Zobrazeno 1 - 10
of 342
pro vyhledávání: '"Fanale,D"'
Autor:
Bono, M., Fanale, D., Incorvaia, L., Cancelliere, D., Fiorino, A., Calò, V., Dimino, A., Filorizzo, C., Corsini, L.R., Brando, C., Madonia, G., Cucinella, A., Scalia, R., Barraco, N., Guadagni, F., Pedone, E., Badalamenti, G., Russo, A., Bazan, V.
Publikováno v:
In ESMO Open August 2021 6(4)
Autor:
Corsini, L.R., Fanale, D., Brando, C., Randazzo, U., Spinnato, V., Polizzotto, R., Russo, T.D. Bazan, Ferraro, P., Prestifilippo, O., Busuito, G., Frattallone, G.G., Gennusa, V., Perez, A., Pedone, E., Bono, M., Incorvaia, L., Badalamenti, G., Galvano, A., Russo, A., Bazan, V.
Publikováno v:
In Annals of Oncology September 2024 35 Supplement 2:S231-S231
Autor:
Fanale, D., Corsini, L.R., Randazzo, U., Brando, C., Perez, A., Russo, T.D. Bazan, Ferraro, P., Simone, A., Bono, M., Pedone, E., Piraino, P., Contino, S., Prestifilippo, O., Gennusa, V., Galvano, A., Incorvaia, L., Badalamenti, G., Iovanna, J.L., Russo, A., Bazan, V.
Publikováno v:
In Annals of Oncology September 2024 35 Supplement 2:S300-S300
Autor:
Incorvaia, L., Bazan Russo, T.D., Perez, A., Brando, C., Ferraro, P., Simone, A., Bono, M., Castellana, L., Insalaco, L., Contino, S., Gottardo, A., Gristina, V., Galvano, A., Corsini, L.R., Fanale, D., Badalamenti, G., Russo, A., Bazan, V.
Publikováno v:
In Annals of Oncology September 2024 35 Supplement 2:S955-S955
Autor:
Fanale D., Pivetti A., Cancelliere D., Spera A., Bono M., Fiorino A., Pedone E., Barraco N., Brando C., Perez A., Guarneri M. F., Russo T. D. B., Vieni S., Guarneri G., Russo A., Bazan V.
Publikováno v:
Critical Reviews in Oncology/Hematology. 172:103626
Hereditary breast and ovarian cancer syndrome is caused by germline mutations in BRCA1/2 genes. These genes are very large and their mutations are heterogeneous and scattered throughout the coding sequence. In addition to the above-mentioned mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fe85c447a0ffb9698693a8a9eda3354
https://doi.org/10.1016/j.critrevonc.2022.103626
https://doi.org/10.1016/j.critrevonc.2022.103626
Autor:
Fanale, D., Incorvaia, L., Maragliano, R., Barraco, N., Listì, A., Galvano, A., Rizzo, S., Calò, V., Corsini, L.R., Bazan, V., Russo, A.
Publikováno v:
In Annals of Oncology October 2017 28 Supplement 6:vi38-vi38
Autor:
Valentina Calò, Marta Castiglia, Viviana Bazan, Giuseppe Badalamenti, D. Cancelliere, Antonio Russo, Lorena Incorvaia, Sofia Cutaia, A. Fiorino, Nadia Barraco, Fanale D, Marco Bono, A. Pivetti
Publikováno v:
Cancers
Volume 12
Issue 5
Cancers, Vol 12, Iss 1158, p 1158 (2020)
Volume 12
Issue 5
Cancers, Vol 12, Iss 1158, p 1158 (2020)
Recent advances in the detection of germline pathogenic variants (PVs) in BRCA1/2 genes have allowed a deeper understanding of the BRCA-related cancer risk. Several studies showed a significant heterogeneity in the prevalence of PVs across different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dec893ac65145152b39fdcc499c9a53
http://hdl.handle.net/10447/431345
http://hdl.handle.net/10447/431345
Autor:
Antonio Russo, Ida De Luca, Viviana Bazan, Carlo Messina, Mimma Rizzo, Giuseppe Badalamenti, Daniel Olive, Camillo Porta, Chiara Brando, Mattia Rediti, Lorena Incorvaia, Juan L. Iovanna, Fanale D
Publikováno v:
OncoImmunology
OncoImmunology, Taylor & Francis, 2020, 9 (1), pp.1832348. ⟨10.1080/2162402X.2020.1832348⟩
Oncoimmunology
article-version (VoR) Version of Record
OncoImmunology, 2020, 9 (1), pp.1832348. ⟨10.1080/2162402X.2020.1832348⟩
OncoImmunology, Vol 9, Iss 1 (2020)
OncoImmunology, Taylor & Francis, 2020, 9 (1), pp.1832348. ⟨10.1080/2162402X.2020.1832348⟩
Oncoimmunology
article-version (VoR) Version of Record
OncoImmunology, 2020, 9 (1), pp.1832348. ⟨10.1080/2162402X.2020.1832348⟩
OncoImmunology, Vol 9, Iss 1 (2020)
Despite a proportion of renal cancer patients can experiment marked and durable responses to immune-checkpoint inhibitors, the treatment efficacy is widely variable and identifying the patient who will benefit from immunotherapy remains an issue. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4964df29d788a71130f2fc36da6bc02b
https://hal-amu.archives-ouvertes.fr/hal-03152735
https://hal-amu.archives-ouvertes.fr/hal-03152735
Autor:
Incorvaia, L., Marchetti, C., Brando, C., Perez, A., Bono, M., Barraco, N., Cancelliere, D., Pivetti, A., Cardone, F., Bazan Russo, T.D., Castellana, L., Congedo, L., Piraino, P., Ergasti, R., Gristina, V., Galvano, A., Fanale, D., Bazan, V., Scambia, G., Russo, A.
Publikováno v:
In Annals of Oncology October 2023 34 Supplement 2:S716-S716
Autor:
Lidia Rita Corsini, Marco Bono, Chiara Brando, Valentina Calò, Lorena Incorvaia, Nadia Barraco, Fanale D, A. Fiorino, Antonio Russo, Viviana Bazan, Giuseppe Badalamenti, Clarissa Filorizzo
Publikováno v:
Cancers
Volume 12
Issue 9
Cancers, Vol 12, Iss 2415, p 2415 (2020)
Volume 12
Issue 9
Cancers, Vol 12, Iss 2415, p 2415 (2020)
Simple Summary Many bilateral breast cancer patients with increased hereditary susceptibility to breast cancer result negative for BRCA1 or BRCA2 pathogenic variants and, thus, need a further genetic testing through a broader gene panel. Some patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2daedde1cb49b46f80408efcd876f1b
http://europepmc.org/articles/PMC7564956
http://europepmc.org/articles/PMC7564956