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Rapid discrimination of the phenotypic variants of von Willebrand disease.
Roberts JC, Morateck PA, Christopherson PA, Yan K, Hoffmann RG, Gill JC, Montgomery RR; Zimmerman Program Investigators. Roberts JC, et al. Among authors: christopherson pa. Blood. 2016 May 19;127(20):2472-80. doi: 10.1182/blood-2015-11-664680. Epub 2016 Feb 25. Blood. 2016. PMID: 26917779 Free PMC article. Clinical Trial.
Common VWF exon 28 polymorphisms in African Americans affecting the VWF activity assay by ristocetin cofactor.
Flood VH, Gill JC, Morateck PA, Christopherson PA, Friedman KD, Haberichter SL, Branchford BR, Hoffmann RG, Abshire TC, Di Paola JA, Hoots WK, Leissinger C, Lusher JM, Ragni MV, Shapiro AD, Montgomery RR. Flood VH, et al. Among authors: christopherson pa. Blood. 2010 Jul 15;116(2):280-6. doi: 10.1182/blood-2009-10-249102. Epub 2010 Mar 15. Blood. 2010. PMID: 20231421 Free PMC article.
VWF mutations and new sequence variations identified in healthy controls are more frequent in the African-American population.
Bellissimo DB, Christopherson PA, Flood VH, Gill JC, Friedman KD, Haberichter SL, Shapiro AD, Abshire TC, Leissinger C, Hoots WK, Lusher JM, Ragni MV, Montgomery RR. Bellissimo DB, et al. Among authors: christopherson pa. Blood. 2012 Mar 1;119(9):2135-40. doi: 10.1182/blood-2011-10-384610. Epub 2011 Dec 23. Blood. 2012. PMID: 22197721 Free PMC article.
39 results