Tomita-Mitchell, Aoy, Mahnke, Donna K., Struble, Craig A., Tuffnell, Maureen E., Stamm, Karl D., Hidestrand, Mats, Harris, Susan E., Goetsch, Mary A., Simpson, Pippa M., Bick, David P., Broeckel, Ulrich, Pelech, Andrew N., Tweddell, James S., Mitchell, Michael E.
Baskı/Yayın Bilgisi 2012

Impact of MYH6 variants in hypoplastic left heart syndrome

Yazar: Tomita-Mitchell, Aoy, Stamm, Karl D., Mahnke, Donna K., Kim, Min-Su, Hidestrand, Pip M., Liang, Huan Ling, Goetsch, Mary A., Hidestrand, Mats, Simpson, Pippa, Pelech, Andrew N., Tweddell, James S., Benson, D. Woodrow, Lough, John W., Mitchell, Michael E.
Yayımlandı Physiol Genomics (2016)

Human genotyping and an experimental model reveal NPR-C as a possible contributor to morbidity in coarctation of the aorta

Yazar: LaDisa, John F., Tomita-Mitchell, Aoy, Stamm, Karl, Bazan, Kathleen, Mahnke, Donna K., Goetsch, Mary A., Wegter, Brandon J., Gerringer, Jesse W., Repp, Kathryn, Palygin, Oleg, Zietara, Adrian P., Krolikowski, Mary M., Eddinger, Thomas J., Alli, Abdel A., Mitchell, Michael E.
Yayımlandı Physiol Genomics (2019)

Novel KLHL26 variant associated with a familial case of Ebstein’s anomaly and left ventricular noncompaction

Yazar: Samudrala, Sai Suma K., North, Lauren M., Stamm, Karl D., Earing, Michael G., Frommelt, Michele A., Willes, Richard, Tripathi, Swarnendu, Dsouza, Nikita R., Zimmermann, Michael T., Mahnke, Donna K., Liang, Huan Ling, Lund, Michael, Lin, Chien‐Wei, Geddes, Gabrielle C., Mitchell, Michael E., Tomita‐Mitchell, Aoy
Yayımlandı Mol Genet Genomic Med (2020)

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3

Yazar: Guo, Tingwei, Repetto, Gabriela M., McDonald McGinn, Donna M., Chung, Jonathan H., Nomaru, Hiroko, Campbell, Christopher L., Blonska, Anna, Bassett, Anne S., Chow, Eva W.C., Mlynarski, Elisabeth E., Swillen, Ann, Vermeesch, Joris, Devriendt, Koen, Gothelf, Doron, Carmel, Miri, Michaelovsky, Elena, Schneider, Maude, Eliez, Stephan, Antonarakis, Stylianos E., Coleman, Karlene, Tomita-Mitchell, Aoy, Mitchell, Michael E., Digilio, M. Cristina, Dallapiccola, Bruno, Marino, Bruno, Philip, Nicole, Busa, Tiffany, Kushan-Wells, Leila, Bearden, Carrie E., Piotrowicz, Małgorzata, Hawuła, Wanda, Roberts, Amy E., Tassone, Flora, Simon, Tony J., van Duin, Esther D.A., van Amelsvoort, Thérèse A., Kates, Wendy R., Zackai, Elaine, Johnston, H. Richard, Cutler, David J., Agopian, A.J., Goldmuntz, Elizabeth, Mitchell, Laura E., Wang, Tao, Emanuel, Beverly S., Morrow, Bernice E.
Yayımlandı Circ Cardiovasc Genet (2017)