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PUBMED FOR HANDHELDS

Journal Abstract Search


262 related items for PubMed ID: 3389894

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  • 2. The genetics and pathogenesis of haemolytic uraemic syndrome and thrombotic thrombocytopenic purpura.
    Richards A, Goodship JA, Goodship TH.
    Curr Opin Nephrol Hypertens; 2002 Jul; 11(4):431-5. PubMed ID: 12105394
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  • 5. Aetiology and pathogenesis of thrombotic thrombocytopenic purpura and haemolytic uraemic syndrome: the role of von Willebrand factor-cleaving protease.
    Furlan M, Lämmle B.
    Best Pract Res Clin Haematol; 2001 Jun; 14(2):437-54. PubMed ID: 11686108
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  • 6. [Familial, recurring plasma infusion dependent thrombotic thrombocytopenic purpura/hemolytic uremic syndrome].
    Litwin M, Smirska E.
    Pol Merkur Lekarski; 2000 Apr; 8(46):289-90. PubMed ID: 10897656
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  • 7. How I treat thrombotic thrombocytopenic purpura and atypical haemolytic uraemic syndrome.
    Scully M, Goodship T.
    Br J Haematol; 2014 Mar; 164(6):759-66. PubMed ID: 24387053
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  • 8. Clinical and laboratory patterns of the haemolytic uraemic syndrome and thrombotic thrombocytopenic purpura in southern Iran.
    Karimi M, Sabzi A, Peyvandi F, Mannucci PM.
    Intern Emerg Med; 2006 Mar; 1(1):35-9. PubMed ID: 16941811
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  • 9. von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome.
    Furlan M, Robles R, Galbusera M, Remuzzi G, Kyrle PA, Brenner B, Krause M, Scharrer I, Aumann V, Mittler U, Solenthaler M, Lämmle B.
    N Engl J Med; 1998 Nov 26; 339(22):1578-84. PubMed ID: 9828245
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  • 10. Hypocomplementemia discloses genetic predisposition to hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: role of factor H abnormalities. Italian Registry of Familial and Recurrent Hemolytic Uremic Syndrome/Thrombotic Thrombocytopenic Purpura.
    Noris M, Ruggenenti P, Perna A, Orisio S, Caprioli J, Skerka C, Vasile B, Zipfel PF, Remuzzi G.
    J Am Soc Nephrol; 1999 Feb 26; 10(2):281-93. PubMed ID: 10215327
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  • 14. Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease.
    Caprioli J, Castelletti F, Bucchioni S, Bettinaglio P, Bresin E, Pianetti G, Gamba S, Brioschi S, Daina E, Remuzzi G, Noris M, International Registry of Recurrent and Familial HUS/TTP.
    Hum Mol Genet; 2003 Dec 15; 12(24):3385-95. PubMed ID: 14583443
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  • 15. Renal transplantation in adults with thrombotic thrombocytopenic purpura/haemolytic-uraemic syndrome.
    Conlon PJ, Brennan DC, Pfaf WW, Finn WF, Gehr T, Bollinger RR, Smith SR.
    Nephrol Dial Transplant; 1996 Sep 15; 11(9):1810-4. PubMed ID: 8918627
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  • 16. Letter: Plasma-C3 in haemolytic-uraemic syndrome and thrombotic thrombocytopenic purpura.
    Cameron JS, Vick R.
    Lancet; 1973 Oct 27; 2(7835):975. PubMed ID: 4795545
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  • 18. Outcome of thrombotic thrombocytopenic purpura and hemolytic uremic syndrome in Japan.
    Mori Y, Wada H, Tamaki S, Minami N, Shiku H, Ihara T, Omine M, Kakisita E.
    Clin Appl Thromb Hemost; 1999 Apr 27; 5(2):110-2. PubMed ID: 10725990
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