Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Fernanda Cunha Capareli"'
Gastrointestinal stromal tumors: advances in molecular characterization and therapeutic implications
Autor:
Nildevande Firmino Lima-Jr, Marcello Moro Queiroz, Julia Sousa Leal Franco, Domingos Savio do Rego Lins-Junior, Eduardo Felício de Campos, Beatriz Mendes Awni, Luiz Guilherme Cernaglia Aureliano de Lima, Frederico Teixeira, Fábio de Oliveira Ferreira, Eduardo Hiroshi Akaishi, Fernanda Cunha Capareli, Rodrigo Ramella Munhoz
Publikováno v:
Brazilian Journal of Oncology, Vol 20 (2024)
Recognition of the molecular basis of gastrointestinal stromal tumors has paved the way for significant breakthroughs in the diagnosis and treatment of this disease as well as positioned gastrointestinal stromal tumors as a framework for the concept
Externí odkaz:
https://doaj.org/article/7b4c4e8796894a1da09e29d39411e70c
Autor:
Marcello Moro Queiroz, Carlos Diego Holanda Lopes, Alessandra Corte Real Salgues, Felipe de Galiza Barbosa, Emerson Shigueaki Abe, Thales Parenti Silveira, Marcel Cerqueira Cesar Machado, Fernanda Cunha Capareli
Publikováno v:
European Journal of Hybrid Imaging, Vol 5, Iss 1, Pp 1-6 (2021)
Abstract Background Pancreatic neuroendocrine tumor (PNET) is a subgroup of neuroendocrine tumor (NET) that has unique biology and natural history. The histological classification has a major role in the management of this pathology, but in recent ye
Externí odkaz:
https://doaj.org/article/b8f9e536c68d4cecaf600060f9a3103f
Autor:
Marco Gerlinger, Alice Newey, Paulo M. Hoff, Anamaria A. Camargo, Franciele Hinterholz Knebel, Jorge Sabbaga, Dimitrios Kleftogiannis, Frederico Costa, Beatrice Griffiths, Louise J. Barber, Maurício Fernando Silva Almeida Ribeiro, Fabiana Bettoni, Kerry Fenwick, Fernanda Cunha Capareli, Andrew Woolston, Leonardo da Fonseca
Publikováno v:
Cancers, Vol 12, Iss 3736, p 3736 (2020)
Cancers
Volume 12
Issue 12
Cancers
Volume 12
Issue 12
Simple Summary Recent studies have shown the potential of next generation sequencing (NGS) for the identification of genetic variants in tumour DNA that has been released into the bloodstream (ctDNA). However, such variants are often rare in the samp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7a954ebec754376ae94443cc8a7f8da
https://www.mdpi.com/2072-6694/12/12/3736
https://www.mdpi.com/2072-6694/12/12/3736