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Results: 1-14 |
Results: 14
The role of cysteine and homocysteine in venous and arterial thrombotic disease
Authors: Marcucci, R Brunelli, T Giusti, B Fedi, S Pepe, G Poli, D Prisco, D Abbate, R Gensini, GF
Citation: R. Marcucci et al., The role of cysteine and homocysteine in venous and arterial thrombotic disease, AM J CLIN P, 116(1), 2001, pp. 56-60
Thrombophilic risk factors in patients with central retinal vein occlusion
Authors: Marcucci, R Bertini, L Giusti, B Brunelli, T Fedi, S Cellai, AP Poli, D Pepe, G Abbate, R Prisco, D
Citation: R. Marcucci et al., Thrombophilic risk factors in patients with central retinal vein occlusion, THROMB HAEM, 86(3), 2001, pp. 772-776
The C677T methylenetetrahydrofolate reductase mutation is not associated with Alzheimer's disease
Authors: Brunelli, T Bagnoli, S Giusti, B Nacmias, B Pepe, G Sorbi, S Abbate, R
Citation: T. Brunelli et al., The C677T methylenetetrahydrofolate reductase mutation is not associated with Alzheimer's disease, NEUROSCI L, 315(1-2), 2001, pp. 103-105
Ullrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen type VI
Authors: Vanegas, OC Bertini, E Zhang, RZ Petrini, S Minosse, C Sabatelli, P Giusti, B Chu, ML Pepe, G
Citation: Oc. Vanegas et al., Ullrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen type VI, P NAS US, 98(13), 2001, pp. 7516-7521
Fibrillin-1 (FBN1) gene frameshift mutations in Marfan patients: genotype-phenotype correlation
Authors: Pepe, G Giusti, B Evangelisti, L Porciani, MC Brunelli, T Giurlani, L Attanasio, M Fattori, R Bagni, C Comeglio, P Abbate, R Gensini, GF
Citation: G. Pepe et al., Fibrillin-1 (FBN1) gene frameshift mutations in Marfan patients: genotype-phenotype correlation, CLIN GENET, 59(6), 2001, pp. 444-450
High prevalence of mild hyperhomocysteinemia in patients with abdominal aortic aneurysm
Authors: Brunelli, T Prisco, D Fedi, S Rogolino, A Farsi, A Marcucci, R Giusti, B Pratesi, C Pulli, R Gensini, GF Abbate, R Pepe, G
Citation: T. Brunelli et al., High prevalence of mild hyperhomocysteinemia in patients with abdominal aortic aneurysm, J VASC SURG, 32(3), 2000, pp. 531-536
A novel de novo mutation in the triple helix of the COL6A3 gene in a two-generation Italian family affected by Bethlem myopathy. A diagnostic approach in the mutations' screening of type VI collagen
Authors: Pepe, G Bertini, E Giusti, B Brunelli, T Comeglio, P Saitta, B Merlini, L Chu, ML Federici, G Abbate, R
Citation: G. Pepe et al., A novel de novo mutation in the triple helix of the COL6A3 gene in a two-generation Italian family affected by Bethlem myopathy. A diagnostic approach in the mutations' screening of type VI collagen, NEUROMUSC D, 9(4), 1999, pp. 264-271
High prevalence of anti-beta 2 glycoprotein I antibodies in patients with ischemic heart disease
Authors: Farsi, A Domeneghetti, MP Fedi, S Capanni, M Giusti, B Marcucci, R Giurlani, L Prisco, D Passaleva, A Gensini, GF Abbate, R
Citation: A. Farsi et al., High prevalence of anti-beta 2 glycoprotein I antibodies in patients with ischemic heart disease, AUTOIMMUN, 30(2), 1999, pp. 93-98
World distribution of the TS33C/844INS68 CBS in cis double mutation: a reliable anthropological marker
Authors: Pepe, G Vanegas, OC Rickards, O Giusti, B Comeglio, P Brunelli, T Marcucci, R Prisco, D Gensini, GF Abbate, R
Citation: G. Pepe et al., World distribution of the TS33C/844INS68 CBS in cis double mutation: a reliable anthropological marker, HUM GENET, 104(2), 1999, pp. 126-129
Percutaneous Transluminal Coronary Angioplasty procedure is associated to a decrease in Transforming Growth Factor Beta 1 levels
Authors: Falciani, M Gori, AM Giusti, B Fedi, S Capanni, M Simonetti, I Margheri, M Prisco, D Abbate, R Gensini, GF
Citation: M. Falciani et al., Percutaneous Transluminal Coronary Angioplasty procedure is associated to a decrease in Transforming Growth Factor Beta 1 levels, THROMB HAEM, 82(3), 1999, pp. 1204-1205
Tissue factor reduction and tissue factor pathway inhibitor release after heparin administration
Authors: Gori, AM Pepe, G Attanasio, M Falciani, M Abbate, R Prisco, D Fedi, S Giusti, B Brunelli, T Comeglio, P Gensini, GF Serneri, GGN
Citation: Am. Gori et al., Tissue factor reduction and tissue factor pathway inhibitor release after heparin administration, THROMB HAEM, 81(4), 1999, pp. 589-593
Microheterogeneity in the distribution of the 844ins68 in the cystathionine beta-synthase gene in Italy
Authors: Giusti, B Camacho-Vanegas, O Attanasio, M Comeglio, P Gori, AM Brunelli, T Prisco, D Gensini, GF Abbate, R Pepe, G
Citation: B. Giusti et al., Microheterogeneity in the distribution of the 844ins68 in the cystathionine beta-synthase gene in Italy, THROMB RES, 94(4), 1999, pp. 249-254
Multiple primary tumors of the upper aerodigestive tract: Is there a role for constitutional mutations in the p53 gene?
Authors: Gallo, O Sardi, I Pape, G Franchi, A Attanasio, M Giusti, B Bocciolini, C Abbate, R
Citation: O. Gallo et al., Multiple primary tumors of the upper aerodigestive tract: Is there a role for constitutional mutations in the p53 gene?, INT J CANC, 82(2), 1999, pp. 180-186
A heterozygous splice site mutation in COL6A1 leading to an in-frame deletion of the alpha 1(VI) collagen chain in an Italian family affected by Bethlem myopathy
Authors: Pepe, G Giusti, B Bertini, E Brunelli, T Saitta, B Comeglio, P Bolognese, A Merlini, L Federici, G Abbate, R Chu, ML
Citation: G. Pepe et al., A heterozygous splice site mutation in COL6A1 leading to an in-frame deletion of the alpha 1(VI) collagen chain in an Italian family affected by Bethlem myopathy, BIOC BIOP R, 258(3), 1999, pp. 802-807
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