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Page 1
Mutation analysis of a cohort of US patients with hemophilia B.
Li T, Miller CH, Driggers J, Payne AB, Ellingsen D, Hooper WC. Li T, et al. Among authors: driggers j. Am J Hematol. 2014 Apr;89(4):375-9. doi: 10.1002/ajh.23645. Epub 2014 Mar 3. Am J Hematol. 2014. PMID: 24375831 Free PMC article.
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. Bean CJ, et al. Among authors: driggers j. Blood. 2012 Nov 1;120(18):3822-8. doi: 10.1182/blood-2011-06-361642. Epub 2012 Sep 10. Blood. 2012. PMID: 22966170 Free PMC article.
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. Thangarajh M, et al. Among authors: driggers j. Br J Haematol. 2012 Nov;159(3):352-9. doi: 10.1111/bjh.12034. Epub 2012 Sep 7. Br J Haematol. 2012. PMID: 22958163 Free PMC article. Clinical Trial.
64 results