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Results: 1-16 |
Results: 16
Extensive life-threatening thrombosis in a patient with heparin-induced thrombocytopenia and factor V Leiden mutation
Authors: Pizzolo, F Girelli, D Olivieri, O
Citation: F. Pizzolo et al., Extensive life-threatening thrombosis in a patient with heparin-induced thrombocytopenia and factor V Leiden mutation, HAEMATOLOG, 86(9), 2001, pp. 1008-1008
Association of phlebotomy and subcutaneous bolus injection of deferoxaminefor the treatment of anemic patients with iron overload
Authors: Franchini, M Gandini, G Girelli, D Lippi, G de Gironcoli, M Aprili, G
Citation: M. Franchini et al., Association of phlebotomy and subcutaneous bolus injection of deferoxaminefor the treatment of anemic patients with iron overload, HAEMATOLOG, 86(8), 2001, pp. 873-874
Functional properties of factor V and factor Va encoded by the R2-gene
Authors: Hoekema, L Castoldi, E Tans, G Girelli, D Gemmati, D Bernardi, F Rosing, J
Citation: L. Hoekema et al., Functional properties of factor V and factor Va encoded by the R2-gene, THROMB HAEM, 85(1), 2001, pp. 75-81
Homozygosity for angiotensinogen 235T variant increases the risk of myocardial infarction in patients with multi-vessel coronary artery disease
Authors: Olivieri, O Stranieri, C Girelli, D Pizzolo, F Grazioli, S Russo, C Pignatti, PF Corrocher, R
Citation: O. Olivieri et al., Homozygosity for angiotensinogen 235T variant increases the risk of myocardial infarction in patients with multi-vessel coronary artery disease, J HYPERTENS, 19(5), 2001, pp. 879-884
New high performance phosphites
Authors: Costanzi, S Farris, R Girelli, D
Citation: S. Costanzi et al., New high performance phosphites, POLYM DEGR, 73(3), 2001, pp. 425-430
Polymorphisms in the factor VII gene and the risk of myocardial infarction- Reply
Authors: Girelli, D Bernardi, F Corrocher, R
Citation: D. Girelli et al., Polymorphisms in the factor VII gene and the risk of myocardial infarction- Reply, N ENG J MED, 344(6), 2001, pp. 459-459
G20210A prothrombin gene polymorphism and prothrombin activity in subjectswith or without angiographically documented coronary artery disease
Authors: Russo, C Girelli, D Olivieri, O Guarini, P Manzato, F Pizzolo, F Zaia, B Mazzucco, A Corrocher, R
Citation: C. Russo et al., G20210A prothrombin gene polymorphism and prothrombin activity in subjectswith or without angiographically documented coronary artery disease, CIRCULATION, 103(20), 2001, pp. 2436-2440
Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndrome
Authors: Girelli, D Bozzini, C Zecchina, G Tinazzi, E Bosio, S Piperno, A Ramenghi, U Peters, J Levi, S Camaschella, C Corrocher, R
Citation: D. Girelli et al., Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndrome, BR J HAEM, 115(2), 2001, pp. 334-340
Three cases of Buerger's disease associated with hyperhomocysteinemia
Authors: Caramaschi, P Biasi, D Carletto, A Friso, S Girelli, D Arcaro, G Bambara, LM
Citation: P. Caramaschi et al., Three cases of Buerger's disease associated with hyperhomocysteinemia, CLIN EXP RH, 18(2), 2000, pp. 264-265
Mutations in the R2 FV gene affect the ratio between the two FV isoforms in plasma
Authors: Castoldi, E Rosing, J Girelli, D Hoekema, L Lunghi, B Mingozzi, F Ferraresi, P Friso, S Corrocher, R Tans, G Bernardi, F
Citation: E. Castoldi et al., Mutations in the R2 FV gene affect the ratio between the two FV isoforms in plasma, THROMB HAEM, 83(3), 2000, pp. 362-365
Polymorphisms in the factor VII gene and the risk of myocardial infarctionin patients with coronary artery disease
Authors: Girelli, D Russo, C Ferraresi, P Olivieri, O Pinotti, M Friso, S Manzato, F Mazzucco, A Bernardi, F Corrocher, R
Citation: D. Girelli et al., Polymorphisms in the factor VII gene and the risk of myocardial infarctionin patients with coronary artery disease, N ENG J MED, 343(11), 2000, pp. 774-780
Haemochromatosis in patients with beta-thalassaemia trait
Authors: Piperno, A Mariani, R Arosio, C Vergani, A Bosio, S Fargion, S Sampietro, M Girelli, D Fraquelli, M Conte, D Fiorelli, G Camaschella, C
Citation: A. Piperno et al., Haemochromatosis in patients with beta-thalassaemia trait, BR J HAEM, 111(3), 2000, pp. 908-914
Combinations of 4 mutations (FV R506Q, FVH1299R, FVY1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic family
Authors: Castoldi, E Simioni, P Kalafatis, M Lunghi, B Tormene, D Girelli, D Girolami, A Bernardi, F
Citation: E. Castoldi et al., Combinations of 4 mutations (FV R506Q, FVH1299R, FVY1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic family, BLOOD, 96(4), 2000, pp. 1443-1448
Modulation of factor VII levels by intron 7 polymorphisms: population and in vitro studies
Authors: Pinotti, M Toso, R Girelli, D Bindini, D Ferraresi, P Papa, ML Corrocher, R Marchetti, G Bernardi, F
Citation: M. Pinotti et al., Modulation of factor VII levels by intron 7 polymorphisms: population and in vitro studies, BLOOD, 95(11), 2000, pp. 3423-3428
Genetic polymorphisms of the renin-angiotensin system and atheromatous renal artery stenosis
Authors: Olivieri, O Trabetti, E Grazioli, S Stranieri, C Friso, S Girelli, D Russo, C Pignatti, PF Mansueto, G Corrocher, R
Citation: O. Olivieri et al., Genetic polymorphisms of the renin-angiotensin system and atheromatous renal artery stenosis, HYPERTENSIO, 34(5), 1999, pp. 1097-1100
Is the oral methionine loading test insensitive to the remethylation pathway of homocysteine? Response
Authors: Girelli, D Olivieri, O Russo, C Corrocher, R
Citation: D. Girelli et al., Is the oral methionine loading test insensitive to the remethylation pathway of homocysteine? Response, BLOOD, 93(3), 1999, pp. 1119-1120
Risultati: 1-16 |