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Journal Abstract Search

155 related items for PubMed ID: 22322135

  • 1.
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  • 2. Central nervous system abnormalities in asymptomatic young patients with Sbeta-thalassemia.
    Zafeiriou DI, Prengler M, Gombakis N, Kouskouras K, Economou M, Kardoulas A, Tsantali C, Dimitriadis A, Athanasiou M, Kirkham FJ.
    Ann Neurol; 2004 Jun; 55(6):835-9. PubMed ID: 15174017
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  • 4. Hypercoagulable state in five thalassemia intermedia patients.
    Bhattacharyya M, Kannan M, Chaudhry VP, Mahapatra M, Pati H, Saxena R.
    Clin Appl Thromb Hemost; 2007 Oct; 13(4):422-7. PubMed ID: 17911195
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  • 5. Plasma protein Z and protein C inhibitors and their role in hypercoagulability of thalassemia.
    Del Vecchio GC, Nigro A, Giordano P, Schettini F, Altomare M, Pietrapertosa A, De Mattia D.
    Acta Haematol; 2007 Oct; 118(3):136-40. PubMed ID: 17804900
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  • 6. Congenital thrombotic risk factors in beta-thalassemia.
    Sipahi T, Kara A, Kuybulu A, Egin Y, Akar N.
    Clin Appl Thromb Hemost; 2009 Oct; 15(5):581-4. PubMed ID: 18480081
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  • 9. Protein C and D-dimer are related to portal vein thrombosis in patients with liver cirrhosis.
    Zhang D, Hao J, Yang N.
    J Gastroenterol Hepatol; 2010 Jan; 25(1):116-21. PubMed ID: 19686413
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  • 10. Neurophysiologic and intellectual evaluation of beta-thalassemia patients.
    Economou M, Zafeiriou DI, Kontopoulos E, Gompakis N, Koussi A, Perifanis V, Athanassiou-Metaxa M.
    Brain Dev; 2006 Jan; 28(1):14-8. PubMed ID: 15925466
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  • 11. Early markers of blood coagulation and fibrinolysis activation in Argentine hemorrhagic fever.
    Heller MV, Marta RF, Sturk A, Maiztegui JI, Hack CE, Cate JW, Molinas FC.
    Thromb Haemost; 1995 Mar; 73(3):368-73. PubMed ID: 7667817
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  • 14. Alterations of anticoagulant proteins and soluble endothelial protein C receptor in thalassemia patients of Chinese origin.
    Huang Y, Long Y, Deng D, Liu Z, Liang H, Sun N, Xu Y, Lai Y, Cheng P.
    Thromb Res; 2018 Dec; 172():61-66. PubMed ID: 30384036
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  • 16. Resistance to activated protein C and low levels of free protein S in Greek patients with inflammatory bowel disease.
    Koutroubakis IE, Sfiridaki A, Mouzas IA, Maladaki A, Kapsoritakis A, Roussomoustakaki M, Kouroumalis EA, Manousos ON.
    Am J Gastroenterol; 2000 Jan; 95(1):190-4. PubMed ID: 10638581
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  • 17. The prevalence of factor V Leiden (G1691A), prothrombin G20210A and methylenetetrahydrofolate reductase C677T mutations in Jordanian patients with beta-thalassemia major.
    Al-Sweedan SA, Jaradat S, Iraqi M, Beshtawi M.
    Blood Coagul Fibrinolysis; 2009 Dec; 20(8):675-8. PubMed ID: 19710606
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  • 18. [Intracranial hemorrhage and hemostasis. Monitoring patients after intracranial hemorrhage by determination and follow-up of activation products of blood coagulation].
    Menges T, von Lessen A, Welters I, Wagner RM, Ruwoldt R, Boldt J, Hempelmann G.
    Infusionsther Transfusionsmed; 1994 Aug; 21(4):244-50. PubMed ID: 7950289
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  • 19. Hypercoagulable state as demonstrated by thromboelastometry in hemoglobin E/beta-thalassemia patients: Association with clinical severity and splenectomy status.
    Natesirinilkul R, Charoenkwan P, Nawarawong W, Boonsri S, Tantivate P, Wongjaikum S, Manowong S, Sanguansermsri T.
    Thromb Res; 2016 Apr; 140():125-131. PubMed ID: 26971311
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  • 20. Blood coagulation, fibrinolytic activity and lipid profile in subclinical thyroid disease: subclinical hyperthyroidism increases plasma factor X activity.
    Erem C.
    Clin Endocrinol (Oxf); 2006 Mar; 64(3):323-9. PubMed ID: 16487444
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