Zobrazeno 1 - 10
of 387
pro vyhledávání: '"Donti, E."'
Autor:
Floridia, G., Falbo, V., Censi, F., Tosto, F., Salvatore, M., Baroncini, A., Battaglia, P., Conti, A., Donti, E., La Starza, R., Nitsch, L., Pierluigi, M., Piombo, G., Susca, F., Mancini, M., Mecucci, C., Calzolari, E., Bricarelli, F. Dagna, Guanti, G., Taruscio, D.
Publikováno v:
Community Genetics, 2008 Jan 01. 11(5), 295-303.
Externí odkaz:
https://www.jstor.org/stable/26679675
Autor:
Zaccaria, A, Testoni, N, Valenti, Am, Luatti, S, Tonelli, M, Marzocchi, G, Cipriani, R, Baldazzi, C, Giannini, B, Stacchini, M, Gamberini, C, Castagnetti, F, Rosti, G, Azzena, A, Cavazzini, Francesco, Cianciulli, Am, Dalsass, A, Donti, E, Giugliano, E, Gozzetti, A, Grimoldi, Mg, Ronconi, S, Santoro, A, Spedicato, F, Zanatta, L, Baccarani, M, GIMEMA Working Party on, C. M. L.
Additional chromosome abnormalities (ACAs) occur in less than 10% of cases at diagnosis of Philadelphia chromosome (Ph)-positive chronic myelogenous leukemia (CML). In some cases, on the basis of the persistence of the ACAs in Ph-negative cells after
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::532b58a4912c9e64d64394c36699fbbf
http://hdl.handle.net/11391/616897
http://hdl.handle.net/11391/616897
Autor:
Giardino, D, Corti, C, Ballarati, L, Colombo, D, Sala, E, Villa, N, Piombo, G, Pierluigi, M, Faravelli, F, Guerneri, S, Coviello, D, Lalatta, F, Cavallari, U, Bellotti, D, Barlati, Sergio, Croci, G, Franchi, F, Savin, E, Nocera, G, Amico, Fp, Granata, P, Casalone, R, Nutini, L, Lisi, E, Torricelli, F, Giussani, U, Facchinetti, B, Guanti, G, DI GIACOMO, M, Susca, Fp, Pecile, V, Romitti, L, Cardarelli, L, Racalbuto, E, Police, Ma, Chiodo, F, Rodeschini, O, Falcone, P, Donti, E, Grimoldi, Mg, Martinoli, E, Stioui, S, Caufin, D, Lauricella, Sa, Tanzariello, Sa, Voglino, G, Lenzini, E, Besozzi, M, Larizza, L, Dalprà, L.
Publikováno v:
Prenatal diagnosis. 29(3)
OBJECTIVE: We surveyed the datasheets of 29 laboratories concerning prenatal diagnosis of de novo apparently balanced chromosome rearrangements to assess the involvement of specific chromosomes, the breakpoints distribution and the impact on the preg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::928949598bb92b2c3badcd58f2aab413
https://pubmed.ncbi.nlm.nih.gov/19248039
https://pubmed.ncbi.nlm.nih.gov/19248039
Autor:
Castrioto, A, Prontera, P, DI GREGORIO, Eleonora, Rossi, V, Parnetti, L, Rossi, A, Donti, E, Brusco, Alfredo, Calabresi, P, Tambasco, N.
SCA15 is a recently identified spinocerebellar ataxia with pure cerebellar involvement. Here, we report a novel SCA15 Italian family with atypical clinical features.Three affected members from a three-generation family segregating an autosomal domina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::af0864e2671c35c5d2a040df7fb01f40
http://hdl.handle.net/11391/616097
http://hdl.handle.net/11391/616097
Autor:
Corre, T1, Schuettler, J, Bione, S, Marozzi, A, Persani, L, Rossetti, R, Torricelli, F, Giotti, I, Vogt, P, Toniolo, D, Biondi, M, Bruni, V, Brigante, C, Cisternino, M, Colombo, I, Crosignani, Pg, D'Avanzo, Mg, Dalprà, L, Danesino, C, Di Prospero, F, Donti, E, Falorni, Alberto, Fusi, F, Lanzi, R, Larizza, D, Locatelli, N, Madaschi, S, Maghnie, M, Marzotti, S, Migone, N, Nappi, R, Palli, D, Patricelli, Mg, Pisani, C, Prontera, P, Petraglia, F, Renieri, A, Ricca, I, Ripamonti, A, Russo, G, Russo, S, Tibiletti, Mg, Tonacchera, M, Vegetti, W, Villa, N, Vineis, P, Zuffardi, O.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3982::d0efb0d9ae141af113a69a3e6c2875df
http://hdl.handle.net/11391/1214692
http://hdl.handle.net/11391/1214692
Autor:
Zaccaria, A., Testoni, N., Valenti, A. M., Luatti, S., Tonelli, M., Marzocchi, G., Cipriani, R., Baldazzi, C., Giannini, B., Stacchini, M., Gamberini, C., Castagnetti, F., Rosti, G., Azzena, A., Bernardi, F., Cavazzini, Francesco, Cianciulli, A., Dalsass, A., Donti, E., Giugliano, E., Gozzetti, A., Grimoldi, M. G., Manna, M., Modaferri, B., Piovani, G., Ronconi, S., Santoro, A., Santulli, B., Spedicato, F., Zanatta, L., on behalf of the GIMEMA WP on CML, Baccarani M.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3709::a7234e1c3b950fb2533c78aac7b2473a
http://hdl.handle.net/11392/1401588
http://hdl.handle.net/11392/1401588
Autor:
Corre, T., Schuettler, J., Bione, S., Marozzi, A., Persani, L., Rossetti, R., Torricelli, F., Giotti, I., Vogt, P., Toniolo, D., Italian Network for the study of Ovarian Dysfunctions, Biondi, M, Bruni, V, Brigante, C, Cisternino, M, Colombo, I, Crosignani, Pg, D'Avanzo, Mg, Dalprà, L, Danesino, C, Di Prospero, F, Donti, E, Falorni, A, Fusi, F, Lanzi, R, Larizza, D, Locatelli, N, Madaschi, S, Maghnie, M, Marzotti, S, Migone, N, Nappi, R, Palli, D, Patricelli, Mg, Pisani, C, Prontera, P, Petraglia, F, Renieri, Alessandra, Ricca, I, Ripamonti, A, Russo, G, Russo, S, Tibiletti, Mg, Tonacchera, M, Vegetti, W, Villa, N, Vineis, P, Zuffardi, O.
Background Three variants of the human INHA gene have been reported to be associated with premature ovarian failure (POF) in case-control studies involving a small number of patients and controls. Since inhibin has a fundamental role in the control o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90256ec1fee85d5e4ffeae467493aa7b
http://hdl.handle.net/11365/23962
http://hdl.handle.net/11365/23962
Autor:
Prontera, P., Ferrando, B., Giuliani, V., Falcinelli, F., Mencarelli, A., Rogaia, D., Barbara Pasini, Donti, E.
Publikováno v:
Scopus-Elsevier
Familial paragangliomas/pheochromocytomas are dominantly inherited disorders characterized by the development of highly vascularized tumors of the head and neck, derived from non-chromaffin cells of the extra-adrenal paraganglia, and tumors with endo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::657d33e0dba4b9518d71e8b3634f8791
http://hdl.handle.net/11391/151467
http://hdl.handle.net/11391/151467