Search Results - "Tyson, Weslie"

Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges by Sahoo, Trilochan, Dzidic, Natasa, Strecker, Michelle N., Commander, Sara, Travis, Mary K., Doherty, Charles, Tyson, R. Weslie, Mendoza, Arturo E., Stephenson, Mary, Dise, Craig A., Benito, Carlos W., Ziadie, Mandolin S., Hovanes, Karine

“…Chromosomal microarray analysis (CMA) is currently considered first-tier testing in pediatric care and prenatal diagnosis owing to its high diagnostic…”
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The Intrauterine Growth-Restricted Fetus and Placenta Evaluation by Tyson, R. Weslie, MD, Staat, Barton C., MD

“…Evaluation of the placenta is extremely important in attempting to understand the pathophysiology of intrauterine growth restriction. Only with careful gross…”
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Fulminant epstein‐barr viral hepatitis: Orthotopic liver transplantation and review of the literature by Feranchak, Andrew P., Tyson, R. Weslie, Narkewicz, Michael R., Karrer, Frederick M., Sokol, Ronald J.

“…Acute hepatic failure caused by primary Epstein‐Barr virus (EBV) infection has been reported in the literature in 16 cases, with an overall mortality of 87%…”
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Detection of reovirus RNA in hepatobiliary tissues from patients with extrahepatic biliary atresia and choledochal cysts by Tyler, Kenneth L., Sokol, Ronald J., Oberhaus, Stephanie M., Le, Mysan, Karrer, Frederick M., Narkewicz, Michael R., Tyson, R. Weslie, Murphy, James R., Low, Robert, Brown, William R.

“…Extrahepatic biliary atresia (EHBA) and choledochal cysts (CDC) are important causes of obstructive jaundice in pediatric patients. Viruses in general, and…”
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The role of fetal breathing motions compared with gasping motions in pulmonary airway uptake of intra-amniotic iron dextran by Pollack, Jason A, Moise, Kenneth J, Tyson, Weslie R, Galan, Henry L

“…We hypothesized that normal fetal breathing, not acute asphyxial gasping, results in the movement of iron dextran from the amniotic cavity into the fetal…”
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Astroblastoma: Ultrastructural Observations on a Case of High-Grade Type by Mierau, G W, Tyson, R W, McGavran, L, Parker, N B, Partington, M D

“…An astroblastoma of high-grade type arising in the brain of a 3-year-old child is reported. The first description of the ultrastructural, immunohistochemical,…”
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Adverse Effects of Maternal Enterovirus Infection on the Fetus and Placenta by Palmer, April L., Rotbart, Harley A., Tyson, R. Weslie, Abzug, Mark J.

“…Gestational outcome in a murine model of congenital enterovirus infection was evaluated. Pregnant mice were inoculated intravenously with Theiler's murine…”
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Identification of a new inborn error in bile acid synthesis: mutation of the oxysterol 7alpha-hydroxylase gene causes severe neonatal liver disease by Setchell, K D, Schwarz, M, O'Connell, N C, Lund, E G, Davis, D L, Lathe, R, Thompson, H R, Weslie Tyson, R, Sokol, R J, Russell, D W

“…We describe a metabolic defect in bile acid synthesis involving a deficiency in 7alpha-hydroxylation due to a mutation in the gene for the microsomal oxysterol…”
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Cotyledon and binucleate cell nitric oxide synthase expression in an ovine model of fetal growth restriction by Galan, Henry L, Regnault, Timothy R. H, Le Cras, Timothy D, Tyson, R. Weslie, Anthony, Russell V, Wilkening, Randall B, Abman, Steven H

“…Division of Perinatal Medicine in the Departments of 1  Obstetrics and Gynecology and 2  Pediatrics; 3  Pediatric Heart Lung Center, University of Colorado…”
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Balamuthia mandrillaris meningoencephalitis presenting with acute hydrocephalus by Duke, B J, Tyson, R W, DeBiasi, R, Freeman, J E, Winston, K R

“…The leptomyxid amoeba Balamuthia mandrillaris, previously believed to be a harmless soil-inhabiting organism, is now known to be a rare but consistently lethal…”
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Fibrosing Pancreatitis Associated with Pericholangitis and Cholangitis in a Child by Stephen, Thomas C., Younoszai, M. Kabir, Tyson, R. Weslie, Groff, Diller B.

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Role of electron microscopy in the diagnosis of mitochondrial cytopathies by Mierau, Gary W, Tyson, R Weslie, Freehauf, Cynthia L

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Inefficient transduction of sheep in utero after intra-amniotic injection of retroviral producer cells by Galan, Henry L., Bennett, Michael L., Tyson, R.Weslie, Owens, Geoffrey, Regnault, Timothy R.H., Accurso, Frank, Hobbins, John C., Schaack, Jerome

“…Objective: Our purpose was to test the hypothesis that the intra-amniotic injection of a retroviral vector producer cell line into pregnant sheep will result…”
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Clinical and molecular study in congenital muscular dystrophy with partial laminin α2 (LAMA2) deficiency by Tezak, Zivana, Prandini, Paola, Boscaro, Marco, Marin, Alessandra, Devaney, Joseph, Marino, Michael, Fanin, Marina, Trevisan, Carlo P., Park, Julie, Tyson, Weslie, Finkel, R., Garcia, Carlos, Angelini, Corrado, Hoffman, Eric P., Pegoraro, Elena

“…Complete laminin α2 (LAMA2) deficiency causes approximately half of congenital muscular dystrophy (CMD) cases. Many loss‐of‐function mutations have been…”
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Acute Philadelphia chromosome-positive leukemia in an adolescent boy after liver transplantation by SILLIMAN, Christopher C, TYSON, R. Weslie, QI WEI, KARRER, Frederick G, DAVIES, Stella M, BLAKE, Marilyn, MCGAVRAN, Loris

“…Acute leukemia is an untoward event following immunosuppression for solid organ transplantation and is related to the oncogenic effects of Epstein-Barr viral…”
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Fibrosing Pancreatitis Associated with Pericholangitis and Cholangitis in a Child by Stephen, Thomas C., Younoszai, M. Kabir, Tyson, R. Weslie, Groff, Diller B.

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Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency by Tezak, Zivana, Prandini, Paola, Boscaro, Marco, Marin, Alessandra, Devaney, Joseph, Marino, Michael, Fanin, Marina, Trevisan, Carlo P, Park, Julie, Tyson, Weslie, Finkel, R, Garcia, Carlos, Angelini, Corrado, Hoffman, Eric P, Pegoraro, Elena

“…Complete laminin alpha2 (LAMA2) deficiency causes approximately half of congenital muscular dystrophy (CMD) cases. Many loss-of-function mutations have been…”
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Comprehensive Genetic Analysis of Pregnancy Loss by Chromosomal Microarrays: Outcomes, Benefits, and Challenges by Sahoo, Trilochan, Dzidic, Natasa, Strecker, Michelle N., Commander, Sara, Travis, Mary K., Doherty, Charles, Tyson, R. Weslie, Mendoza, Arturo E., Stephenson, Mary, Dise, Craig A., Benito, Carlos W., Ziadie, Mandolin S., Hovanes, Karine

“…(Abstracted from Genet Med 2017;19(1):83–89) High-resolution chromosomal microarray analysis (CMA) with single-nucleotide polymorphism (SNP)–based arrays is…”
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Clinical and molecular study in congenital muscular dystrophy with partial laminin ?2 (LAMA2) deficiency by Tezak, Zivana, Prandini, Paola, Boscaro, Marco, Marin, Alessandra, Devaney, Joseph, Marino, Michael, Fanin, Marina, Trevisan, Carlo P., Park, Julie, Tyson, Weslie, Finkel, R., Garcia, Carlos, Angelini, Corrado, Hoffman, Eric P., Pegoraro, Elena

“…Complete laminin ±2 (LAMA2) deficiency causes approximately half of congenital muscular dystrophy (CMD) cases. Many loss-of-function mutations have been…”
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Intravascular Ultrasonic Characteristics and Vasoreactivity of the Pulmonary Vasculature in Children With Pulmonary Hypertension by Ivy, D.Dunbar, Neish, Steven R, Knudson, Ole A, Nihill, Michael R, Schaffer, Michael S, Tyson, R.Weslie, Abman, Steven H, Shaffer, Elizabeth M, Valdes-Cruz, Lilliam

“…We sought to describe the morphologic characteristics of pulmonary arteries by intravascular ultrasound (IVUS) in children with and without pulmonary…”
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