Search Results - "MORATELLI, S."
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1
Efficacy and safety during formulation switch of a pasteurized VWF/FVIII concentrate: results from an Italian prospective observational study in patients with von Willebrand disease
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-01-2013)“…Summary Von Willebrand disease (VWD) is an inherited bleeding disorder caused by the quantitative or qualitative deficiency of von Willebrand factor (VWF)…”
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2
A web-based registry of inherited bleeding disorders in the region of Emilia-Romagna: results at three and a half years
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-03-2008)“…A Registry of inherited bleeding disorders was set up in the Region of Emilia‐Romagna (RER) to collect information about these diseases and to improve the…”
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3
Production of full-length cDNA sequences by sequencing and analysis of expressed sequence tags from Schistosoma mansoni
Published in Memórias do Instituto Oswaldo Cruz (01-10-2006)“…The number of sequences generated by genome projects has increased exponentially, but gene characterization has not followed at the same rate. Sequencing and…”
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4
Long-lasting remission and successful treatment of acquired factor VIII inhibitors using cyclophosphamide in a patient with systemic lupus erythematosus
Published in Rheumatology (Oxford, England) (01-10-1999)“…Acquired deficiency of clotting factor VIII (FVIII) is a rare bleeding diathesis seldom encountered in systemic lupus erythematosus (SLE). Reduction of FVIII…”
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5
Demographic and clinical data in acquired hemophilia A: results from the European Acquired Haemophilia Registry (EACH2)
Published in Journal of thrombosis and haemostasis (01-04-2012)“…Background: Acquired hemophilia A (AHA) is a rare autoimmune disease caused by autoantibodies against coagulation factor VIII and characterized by spontaneous…”
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6
Management of bleeding in acquired hemophilia A: results from the European Acquired Haemophilia (EACH2) Registry
Published in Blood (05-07-2012)“…Acquired hemophilia A is a rare bleeding disorder caused by autoantibodies to coagulation FVIII. Bleeding episodes at presentation are spontaneous and severe…”
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Thrombotic risk in thalassemic patients
Published in Journal of pediatric endocrinology & metabolism : JPEM (1998)“…Hemostatic parameters of 495 beta-thalassemic patients (421 with thalassemia major and 74 with thalassemia intermedia) were analyzed, to assess their…”
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The reduced sensitivity of the ProC® Global test in protein S deficient subjects reflects a reduction in the associated thrombotic risk
Published in Blood coagulation & fibrinolysis (01-12-2001)“…To investigate simultaneously a defect affecting the protein C/protein S (PC/PS) anticoagulant pathway is possible thanks to a methodological approach (ProC…”
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Coexistence of antithrombin deficiency, factor V Leiden and hyperhomocysteinemia in a thrombotic family
Published in Blood coagulation & fibrinolysis (01-01-1998)“…We report a thrombotic family with combined type I antithrombin deficiency and factor V Leiden (factor V-R506Q) in which the proposita, affected by recurrent…”
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Resistance to activated protein C and low levels of protein S activity in nine thrombophilic families: a correct diagnosis
Published in Blood coagulation & fibrinolysis (01-03-1997)“…In order to define the thrombophilic conditions related to activated protein C resistance (APC-R) and protein S (PS) deficiency and to detect the possible…”
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A novel mutation (Leu817Pro) causing type 2A von Willebrand disease
Published in British journal of haematology (01-01-1996)“…We studied a patient affected by von Willebrand disease type 2A who experienced several mild bleeding episodes and was characterized by markedly reduced…”
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Coexistence of factor V G1691A and factor II G20210A gene mutations in a thrombotic family is associated with recurrence and early onset of venous thrombosis
Published in Haemostasis (01-03-2001)“…Two G-to-A mutations at positions 1691 of the factor V (FV) gene and 20210 of the prothrombin (FII) gene have been associated with an increased risk of venous…”
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13
Anticardiolipin antibody-related thrombocytopenia: persistent remission after splenectomy
Published in Haematologica (Roma) (01-05-1995)“…Center for the Study of Haemostasis and Thrombosis, University of Ferrara, Italy. The lupus anticoagulant (LAC) and anticardiolipin antibody (ACA) syndromes…”
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14
Pattern of iron excretion in relation to haemoglobin level and iron load in 8 haematological patients following the administration of subcutaneous deferrioxamine
Published in European journal of haematology (01-10-1994)“…Iron excretion following subcutaneous administration of deferrioxamine (DFO) was measured between two transfusions of packed red cells in 6 patients with…”
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A web-based clinical record 'xl'Emofilia®' for outpatients with haemophilia and allied disorders in the Region of Emilia-Romagna: features and pilot use
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01-01-2009)“…The treatment of haemophilia in developed countries is based on home self‐infusion of concentrates. Improving communication between haemophilia centres (HC)…”
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16
BNDb--Biomolecules Nucleus Database: an integrated proteomics and transcriptomics database
Published in Genetics and molecular research (01-01-2007)“…Proteomics correspond to the identification and quantitative analysis of proteins expressed in different conditions or life stages of a cell or organism…”
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A common mutation in the gene for coagulation factor XIII‐A (VAL34Leu): A risk factor for primary intracerebral hemorrhage is protective against atherothrombotic diseases
Published in American journal of hematology (01-07-2001)“…The role of a common polymorphism in the factor XIII A‐subunit gene (FXIII Val34Leu) has been recently investigated as a protective genetic factor against…”
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18
Low Folate Levels and Thermolabile Methylenetetrahydrofolate Reductase as Primary Determinant of Mild Hyperhomocystinemia in Normal and Thromboembolic Subjects
Published in Arteriosclerosis, thrombosis, and vascular biology (01-07-1999)“…Several studies have indicated that mild to moderate hyperhomocystinemia is a common cause of arterial occlusive disease. Whether hyperhomocystinemia per se is…”
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19
Production of full-length cDNA sequences by sequencing and analysis of expressed sequence tags from Schistosoma mansoni
Published in Memórias do Instituto Oswaldo Cruz (11-01-2007)“…The number of sequences generated by genome projects has increased exponentially, but gene characterization has not followed at the same rate. Sequencing and…”
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20
The G to T point mutation (Val34Leu) in the Factor XIII-A subunit gene in venous leg ulcers
Published in Journal of thrombosis and haemostasis (01-07-2003)Get full text
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