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Thrombofilic genotypes in subjects with idiopathic antiphospholipid antibodies-prevalence and significance 1-gen-1998 Ames, Pr; Tommasino, C; D'Andrea, Giovanna; Iannaccone, L; Brancaccio, V; Margaglione, Maurizio
Plasminogen activator inhibitor-1 (PAI-1) plasma levels in a general population without clinical evidence of atherosclerosis. Relation to environmental and genetic determinants. 1-gen-1998 Margaglione, Maurizio; Cappucci, G; D’Addedda, M; Colaizzo, D; Giuliani, N; Vecchione, G; Mascolo, G; Grandone, E; Di Minno, G.
Methylenetetrahydrofolate reductase (MTHFR) 677T-> C mutation and unexplained early pregnancy loss 1-gen-1998 Grandone, E; Margaglione, Maurizio; Colaizzo, D; D'Addedda, M; D'Andrea, Giovanna; Pavone, G; THROMB HAEMOST, DI MINNO G. METHYLENETETRAHYDROFOLATE REDUCTASE MTHFR T. C. MUTATION AND UNEXPLAINED EARLY PREGNANCY L. O. S. S.; .,
Identifying human platelet glycoproteins IIb and IIIa by capillary electhrophoresis. 1-gen-1998 Vecchione, G; Margaglione, Maurizio; Grandone, E; Colaizzo, D; Cappucci, G; Giuliani, N; D’Addedda, M; D’Andrea, G; Nobile, M; Amoriello, A; Di Minno, G.
Identifying human platelet glycoproteins IIb and IIla by capillary electrophoresis 1-gen-1998 Vecchione, G; Margaglione, Maurizio; Grandone, E.; Colaizzo, D.; Cappucci, G.; Giuliani, N.; D'Addedda, M.; D'Andrea, Giovanna; Nobile, M.; Amoriello, A.; Di Minno, G.
Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (factor V Leiden). 1-gen-1999 Faioni, Em; Franchi, F; Bucciarelli, P; Margaglione, Maurizio; DE STEFANO, V; Castaman, G; Finazzi, G; Mannucci, P. M.
Prothrombotic genetic risk factors in young survivors of myocardial infarction. 1-gen-1999 Ardissino, D; Mannucci, Pm; Merlini, Pa; Duca, F; Fetiveau, R; Tagliabue, L; Tubaro, M; Galvani, M; Ottani, F; Ferrario, M; Corral, J; Margaglione, Maurizio
The use of frozen-thawed platelet-derived phospholipids as a confirmatory test for the diagnosis of Lupus Anticoagulants. Comparison with two commercial confirmatory system tests. 1-gen-1999 Cappucci, G; Grandone, E; Giuliani, N; Margaglione, Maurizio; Di Minno, G.
Prothrombotic genetic risk factors and the occurrence of gestational hypertension with or without proteinuria. 1-gen-1999 Grandone, E; Margaglione, Maurizio; Colaizzo, D; Cappucci, G; Sciannamé, N; Montanaro, S; Paladini, D; Martinelli, P; Di Minno, G.
Anticardiolipin antibodies in patients with liver disease. 1-gen-1999 Mangia, A; Margaglione, Maurizio; Cascavilla, I; Cappucci, G; Facciorusso, D; Grandone, E; Di Minno, G; Rizzetto, M; Andriulli, A.
Absence of apolipoprotein B3500 mutation in type 2a hyperlipoproteinemia patients and in the general population from southern Italy. 1-gen-1999 Seripa, D; Gravina, C; Volpe, R; Margaglione, Maurizio; Papa, S; Merla, G; Parrella, P; Di Minno, G; Ricci, G; Testa, M; Fazio, V. M.
HLA class II favors clearance of HCV infection and progression of the chronic liver damage. 1-gen-1999 Mangia, A; Gentile, R; Cascavilla, I; Margaglione, Maurizio; Villani, Mr; Stella, F; Modola, G; Agostiano, V; Gaudiano, C; Andriulli, A.
Inherited prothrombotic conditions and premature ischemic stroke. Sex difference in the association with Factor V leiden 1-gen-1999 Margaglione, Maurizio; D'Andrea, Giovanna; Giuliani, N.; Brancaccio, V.; DE LUCIA, D.; Grandone, E.; DE STEFANO, V.; Tonali, P. A.; DI MINNO, G.
Coexistence of factor V Leiden and Factor II A20210 mutations and recurrent venous thromboembolism 1-gen-1999 Margaglione, Maurizio; D'Andrea, Giovanna; Colaizzo, D. CAPPUCCI G.; DEL POPOLO, A.; Brancaccio, V.; Ciampa, A.; Grandone, V.; Diminno, G.
Compound heterozygosity (554-589 del, C-T transition) in the platelet glycoprotein iba gene in a patient with a severe bleeding tendency. 1-gen-1999 Margaglione, Maurizio; D'Andrea, Giovanna; Grandone, E; Brancaccio, V; Amoriello, A; DI MINNO, G.
ACE, PAI-1, Decorin and Werner helicase genes are not associated with the development of renal disease in European patients with type 1 diabetes. 1-gen-1999 De Cosmo, S; Margaglione, Maurizio; Tassi, V; Garrubba, M; Thomas, S; Olivetti, C; Piras, Gp; Trevisan, R; Vedovato, M; Cavallo Perin, P; Bacci, S; Colaizzo, D; Cisternino, C; Zucaro, L; Di Minno, G; Trischitta, V; Viberti, G. C.
Determining sulphur-containing aminoacids by capillary electrophoresis. A fast novel method for total homocyst(e)ine in human plasma. 1-gen-1999 Vecchione, G; Margaglione, Maurizio; Grandone, E; Colaizzo, D; Cappucci G. Fermo I., D’Angelo A; Di Minno, G.
Homocysteine, plasma function and thrombosis. 1-gen-1999 Di Minno, G; Coppola, A; Mancini, Fp; Margaglione, Maurizio
Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (mthfr) gene in offspring of patients with myocardial infarction. 1-gen-1999 Margaglione, Maurizio; Colaizzo, D; Cappucci, G; del Popolo, A; Vecchione, G; Grandone, E; Di Minno, G.
Inherited thrombophilic risk factors and venous thromboembolism: distinct role in peripheral deep venous thrombosis and pulmonary embolism. 1-gen-2000 Margaglione, Maurizio; Brancaccio, V; DE LUCIA, D; Martinelli, I; Ciampa, A; Grandone, E; DI MINNO, G.
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