Search Results - "Beecroft, Taylor"

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    Genetic Testing for Supravalvar Aortic Stenosis: What to Do When It Is Not Williams Syndrome by Stephens, Sara B, Novy, Tyler, Spurzem, Gabrielle N, Jacob, Benjamin, Beecroft, Taylor, Soludczyk, Emily, Kozel, Beth A, Weigand, Justin, Morris, Shaine A

    Published in Journal of the American Heart Association (16-04-2024)
    “…We aimed to describe the frequency and yield of genetic testing in supravalvar aortic stenosis (SVAS) following negative evaluation for…”
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    Journal Article
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    Extracellular microRNAs in blood differentiate between ischaemic and haemorrhagic stroke subtypes by Kalani, M. Yashar S., Alsop, Eric, Meechoovet, Bessie, Beecroft, Taylor, Agrawal, Komal, Whitsett, Timothy G., Huentelman, Matthew J., Spetzler, Robert F., Nakaji, Peter, Kim, Seungchan, Van Keuren-Jensen, Kendall

    Published in Journal of extracellular vesicles (01-01-2020)
    “…Rapid identification of patients suffering from cerebral ischaemia, while excluding intracerebral haemorrhage, can assist with patient triage and expand…”
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    microRNA changes in liver tissue associated with fibrosis progression in patients with hepatitis C by Van Keuren-Jensen, Kendall R., Malenica, Ivana, Courtright, Amanda L., Ghaffari, Layla T., Starr, Alex P., Metpally, Raghu P., Beecroft, Taylor A., Carlson, Elizabeth W.J., Kiefer, Jeffrey A., Pockros, Paul J., Rakela, Jorge

    Published in Liver international (01-03-2016)
    “…Background & Aims Accumulating evidence indicates that microRNAs play a role in a number of disease processes including the pathogenesis of liver fibrosis in…”
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    Journal Article
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    Abstract 12192: Arterial Tortuosity Syndrome: A Longitudinal Assessment Of Cardiovascular Features by Salamat, Bita, Taylor, Andrea, Stephens, Sara, Beecroft, Taylor, Weigand, Justin, Jacob, Ben, Morris, Shaine A

    Published in Circulation (New York, N.Y.) (16-11-2021)
    “…IntroductionArterial tortuosity syndrome (ATS) is an ultra-rare arteriopathy caused by pathogenic biallelic variants in SLC2A10 leading to tortuosity,…”
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    Evaluating perinatal and neonatal outcomes among children with vascular Ehlers–Danlos syndrome by Stephens, Sara B., Russo, Melissa, Shalhub, Sherene, Beecroft, Taylor, Weigand, Justin, Milewicz, Dianna M., Morris, Shaine A.

    Published in Genetics in medicine (01-10-2022)
    “…Birth outcomes data for patients with vascular Ehlers–Danlos syndrome (VEDS) are limited. Patients with a pathogenic or likely pathogenic COL3A1 variant were…”
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    Journal Article
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    Evaluating Variation in the Cardiac Management of Children with Hereditary Thoracic Aortic Disease in the United States by Weyland, Cassie N., Salciccioli, Katherine B., Beecroft, Taylor, Soludczyk, Emily N., Morris, Shaine A.

    Published in Pediatric cardiology (01-01-2024)
    “…Hereditary thoracic aortic diseases (HTAD) such as Marfan syndrome (MFS), Loeys–Dietz syndrome (LDS), and vascular Ehlers–Danlos syndrome (VEDS) frequently…”
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    Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age by Freud, Lindsay R., Galloway, Stephanie, Crowley, T. Blaine, Moldenhauer, Julie, Swillen, Ann, Breckpot, Jeroen, Borrell, Antoni, Vora, Neeta L., Cuneo, Bettina, Hoffman, Hilary, Gilbert, Lisa, Nowakowska, Beata, Geremek, Maciej, Kutkowska-Kaźmierczak, Anna, Vermeesch, Joris R., Devriendt, Koen, Busa, Tiffany, Sigaudy, Sabine, Vigneswaran, Trisha, Simpson, John M., Dungan, Jeffrey, Gotteiner, Nina, Gloning, Karl-Philipp, Digilio, Maria Cristina, Unolt, Marta, Putotto, Carolina, Marino, Bruno, Repetto, Gabriela, Fadic, Magdalena, Garcia-Minaur, Sixto, Achón Buil, Ana, Thomas, Mary Ann, Fruitman, Deborah, Beecroft, Taylor, Hui, Pui Wah, Oskarsdottir, Solveig, Bradshaw, Rachael, Criebaum, Amanda, Norton, Mary E., Lee, Tiffany, Geiger, Miwa, Dunnington, Leslie, Isaac, Jacqueline, Wilkins-Haug, Louise, Hunter, Lindsey, Izzi, Claudia, Toscano, Marika, Ghi, Tullio, McGlynn, Julie, Romana Grati, Francesca, Emanuel, Beverly S., Gaiser, Kimberly, Gaynor, J. William, Goldmuntz, Elizabeth, McGinn, Daniel E., Schindewolf, Erica, Tran, Oanh, Zackai, Elaine H., Yan, Qi, Bassett, Anne S., Wapner, Ronald, McDonald-McGinn, Donna M.

    “…The 22q11.2 deletion syndrome is the most common microdeletion syndrome and is frequently associated with congenital heart disease. Prenatal diagnosis of…”
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    micro RNA changes in liver tissue associated with fibrosis progression in patients with hepatitis C by Van Keuren‐Jensen, Kendall R., Malenica, Ivana, Courtright, Amanda L., Ghaffari, Layla T., Starr, Alex P., Metpally, Raghu P., Beecroft, Taylor A., Carlson, Elizabeth W.J., Kiefer, Jeffrey A., Pockros, Paul J., Rakela, Jorge

    Published in Liver international (01-03-2016)
    “…Abstract Background & Aims Accumulating evidence indicates that micro RNA s play a role in a number of disease processes including the pathogenesis of liver…”
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    Journal Article
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