Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 24


Reagent substitution in the chromogenic Bethesda assay for factor VIII inhibitors.

Payne AB, Miller CH, Ellingsen D, Driggers J, Boylan B, Bean CJ.

Haemophilia. 2019 Jul 29. doi: 10.1111/hae.13827. [Epub ahead of print] No abstract available.


HLA-DRB1-factor VIII binding is a risk factor for inhibitor development in nonsevere hemophilia: a case-control study.

Kempton CL, Payne AB.

Blood Adv. 2018 Jul 24;2(14):1750-1755. doi: 10.1182/bloodadvances.2018019323.


Exercise capacity and clinical outcomes in adults followed in the Cooperative Study of Sickle Cell Disease (CSSCD).

Badawy SM, Payne AB, Rodeghier MJ, Liem RI.

Eur J Haematol. 2018 Oct;101(4):532-541. doi: 10.1111/ejh.13140. Epub 2018 Aug 31.


Sexual Assault Nurse Examiner Forensic Examinations for Immigrant Victims: A Case Study.

Payne A.

J Forensic Nurs. 2018 Apr/Jun;14(2):112-116. doi: 10.1097/JFN.0000000000000192.


Low level of the plasma sphingolipid, glucosylceramide, is associated with thrombotic diseases.

Deguchi H, Navarro S, Payne AB, Elias DJ, Dowling NF, Austin HD, España F, Medina P, Hooper WC, Griffin JH.

Res Pract Thromb Haemost. 2017 Jul;1(1):33-40. doi: 10.1002/rth2.12018. Epub 2017 Jun 23.


Low forced expiratory volume is associated with earlier death in sickle cell anemia.

Kassim AA, Payne AB, Rodeghier M, Macklin EA, Strunk RC, DeBaun MR.

Blood. 2015 Sep 24;126(13):1544-50. doi: 10.1182/blood-2015-05-644435. Epub 2015 Aug 10.


Characteristics of hemophilia patients with factor VIII inhibitors detected by prospective screening.

Miller CH, Rice AS, Boylan B, Payne AB, Kelly FM, Escobar MA, Gill J, Leissinger C, Soucie JM; Hemophilia Inhibitor Research Study Investigators.

Am J Hematol. 2015 Oct;90(10):871-6. doi: 10.1002/ajh.24104. Epub 2015 Sep 10.


High factor VIII, von Willebrand factor, and fibrinogen levels and risk of venous thromboembolism in blacks and whites.

Payne AB, Miller CH, Hooper WC, Lally C, Austin HD.

Ethn Dis. 2014 Spring;24(2):169-74.


The CDC Hemophilia B mutation project mutation list: a new online resource.

Li T, Miller CH, Payne AB, Craig Hooper W.

Mol Genet Genomic Med. 2013 Nov;1(4):238-45. doi: 10.1002/mgg3.30. Epub 2013 Aug 19.


Mutation analysis of a cohort of US patients with hemophilia B.

Li T, Miller CH, Driggers J, Payne AB, Ellingsen D, Hooper WC.

Am J Hematol. 2014 Apr;89(4):375-9. doi: 10.1002/ajh.23645. Epub 2014 Mar 3.


Novel Polyfermentor intestinal model (PolyFermS) for controlled ecological studies: validation and effect of pH.

Zihler Berner A, Fuentes S, Dostal A, Payne AN, Vazquez Gutierrez P, Chassard C, Grattepanche F, de Vos WM, Lacroix C.

PLoS One. 2013 Oct 30;8(10):e77772. doi: 10.1371/journal.pone.0077772. eCollection 2013.


Seroepidemiologic survey of epidemic cholera in Haiti to assess spectrum of illness and risk factors for severe disease.

Jackson BR, Talkington DF, Pruckler JM, Fouché MDB, Lafosse E, Nygren B, Gómez GA, Dahourou GA, Archer WR, Payne AB, Hooper WC, Tappero JW, Derado G, Magloire R, Gerner-Smidt P, Freeman N, Boncy J, Mintz ED, The Cholera Serosurvey Working Group.

Am J Trop Med Hyg. 2013 Oct;89(4):654-664. doi: 10.4269/ajtmh.13-0208.


Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia.

Bean CJ, Boulet SL, Yang G, Payne AB, Ghaji N, Pyle ME, Hooper WC, Bhatnagar P, Keefer J, Barron-Casella EA, Casella JF, Debaun MR.

Br J Haematol. 2013 Oct;163(2):268-76. doi: 10.1111/bjh.12507. Epub 2013 Aug 16.


Fusidic acid is an effective treatment against Toxoplasma gondii and Listeria monocytogenes in vitro, but not in mice.

Payne AJ, Neal LM, Knoll LJ.

Parasitol Res. 2013 Nov;112(11):3859-63. doi: 10.1007/s00436-013-3574-1. Epub 2013 Aug 16.


Invasive pneumococcal disease among children with and without sickle cell disease in the United States, 1998 to 2009.

Payne AB, Link-Gelles R, Azonobi I, Hooper WC, Beall BW, Jorgensen JH, Juni B, Moore M; Active Bacterial Core Surveillance Team.

Pediatr Infect Dis J. 2013 Dec;32(12):1308-12. doi: 10.1097/INF.0b013e3182a11808.


Association between baseline fetal hemoglobin levels and incidence of severe vaso-occlusive pain episodes in children with sickle cell anemia.

Bhatnagar P, Keefer JR, Casella JF, Barron-Casella EA, Bean CJ, Hooper CW, Payne AB, Arking DE, Debaun MR.

Pediatr Blood Cancer. 2013 Oct;60(10):E125-7. doi: 10.1002/pbc.24588. Epub 2013 May 15.


The CDC Hemophilia A Mutation Project (CHAMP) mutation list: a new online resource.

Payne AB, Miller CH, Kelly FM, Michael Soucie J, Craig Hooper W.

Hum Mutat. 2013 Feb;34(2):E2382-91. doi: 10.1002/humu.22247. Epub 2012 Dec 26.


Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease.

Bean CJ, Boulet SL, Ellingsen D, Pyle ME, Barron-Casella EA, Casella JF, Payne AB, Driggers J, Trau HA, Yang G, Jones K, Ofori-Acquah SF, Hooper WC, DeBaun MR.

Blood. 2012 Nov 1;120(18):3822-8. doi: 10.1182/blood-2011-06-361642. Epub 2012 Sep 10.


Magnetic resonance angiography-defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose-6-phosphate dehydrogenase mutation in children with sickle cell anaemia.

Thangarajh M, Yang G, Fuchs D, Ponisio MR, McKinstry RC, Jaju A, Noetzel MJ, Casella JF, Barron-Casella E, Hooper WC, Boulet SL, Bean CJ, Pyle ME, Payne AB, Driggers J, Trau HA, Vendt BA, Rodeghier M, DeBaun MR.

Br J Haematol. 2012 Nov;159(3):352-9. doi: 10.1111/bjh.12034. Epub 2012 Sep 7.


The composition and metabolic activity of child gut microbiota demonstrate differential adaptation to varied nutrient loads in an in vitro model of colonic fermentation.

Payne AN, Chassard C, Banz Y, Lacroix C.

FEMS Microbiol Ecol. 2012 Jun;80(3):608-23. doi: 10.1111/j.1574-6941.2012.01330.x. Epub 2012 Mar 27.

Supplemental Content

Loading ...
Support Center