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Page 1
Red blood cell membrane defects.
Iolascon A, Perrotta S, Stewart GW. Iolascon A, et al. Among authors: stewart gw. Rev Clin Exp Hematol. 2003 Mar;7(1):22-56. Rev Clin Exp Hematol. 2003. PMID: 14692233 Review.
The "stomatin" gene and protein in overhydrated hereditary stomatocytosis.
Fricke B, Argent AC, Chetty MC, Pizzey AR, Turner EJ, Ho MM, Iolascon A, von Düring M, Stewart GW. Fricke B, et al. Among authors: stewart gw. Blood. 2003 Sep 15;102(6):2268-77. doi: 10.1182/blood-2002-06-1705. Epub 2003 May 15. Blood. 2003. PMID: 12750157 Free article.
Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1.
Bruce LJ, Robinson HC, Guizouarn H, Borgese F, Harrison P, King MJ, Goede JS, Coles SE, Gore DM, Lutz HU, Ficarella R, Layton DM, Iolascon A, Ellory JC, Stewart GW. Bruce LJ, et al. Among authors: stewart gw. Nat Genet. 2005 Nov;37(11):1258-63. doi: 10.1038/ng1656. Epub 2005 Oct 9. Nat Genet. 2005. PMID: 16227998
Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1.
Andolfo I, Alper SL, De Franceschi L, Auriemma C, Russo R, De Falco L, Vallefuoco F, Esposito MR, Vandorpe DH, Shmukler BE, Narayan R, Montanaro D, D'Armiento M, Vetro A, Limongelli I, Zuffardi O, Glader BE, Schrier SL, Brugnara C, Stewart GW, Delaunay J, Iolascon A. Andolfo I, et al. Among authors: stewart gw. Blood. 2013 May 9;121(19):3925-35, S1-12. doi: 10.1182/blood-2013-02-482489. Epub 2013 Mar 11. Blood. 2013. PMID: 23479567 Free article.
A second locus mapping to 2q35-36 for familial pseudohyperkalaemia.
Carella M, d'Adamo AP, Grootenboer-Mignot S, Vantyghem MC, Esposito L, D'Eustacchio A, Ficarella R, Stewart GW, Gasparini P, Delaunay J, Iolascon A. Carella M, et al. Among authors: stewart gw. Eur J Hum Genet. 2004 Dec;12(12):1073-6. doi: 10.1038/sj.ejhg.5201280. Eur J Hum Genet. 2004. PMID: 15470366
142 results