Search Results - "Pyle, Meredith E"

Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease by Bean, Christopher J., Boulet, Sheree L., Ellingsen, Dorothy, Pyle, Meredith E., Barron-Casella, Emily A., Casella, James F., Payne, Amanda B., Driggers, Jennifer, Trau, Heidi A., Yang, Genyan, Jones, Kimberly, Ofori-Acquah, Solomon F., Hooper, W. Craig, DeBaun, Michael R.

“…Sickle cell disease is a common hemolytic disorder with a broad range of complications, including vaso-occlusive episodes, acute chest syndrome (ACS), pain,…”
Get full text

Magnetic resonance angiography-defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose-6-phosphate dehydrogenase mutation in children with sickle cell anaemia by Thangarajh, Mathula, Yang, Genyan, Fuchs, Dana, Ponisio, Maria R., McKinstry, Robert C., Jaju, Alok, Noetzel, Michael J., Casella, James F., Barron-Casella, Emily, Hooper, W. Craig, Boulet, Sheree L., Bean, Christopher J., Pyle, Meredith E., Payne, Amanda B., Driggers, Jennifer, Trau, Heidi A., Vendt, Bruce A., Rodeghier, Mark, DeBaun, Michael R.

“…Summary Silent cerebral infarct (SCI) is the most commonly recognized cause of neurological injury in sickle cell anaemia (SCA). We tested the hypothesis that…”
Get full text

Whole blood gene expression profiles distinguish clinical phenotypes of venous thromboembolism by Lewis, Deborah A, Suchindran, Sunil, Beckman, Michele G, Hooper, W. Craig, Grant, Althea M, Heit, John A, Manco-Johnson, Marilyn, Moll, Stephan, Philipp, Claire S, Kenney, Kristy, De Staercke, Christine, Pyle, Meredith E, Chi, Jen-Tsan, Ortel, Thomas L

“…Abstract Introduction Recurrent venous thromboembolism (VTE) occurs infrequently following a provoked event but occurs in up to 30% of individuals following an…”
Get full text

Acute chest syndrome is associated with single nucleotide polymorphism‐defined beta globin cluster haplotype in children with sickle cell anaemia by Bean, Christopher J., Boulet, Sheree L., Yang, Genyan, Payne, Amanda B., Ghaji, Nafisa, Pyle, Meredith E., Hooper, W. Craig, Bhatnagar, Pallav, Keefer, Jeffrey, Barron‐Casella, Emily A., Casella, James F., DeBaun, Michael R.

“…Summary Genetic diversity at the human β‐globin locus has been implicated as a modifier of sickle cell anaemia (SCA) severity. However, haplotypes defined by…”
Get full text