Sfoglia per Autore
Single nucleotide variant rs2232710 in the protein Z-dependent protease inhibitor (ZPI, SERPINA10) gene is not associated with deep vein thrombosis
2016 M.M. Gorski, L.A. Lotta, E. Pappalardo, H.G. de Haan, S.M. Passamonti, A. van Hylckama Vlieg, I. Martinelli, F. Peyvandi
Immunochip analysis identifies novel susceptibility loci in the human leukocyte antigen region for acquired thrombotic thrombocytopenic purpura
2016 I. Mancini, I. Ricano-Ponce, E. Pappalardo, A. Cairo, M.M. Gorski, G. Casoli, B. Ferrari, M. Alberti, D. Mikovic, M. Noris, C. Wijmenga, F. Peyvandi, E. Rinaldi, A. Melpignano, S. Campus, R.A. Podda, C. Caria, A. Caddori, E. Di Francesco, G. Giuffrida, V. Agostini, U. Roncarati, C. Mannarella, A. Fragasso, G.M. Podda, E. Bertinato, A.M. Cerbone, A. Tufano, G. Loffredo, V. Poggi, M. Pizzuti, G. Re, M. Ronchi, K. Codeluppi, L. Facchini, A. De Fanti, S. Amarri, S.M. Trisolini, S. Capria, L. Aprile, M. Defina, S. Ceru
Degradation dynamics of micrornas revealed by a novel pulse-chase approach
2016 M.J. Marzi, F. Ghini, B. Cerruti, S. De Pretis, P. Bonetti, C. Giacomelli, M.M. Gorski, T. Kress, M. Pelizzola, H. Muller, B. Amati, F. Nicassio
Whole-exome sequencing to identify genetic risk variants underlying inhibitor development in severe hemophilia A patients
2016 M.M. Gorski, K. Blighe, L.A. Lotta, E. Pappalardo, I. Garagiola, I. Mancini, M.E. Mancuso, M.R. Fasulo, E. Santagostino, F. Peyvandi
The ISTH Bleeding Assessment Tool and the risk of future bleeding
2018 M.R. Fasulo, E. Biguzzi, M. Abbattista, F. Stufano, M.T. Pagliari, I. Mancini, M.M. Gorski, A. Cannavò, M. Corgiolu, F. Peyvandi, F.R. Rosendaal
Next-generation DNA sequencing to identify novel genetic risk factors for cerebral vein thrombosis
2018 M.M. Gorski, H.G. de Haan, I. Mancini, L.A. Lotta, P. Bucciarelli, S.M. Passamonti, A. Cairo, E. Pappalardo, A. van Hylckama Vlieg, I. Martinelli, F.R. Rosendaal, F. Peyvandi
Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes
2018 H.G. de Haan, A. van Hylckama Vlieg, L.A. Lotta, M.M. Gorski, P. Bucciarelli, I. Martinelli, T.P. Baglin, F. Payvandi, F.R. Rosendaal, P. Amouyel, M. de Andrade, S. Basu, C. Berr, J.A. Brody, D.I. Chasman, J.-. Dartigues, A.R. Folsom, M. Germain, J. Heit, J. Houwing-Duitermaat, C. Kabrhel, P. Kraft, G. Le Gal, S. Lindström, R. Monajemi, P.-. Morange, B.M. Psaty, P.H. Reitsma, P.M. Ridker, L.M. Rose, N. Saut, E. Slagboom, D. Smadja, N.L. Smith, P. Suchon, W. Tang, K.D. Taylor, D.-. Trégouët, C. Tzourio, M.C.H. de Visser, L.-. Weng, K.L. Wiggins
Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects
2019 M.M. Gorski, A. Lecchi, E.A. Femia, S. La Marca, A. Cairo, E. Pappalardo, L.A. Lotta, A. Artoni, F. Peyvandi
Genetic variants at the chromosomal region 2q21.3 underlying inhibitor development in patients with severe haemophilia A
2022 S. Spena, A. Cairo, E. Pappalardo, M.M. Gorski, I. Garagiola, S. Hassan, R. Gualtierotti, F. Peyvandi
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