Zobrazeno 1 - 10
of 37
pro vyhledávání: '"A. C. Nero"'
Autor:
A. Di Pilla, C. Nero, M. L. Specchia, F. Ciccarone, L. Boldrini, J. Lenkowicz, B. Alberghetti, A. Fagotti, A. C. Testa, V. Valentini, E. Sala, G. Scambia
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-8 (2024)
Abstract Current approach to identify BRCA 1/2 carriers in the general population is ineffective as most of the carriers remain undiagnosed. Radiomics is an emerging tool for large scale quantitative analysis of features from standard diagnostic imag
Externí odkaz:
https://doaj.org/article/8976b967038b4974879d560ffed360a3
Autor:
Caterina P Minniti, Henny H. Billett, Daniel McMahon, Modupe Idowu, Nirmish Shah, Richard A. Drachtman, Archana Sharma, Alexander Glaros, Maureen Okam Okam Achebe, Alecia C Nero, Susanna Curtis, Biree Andemariam
Publikováno v:
Blood. 140:8276-8277
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d9863a6d11e103429f50f0909be8959
https://doi.org/10.1182/blood-2022-169334
https://doi.org/10.1182/blood-2022-169334
Autor:
E. Giudice, V. Ghizzoni, M.V. Carbone, S. Cappuccio, V. Salutari, L. Musacchio, C. Nero, C. Ricci, F. Camarda, M.T. Perri, D. Giannarelli, A. Fagotti, G. Scambia, D. Lorusso
Publikováno v:
Annals of Oncology. 33:S1424-S1425
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5011eaa3b5bf2c29acc65a2b3fae6321
https://doi.org/10.1016/j.annonc.2022.09.133
https://doi.org/10.1016/j.annonc.2022.09.133
Autor:
E. Giudice, V. Ghizzoni, M.V. Carbone, V. Salutari, S. Cappuccio, C. Nero, L. Musacchio, C. Ricci, F. Ciccarone, F. Camarda, M.T. Perri, D. Giannarelli, F. Fanfani, G. Scambia, D. Lorusso
Publikováno v:
Annals of Oncology. 33:S1392
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b51c04888eb542919d9d7618e11e892b
https://doi.org/10.1016/j.annonc.2022.09.028
https://doi.org/10.1016/j.annonc.2022.09.028
Autor:
Deva Sharma, Russell E. Ware, Michael J. Paidas, Lydia H. Pecker, Alecia C. Nero, Andra H. James, Kim Smith-Whitley
Publikováno v:
Br J Haematol
There is an immediate need to address long-standing questions about the reproductive health of girls and women with sickle cell disease (SCD). There are many SCD-related reproductive risks and uncertainties across girls' and women's reproductive life
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e53a360449a749446b8375163cc81d6
https://europepmc.org/articles/PMC8448913/
https://europepmc.org/articles/PMC8448913/
Autor:
Raffaella Colombatti, Alecia C. Nero, Erfan Nur, Cassandra Trimnell, John R. James, Olivera Rajkovic-Hooley, Tom Bailey, Jean-Benoît Arlet, Mariane de Montalembert, Ifeyinwa Osunkwo, Caterina P. Minniti, Suman Jain, Miguel R. Abboud, Fuad El Rassi, Beverley Francis-Gibson, Wasil Jastaniah, Biree Andemariam, Nicholas Ramscar, Marimilia Pita, Baba Inusa
Publikováno v:
Blood. 136:8-10
Background: SWAY was a cross-sectional survey that assessed the global impact and treatment of sickle cell disease (SCD) (James et al. ASH 2019). SCD puts patients at risk of multiple complications driven by vaso-occlusion and hemolytic anemia. Vaso-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74b4c4b0a2213b89defe37bb12ccb0db
https://doi.org/10.1182/blood-2020-137103
https://doi.org/10.1182/blood-2020-137103
Autor:
Tom Bailey, Jean-Benoît Arlet, Beverley Francis-Gibson, Baba Inusa, Caterina P. Minniti, John R. James, Alecia C. Nero, Olivera Rajkovic-Hooley, Raffaella Colombatti, Biree Andemariam, Cassandra Trimnell, Fuad El Rassi, Erfan Nur, Miguel R. Abboud, Nicholas Ramscar, Mariane de Montalembert, Marimilia Pita, Wasil Jastaniah, Ifeyinwa Osunkwo, Suman Jain
Publikováno v:
Blood. 136:3-5
Background: Sickle cell disease (SCD) is associated with many clinical complications, with vaso-occlusive crises (VOCs) being a hallmark of the disease. SCD-related complications are largely driven by vaso-occlusion and hemolytic anemia, and can lead
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2bfd823ce6a2378e59a7753b21a693bd
https://doi.org/10.1182/blood-2020-136073
https://doi.org/10.1182/blood-2020-136073
Autor:
G. Scambia, V. Salutari, L. Musacchio, S. Siena, S. Pignata, L. Zavallone, G. Valabrega, G. Cormio, A.M. Mosconi, C. Ricci, V. Ghizzoni, M.V. Carbone, E. Giudice, F. Camarda, C. Nero, F. Tronconi, D. Lorusso
Publikováno v:
Annals of Oncology. 33:S401
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12df5ee6e2c9e586f693a6bd6b02d82b
https://doi.org/10.1016/j.annonc.2022.04.063
https://doi.org/10.1016/j.annonc.2022.04.063
Autor:
Olivera Rajkovic-Hooley, Suman Jain, Mariane de Montalembert, Biree Andemariam, Ifeyinwa Osunkwo, Fuad El Rassi, Laurie DeBonnett, Nicholas Ramscar, Alecia C. Nero, Tom Bailey, Baba Inusa, Jean Benoit Arlet, Caterina P. Minniti, Miguel R. Abboud, John R. James, Raffaella Colombatti, Marimilia Pita, Wasil Jastaniah, Erfan Nur, Beverley Francis-Gibson, Cassandra Trimnell
Publikováno v:
American journal of hematology, 96(4), 404-417. Wiley-Liss Inc.
American Journal of Hematology
American Journal of Hematology
Sickle cell disease (SCD) is a genetic disorder, characterized by hemolytic anemia and vaso‐occlusive crises (VOCs). Data on the global SCD impact on quality of life (QoL) from the patient viewpoint are limited. The international Sickle Cell World
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66b76675bc2ae4e1ba064e55d1b77bcf
https://pubmed.ncbi.nlm.nih.gov/33393092
https://pubmed.ncbi.nlm.nih.gov/33393092
Autor:
Alecia C. Nero, John R. James, Jean-Benoît Arlet, Biree Andemariam, Caterina P. Minniti, Cassandra Trimnell, Ifeyinwa Osunkwo, Wasil Jastaniah, Fuad El Rassi, Raffaella Colombatti, Laurie DeBonnett, Miguel R. Abboud, Beverley Francis-Gibson, Marimilia Pita, Tom Bailey, Olivera Rajkovic-Hooley, Baba Inusa, Erfan Nur, Mariane de Montalembert, Suman Jain
Publikováno v:
Blood. 138:3026-3026
Background: SCD is an inherited blood disorder that for many patients (pts) has a high clinical burden, results in poor quality of life (QoL), and reduces life expectancy. Gaining a deeper understanding of pt and HCP experiences of SCD is important t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf711241c9bd9816d3f4dbefc2d41a51
https://doi.org/10.1182/blood-2021-145409
https://doi.org/10.1182/blood-2021-145409