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Use of capillary blood to diagnose hereditary spherocytosis.
Crisp RL, Solari L, Gammella D, Schvartzman GA, Rapetti MC, Donato H. Crisp RL, et al. Among authors: gammella d. Pediatr Blood Cancer. 2012 Dec 15;59(7):1299-301. doi: 10.1002/pbc.24157. Epub 2012 Apr 5. Pediatr Blood Cancer. 2012. PMID: 22488885
A prospective study to assess the predictive value for hereditary spherocytosis using five laboratory tests (cryohemolysis test, eosin-5'-maleimide flow cytometry, osmotic fragility test, autohemolysis test, and SDS-PAGE) on 50 hereditary spherocytosis families in Argentina.
Crisp RL, Solari L, Vota D, García E, Miguez G, Chamorro ME, Schvartzman GA, Alfonso G, Gammella D, Caldarola S, Riccheri C, Vittori D, Venegas B, Nesse A, Donato H. Crisp RL, et al. Among authors: gammella d. Ann Hematol. 2011 Jun;90(6):625-34. doi: 10.1007/s00277-010-1112-0. Epub 2010 Nov 16. Ann Hematol. 2011. PMID: 21080168
Red blood cell aquaporin-1 expression is decreased in hereditary spherocytosis.
Crisp RL, Maltaneri RE, Vittori DC, Solari L, Gammella D, Schvartzman G, García E, Rapetti MC, Donato H, Nesse A. Crisp RL, et al. Among authors: gammella d. Ann Hematol. 2016 Oct;95(10):1595-601. doi: 10.1007/s00277-016-2757-0. Epub 2016 Jul 28. Ann Hematol. 2016. PMID: 27465156