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Molecular immunohaematology round table discussions at the AABB Annual Meeting, Boston 2012.
Flegel WA, Johnson ST, Keller MA, Klapper EB, Khuu HM, Moulds JM, Seltsam AW, Stack G, St-Louis M, Tormey CA, Wagner FF, Weinstock C, Yazer MH, Denomme GA. Flegel WA, et al. Among authors: johnson st, st louis m. Blood Transfus. 2014 Apr;12(2):280-6. doi: 10.2450/2013.0022-13. Epub 2013 Oct 18. Blood Transfus. 2014. PMID: 24333058 Free PMC article. No abstract available.
Mass-scale red cell genotyping of blood donors.
Denomme GA, Johnson ST, Pietz BC. Denomme GA, et al. Among authors: johnson st. Transfus Apher Sci. 2011 Feb;44(1):93-9. doi: 10.1016/j.transci.2010.12.012. Epub 2011 Feb 2. Transfus Apher Sci. 2011. PMID: 21292556 Review.
It's time to phase in RHD genotyping for patients with a serologic weak D phenotype. College of American Pathologists Transfusion Medicine Resource Committee Work Group.
Sandler SG, Flegel WA, Westhoff CM, Denomme GA, Delaney M, Keller MA, Johnson ST, Katz L, Queenan JT, Vassallo RR, Simon CD; College of American Pathologists Transfusion Medicine Resource Committee Work Group. Sandler SG, et al. Among authors: johnson st. Transfusion. 2015 Mar;55(3):680-9. doi: 10.1111/trf.12941. Epub 2014 Dec 1. Transfusion. 2015. PMID: 25438646 Free PMC article. No abstract available.
Detecting fetomaternal hemorrhage: a comparison of five methods.
Bayliss KM, Kueck BD, Johnson ST, Fueger JT, McFadden PW, Mikulski D, Gottschall JL. Bayliss KM, et al. Among authors: johnson st. Transfusion. 1991 May;31(4):303-7. doi: 10.1046/j.1537-2995.1991.31491213292.x. Transfusion. 1991. PMID: 1850569
Erythroid urea transporter deficiency due to novel JKnull alleles.
Wester ES, Johnson ST, Copeland T, Malde R, Lee E, Storry JR, Olsson ML. Wester ES, et al. Among authors: johnson st. Transfusion. 2008 Feb;48(2):365-72. doi: 10.1111/j.1537-2995.2007.01532.x. Epub 2007 Nov 19. Transfusion. 2008. PMID: 18028269
214 results