Search Results - "Norton, M.E."

Agenesis of the Corpus Callosum: An MR Imaging Analysis of Associated Abnormalities in the Fetus by Tang, P.H, Bartha, A.I, Norton, M.E, Barkovich, A.J, Sherr, E.H, Glenn, O.A

“…Anomalies associated with callosal agenesis (ACC) found postnatally have been well documented. However, to our knowledge, no detailed MR imaging analysis of…”
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Observed Rate of Down Syndrome in Twin Pregnancies by Sparks, T.N, Norton, M.E, Flessel, M, Goldman, S, Currier, R.J

“…(Obstet Gynecol. 2016;128(5):1127–1133)The risk of Down syndrome in twin pregnancies is not well established, although some studies suggest that it may be…”
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Society for Maternal-Fetal Medicine (SMFM) Clinical Guideline #8: The Fetus at Risk for Anemia—Diagnosis and Management by Mari, G, Norton, M.E, Stone, J, Berghella, V, Sciscione, A.C, Tate, D, Schenone, M.H

“…(Am J Obstet Gynecol. 2015;212(6):697–710)Fetal anemia is a life-threatening condition that is typically caused by red cell alloimmunization or parvovirus…”
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Treatment for Mild Chronic Hypertension during Pregnancy by Tita, Alan T., Szychowski, Jeff M., Boggess, Kim, Dugoff, Lorraine, Sibai, Baha, Lawrence, Kirsten, Hughes, Brenna L., Bell, Joseph, Aagaard, Kjersti, Edwards, Rodney K., Gibson, Kelly, Haas, David M., Plante, Lauren, Metz, Torri, Casey, Brian, Esplin, Sean, Longo, Sherri, Hoffman, Matthew, Saade, George R., Hoppe, Kara K., Foroutan, Janelle, Tuuli, Methodius, Owens, Michelle Y., Simhan, Hyagriv N., Frey, Heather, Rosen, Todd, Palatnik, Anna, Baker, Susan, August, Phyllis, Reddy, Uma M., Kinzler, Wendy, Su, Emily, Krishna, Iris, Nguyen, Nicki, Norton, Mary E., Skupski, Daniel, El-Sayed, Yasser Y., Ogunyemi, Dotum, Galis, Zorina S., Harper, Lorie, Ambalavanan, Namasivayam, Geller, Nancy L., Oparil, Suzanne, Cutter, Gary R., Andrews, William W.

“…Pregnant women with mild chronic hypertension were randomly assigned to receive medication targeting a normal blood pressure (<140/90 mm Hg) or to receive no…”
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Fetal hydrops and the Incremental yield of Next‐generation sequencing over standard prenatal Diagnostic testing (FIND) study: prospective cohort study and meta‐analysis by Mone, F., Eberhardt, R. Y., Hurles, M. E., Mcmullan, D. J., Maher, E. R., Lord, J., Chitty, L. S., Dempsey, E., Homfray, T., Giordano, J. L., Wapner, R. J., Sun, L., Sparks, T. N., Norton, M. E., Kilby, M. D.

“…ABSTRACT Objective To determine the incremental yield of exome sequencing (ES) over chromosomal microarray analysis (CMA) or karyotyping in prenatally…”
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VP33.09: Exome sequencing versus gene panels for non‐immune hydrops fetalis by Sparks, T., Van Ziffle, J., Devine, P., Lianoglou, B., Norton, M.E.

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VP08.01: RASopathies and their prenatal presentations with non‐immune hydrops spectrum by Sparks, T., Lianoglou, B., Jelin, A., Gilmore, K., Downum, S., Vora, N., Norton, M.E.

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OC05.08: Prenatal screening and testing for 45,X: lessons learned from 18,299 cfDNA results from the SMART study by Martin, K., Norton, M.E., Clifton, R., Jacobsson, B., Haeri, S., Egbert, M., Malone, F.D., Wapner, R.J., Roman, A., Khalil, A., Faro, R., Madankumar, R., Edwards, L., Strong, N., Silver, R., Vohra, N., Hyett, J., Billings, P., Kao, C., Dar, P.

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OC05.04: Prenatal screening for 22q11.2DS: does it change patient care? by Martin, K., Norton, M.E., Jacobsson, B., Haeri, S., Egbert, M., Malone, F.D., Wapner, R.J., Roman, A., Khalil, A., Faro, R., Madankumar, R., Edwards, L., Strong, N., Silver, R., Vohra, N., Hyett, J., Billings, P., Kao, C., Dar, P., MacPherson, C.

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Care Levels for Fetal Therapy Centers by Baschat, A.A., Blackwell, S.B., Chatterjee, D., Cummings, J.J., Emery, S.P., Hirose, S., Hollier, L.M., Johnson, A., Kilpatrick, S.J., Luks, F.I., Menard, M.K., McCullough, L.B., Moldenhauer, J.S., Moon-Grady, A.J., Mychaliska, G.B., Narvey, M., Norton, M.E., Rollins, M.D., Skarsgard, E.D., Tsao, K., Warner, B.B., Wilpers, A., Ryan, G.

“…( Obstet Gynecol . 2022;139:1027–1042. doi: 10.1097/AOG.0000000000004793) Fetal therapy carries both benefits and extensive risks for the fetus and pregnant…”
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Congenital heart defects in a large, unselected cohort of monochorionic twins by Pettit, K E, Merchant, M, Machin, G A, Tacy, T A, Norton, M E

“…Objective: To determine the prevalence of congenital heart defects (CHDs) in a large, unselected cohort of monochorionic (MC) twins. Study Design: We completed…”
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Transdisciplinary translational science and the case of preterm birth by Stevenson, D K, Shaw, G M, Wise, P H, Norton, M E, Druzin, M L, Valantine, H A, McFarland, D A

“…Medical researchers have called for new forms of translational science that can solve complex medical problems. Mainstream science has made complementary calls…”
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Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis by Sparks, T.N., Lianoglou, B.R., Adami, R.R., Pluym, I.D., Holliman, K., Duffy, K., Downum, S.L., Patel, S., Faubel, A., Boe, N.M., Field, N.T., Murphy, A., Laurent, L.C., Jolley, J., Uy, C., Slavotinek, A.M., Devine, P., Hodoglugil, U., Van Ziffle, J., Sanders, S.J., MacKenzie, T.C., Norton, M.E.

“…(N Engl J Med. 2020;383:1746–1756) Nonimmune hydrops fetalis (NIHF) is a severe disorder associated with a high risk of stillbirth, preterm birth, neonatal…”
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Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation by EGGERDING, F. A, SCHONBERG, S. A, CHEHAB, F. F, NORTON, M. E, COX, V. A, EPSTEIN, C. J

“…Uniparental isodisomy resulting from the simultaneous presence of isochromosomes of the p and q arms of a chromosome and absence of a normal homologue is an…”
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