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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

129 related items for PubMed ID: 10050708

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  • 22. Mild dehydrated hereditary stomatocytosis revealed by marked hepatosiderosis.
    Syfuss PY, Ciupea A, Brahimi S, Cynober T, Stewart GW, Grandchamp B, Beaumont C, Tchernia G, Delaunay J, Wagner JC.
    Clin Lab Haematol; 2006 Aug; 28(4):270-4. PubMed ID: 16898969
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  • 27. Dehydrated hereditary stomatocytosis mimicking familial hyperkalaemic hypertension: clinical and genetic investigation.
    Beaurain G, Mathieu F, Grootenboer S, Fiquet B, Cynober T, Tchernia G, Delaunay J, Jeunemaitre X.
    Eur J Haematol; 2007 Mar; 78(3):253-9. PubMed ID: 17253968
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  • 30. 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.
    Eur J Hum Genet; 2004 Dec; 12(12):1073-6. PubMed ID: 15470366
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  • 31. Cation-leak stomatocytosis in standard schnauzers does not cosegregate with coding mutations in the RhAG, SLC4A1, or GLUT1 genes associated with human disease.
    Shmukler BE, Rivera A, Vandorpe DH, Alves J, Bonfanti U, Paltrinieri S, Alper SL.
    Blood Cells Mol Dis; 2012 Apr 15; 48(4):219-25. PubMed ID: 22406315
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  • 32. The cation-leaky hereditary stomatocytosis syndromes: A tale of six proteins.
    Stewart GW, Gibson JS, Rees DC.
    Br J Haematol; 2023 Nov 15; 203(4):509-522. PubMed ID: 37679660
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  • 38. Hereditary xerocytosis and familial haemolysis due to mutation in the PIEZO1 gene: a simple diagnostic approach.
    Sandberg MB, Nybo M, Birgens H, Frederiksen H.
    Int J Lab Hematol; 2014 Aug 15; 36(4):e62-5. PubMed ID: 24314002
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