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Hereditary dehydrated and overhydrated stomatocytosis: recent advances.
Delaunay J, Stewart G, Iolascon A. Delaunay J, et al. Among authors: stewart g. Curr Opin Hematol. 1999 Mar;6(2):110-4. doi: 10.1097/00062752-199903000-00009. Curr Opin Hematol. 1999. PMID: 10088641 Review.
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
Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus to chromosome 16 (16q23-qter).
Carella M, Stewart G, Ajetunmobi JF, Perrotta S, Grootenboer S, Tchernia G, Delaunay J, Totaro A, Zelante L, Gasparini P, Iolascon A. Carella M, et al. Among authors: stewart g. Am J Hum Genet. 1998 Sep;63(3):810-6. doi: 10.1086/302024. Am J Hum Genet. 1998. PMID: 9718354 Free PMC article.
ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders.
King MJ, Garçon L, Hoyer JD, Iolascon A, Picard V, Stewart G, Bianchi P, Lee SH, Zanella A; International Council for Standardization in Haematology. King MJ, et al. Among authors: stewart g. Int J Lab Hematol. 2015 Jun;37(3):304-25. doi: 10.1111/ijlh.12335. Epub 2015 Mar 18. Int J Lab Hematol. 2015. PMID: 25790109
South-east Asian ovalocytosis and the cryohydrocytosis form of hereditary stomatocytosis show virtually indistinguishable cation permeability defects.
Guizouarn H, Borgese F, Gabillat N, Harrison P, Goede JS, McMahon C, Stewart GW, Bruce LJ. Guizouarn H, et al. Among authors: stewart gw. Br J Haematol. 2011 Mar;152(5):655-64. doi: 10.1111/j.1365-2141.2010.08454.x. Epub 2011 Jan 23. Br J Haematol. 2011. PMID: 21255002
Stomatin is mis-trafficked in the erythrocytes of overhydrated hereditary stomatocytosis, and is absent from normal primitive yolk sac-derived erythrocytes.
Fricke B, Parsons SF, Knöpfle G, von Düring M, Stewart GW. Fricke B, et al. Among authors: stewart gw. Br J Haematol. 2005 Oct;131(2):265-77. doi: 10.1111/j.1365-2141.2005.05742.x. Br J Haematol. 2005. PMID: 16197460
Membrane raft actin deficiency and altered Ca2+-induced vesiculation in stomatin-deficient overhydrated hereditary stomatocytosis.
Wilkinson DK, Turner EJ, Parkin ET, Garner AE, Harrison PJ, Crawford M, Stewart GW, Hooper NM. Wilkinson DK, et al. Among authors: stewart gw. Biochim Biophys Acta. 2008 Jan;1778(1):125-32. doi: 10.1016/j.bbamem.2007.09.016. Epub 2007 Sep 29. Biochim Biophys Acta. 2008. PMID: 17961506
Four new cases of stomatin-deficient hereditary stomatocytosis syndrome: association of the stomatin-deficient cryohydrocytosis variant with neurological dysfunction.
Fricke B, Jarvis HG, Reid CD, Aguilar-Martinez P, Robert A, Quittet P, Chetty M, Pizzey A, Cynober T, Lande WF, Mentzer WC, Düring M, Winter S, Delaunay J, Stewart GW. Fricke B, et al. Among authors: stewart gw. Br J Haematol. 2004 Jun;125(6):796-803. doi: 10.1111/j.1365-2141.2004.04965.x. Br J Haematol. 2004. PMID: 15180870
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.
Hemolytic disease due to membrane ion channel disorders.
Stewart GW. Stewart GW. Curr Opin Hematol. 2004 Jul;11(4):244-50. doi: 10.1097/01.moh.0000132240.20671.33. Curr Opin Hematol. 2004. PMID: 15314523 Review.
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