1,721,012 research outputs found
Prevalence of anti-FVIII antibodies in severe haemophilia A patients with inversion of intron 22
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Homozygous patients with APC resistance may remain paucisymptomatic or asymptomatic during oral contraception.
No full textMARKED BUT TRANSITORY ELEVATION OF HEPATIC TRANSAMINASES AFTER SUBCUTANEOUS CALCIUM HEPARIN ADMINISTRATION
No full textMYELODYSPLASTIC SYNDROME AND THROMBOCYTOSIS - A RANDOM ASSOCIATION
No full textWe describe a case characterized by the onset of bone marrow hypoplasia. After treatment with steroid and anabolic compounds, it evolved into a myelodysplastic syndrome (MDS) as demonstrated by morphological and karyotypic analysis. Despite the dysplastic nature of the disorder, a unique feature was its association with a high platelet count. The pathogenesis of the thrombocytosis could not be clearly identified. In fact, the course of the disease was complicated by severe infections that, together with therapy, could have played some role in stimulating thrombopoiesis. However, since MDS can precede or follow a chronic myeloproliferative disease, it is also possible that the platelet elevation in our patient could have been sustained by a primitive thrombocyte disorder
Unexpected low prevalence of FVIII gene inversion in severe hemophilia A patients from north-eastern Italy
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"Pseudo homozygous" activated protein C resistance due to double heterozygous factor V defects (factor V Leiden mutation and type I quantitative factor V defect) associated with thrombosis: report of two cases belonging to two unrelated kindreds.
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HIGH-INCIDENCE OF NONINHIBITORY ANTI-FACTOR-VIII (FVII) ANTIBODIES IN HEMOPHILIA-A PATIENTS - RELEVANCE ON FVIII HALF-LIFE
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