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Rhnull syndrome: identification of a novel mutation in RHce.
Rosa KA, Reid ME, Lomas-Francis C, Powell VI, Costa FF, Stinghen ST, Watanabe AM, Carboni EK, Baldon JP, Jucksch MM, Castilho L. Rosa KA, et al. Among authors: castilho l. Transfusion. 2005 Nov;45(11):1796-8. doi: 10.1111/j.1537-2995.2005.00605.x. Transfusion. 2005. PMID: 16271106
Molecular HPA genotyping by microarray in Brazilian blood donors.
Conti F, Bertrand G, Dezan M, Costa T, Aravechia M, Mota M, Castilho L, Kaplan C, Kutner J. Conti F, et al. Among authors: castilho l. Transfusion. 2014 Feb;54(2):405-11. doi: 10.1111/trf.12272. Epub 2013 Jun 13. Transfusion. 2014. PMID: 23763477
How do we identify RHD variants using a practical molecular approach?
Arnoni CP, Latini FR, Muniz JG, Gazito D, Person Rde M, de Paula Vendrame TA, Barreto JA, Castilho L. Arnoni CP, et al. Among authors: castilho l. Transfusion. 2014 Apr;54(4):962-9. doi: 10.1111/trf.12557. Epub 2014 Feb 28. Transfusion. 2014. PMID: 24579654
Variant RH alleles and Rh immunisation in patients with sickle cell disease.
Sippert E, Fujita CR, Machado D, Guelsin G, Gaspardi AC, Pellegrino J Jr, Gilli S, Saad SS, Castilho L. Sippert E, et al. Among authors: castilho l. Blood Transfus. 2015 Jan;13(1):72-7. doi: 10.2450/2014.0324-13. Epub 2014 Jun 19. Blood Transfus. 2015. PMID: 24960646 Free PMC article. Clinical Trial.
298 results