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Validation of the chromogenic Bethesda assay for factor VIII inhibitors in hemophilia a patients receiving Emicizumab.
Miller CH, Boylan B, Payne AB, Driggers J, Bean CJ. Miller CH, et al. Among authors: payne ab. Int J Lab Hematol. 2020 Nov 10. doi: 10.1111/ijlh.13384. Online ahead of print. Int J Lab Hematol. 2020. PMID: 33174329 No abstract available.
Trends in Sickle Cell Disease-Related Mortality in the United States, 1979 to 2017.
Payne AB, Mehal JM, Chapman C, Haberling DL, Richardson LC, Bean CJ, Hooper WC. Payne AB, et al. Ann Emerg Med. 2020 Sep;76(3S):S28-S36. doi: 10.1016/j.annemergmed.2020.08.009. Ann Emerg Med. 2020. PMID: 32928459 Free PMC article.
Coronavirus Disease among Persons with Sickle Cell Disease, United States, March 20-May 21, 2020.
Panepinto JA, Brandow A, Mucalo L, Yusuf F, Singh A, Taylor B, Woods K, Payne AB, Peacock G, Schieve LA. Panepinto JA, et al. Among authors: payne ab. Emerg Infect Dis. 2020 Oct;26(10):2473-2476. doi: 10.3201/eid2610.202792. Epub 2020 Jul 8. Emerg Infect Dis. 2020. PMID: 32639228 Free PMC article.
Evaluation of pre-analytic heat treatment protocol used in the CDC Nijmegen-Bethesda assay for heat inactivation of extended half-life haemophilia treatment products.
Payne AB, Ellingsen D, Driggers J, Bean CJ, Miller CH. Payne AB, et al. Haemophilia. 2020 Jan;26(1):e28-e30. doi: 10.1111/hae.13901. Epub 2019 Dec 6. Haemophilia. 2020. PMID: 31809555 No abstract available.
Association between clinical outcomes and metformin use in adults with sickle cell disease and diabetes mellitus.
Badawy SM, Payne AB. Badawy SM, et al. Among authors: payne ab. Blood Adv. 2019 Nov 12;3(21):3297-3306. doi: 10.1182/bloodadvances.2019000838. Blood Adv. 2019. PMID: 31698459 Free PMC article.
Reagent substitution in the chromogenic Bethesda assay for factor VIII inhibitors.
Payne AB, Miller CH, Ellingsen D, Driggers J, Boylan B, Bean CJ. Payne AB, et al. Haemophilia. 2019 Sep;25(5):e342-e344. doi: 10.1111/hae.13827. Epub 2019 Jul 29. Haemophilia. 2019. PMID: 31359589 Free PMC article. 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. Kempton CL, et al. Among authors: payne ab. Blood Adv. 2018 Jul 24;2(14):1750-1755. doi: 10.1182/bloodadvances.2018019323. Blood Adv. 2018. PMID: 30037801 Free PMC article.
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. Badawy SM, et al. Among authors: payne ab. Eur J Haematol. 2018 Oct;101(4):532-541. doi: 10.1111/ejh.13140. Epub 2018 Aug 31. Eur J Haematol. 2018. PMID: 29999202 Free PMC article.
Reagent substitutions in the Centers for Disease Control and Prevention Nijmegen-Bethesda assay for factor VIII inhibitors.
Miller CH, Payne AB, Driggers J, Ellingsen D, Boylan B, Bean CJ. Miller CH, et al. Among authors: payne ab. Haemophilia. 2018 May;24(3):e116-e119. doi: 10.1111/hae.13434. Epub 2018 Mar 24. Haemophilia. 2018. PMID: 29573516 Free PMC article. No abstract available.
Low level of the plasma sphingolipid, glucosylceramide, is associated with thrombotic diseases.
Deguchi H, Navarro S, Payne AB, Elias DJ, Dowling NF, Austin HD, EspaƱa F, Medina P, Hooper WC, Griffin JH. Deguchi H, et al. Among authors: payne ab. Res Pract Thromb Haemost. 2017 Jul;1(1):33-40. doi: 10.1002/rth2.12018. Epub 2017 Jun 23. Res Pract Thromb Haemost. 2017. PMID: 29202121 Free PMC article.
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