Search Results - "Bernardis, I." :: K.UTB vyhledávací portál

Targeted cancer exome sequencing reveals recurrent mutations in myeloproliferative neoplasms

by Tenedini, E, Bernardis, I, Artusi, V, Artuso, L, Roncaglia, E, Guglielmelli, P, Pieri, L, Bogani, C, Biamonte, F, Rotunno, G, Mannarelli, C, Bianchi, E, Pancrazzi, A, Fanelli, T, Malagoli Tagliazucchi, G, Ferrari, S, Manfredini, R, Vannucchi, A M, Tagliafico, E
Published in Leukemia (01.05.2014)

Get full text

Journal Article

Loading…

ERBB2 and PI3KCA mutations in endocrine resistant breast cancer (BC)

by Venturelli, M., Toss, A., Piacentini, F., Bernardis, I., Tenedini, E., Omarini, C., Moscetti, L., Cascinu, S., Tagliafico, E., Cortesi, L.
Published in Annals of oncology (01.09.2018)

Get full text

Journal Article

Loading…

Amplicon-based next-generation sequencing: an effective approach for the molecular diagnosis of epidermolysis bullosa

by Tenedini, E., Artuso, L., Bernardis, I., Artusi, V., Percesepe, A., De Rosa, L., Contin, R., Manfredini, R., Pellacani, G., Giannetti, A., Pagani, J., De Luca, M., Tagliafico, E.
Published in British journal of dermatology (1951) (01.09.2015)

Get full text

Journal Article

Loading…

Genetic heterogeneity of primary hpobetalipoproteinemia reveald by the next generation sequencing (NGS)

by Di Leo, E, Simone, M.L, Artuso, L, Bernardis, I, Tagliafico, E, Tarugi, P
Published in Nutrition, metabolism, and cardiovascular diseases (01.01.2017)

Get full text

Journal Article

Loading…

Molecular diagnosis of primary hypertriglyceridemias by next generation sequencing (NGS): Preliminary results and open questions

by Rabacchi, C, Tenedini, E, Bernardis, I, Simone, M.L, Tagliafico, E, Tarugi, P
Published in Nutrition, metabolism, and cardiovascular diseases (01.01.2017)

Get full text

Journal Article

Loading…

96PERBB2 and PI3KCA mutations in endocrine resistant breast cancer (BC)

by Venturelli, M, Toss, A, Piacentini, F, Bernardis, I, Tenedini, E, Omarini, C, Moscetti, L, Cascinu, S, Tagliafico, E, Cortesi, L
Published in Annals of oncology (01.09.2018)

Get full text

Journal Article

Loading…

PS-107 - Rare ceruloplasmin variants are associated with hyperferritinemia and increased hepatic iron in NAFLD patients: results from a NGS study

by Corradini, E., Bernardis, I., Dongiovanni, P., Buzzetti, E., Caleffi, A., Artuso, L., Pelusi, S., Tenedini, E., Tagliafico, E., Rametta, R., Fracanzani, A.L., Fargion, S., Pietrangelo, A., Valenti, L.
Published in Journal of hepatology (01.04.2018)

Get full text

Journal Article

Loading…

Rare ceruloplasmin variants are associated with hyperferritinemia and increased hepatic iron in NAFLD patients: results from a NGS study

by Corradini, E., Bernardis, I., Dongiovanni, P., Buzzetti, E., Caleffi, A., Artuso, L., Pelusi, S., Tenedini, E., Tagliafico, E., Rametta, R., Fracanzani, A.L., Fargion, S., Pietrangelo, A., Valenti, L.
Published in Journal of hepatology (01.04.2018)

Get full text

Journal Article

Loading…

Tie2 Expressing Monocytes in the Spleen of Patients with Primary Myelofibrosis

by Campanelli, Rita, Fois, Gabriela, Catarsi, Paolo, Poletto, Valentina, Villani, Laura, Erba, Benedetta Gaia, Maddaluno, Luigi, Jemos, Basilio, Salmoiraghi, Silvia, Guglielmelli, Paola, Abbonante, Vittorio, Di Buduo, Christian Andrea, Balduini, Alessandra, Iurlo, Alessandra, Barosi, Giovanni, Rosti, Vittorio, Massa, Margherita
Published in PloS one (09.06.2016)

Get full text

Journal Article