Detalhe da pesquisa
1.
Genome-wide profiling of non-smoking-related lung cancer cells reveals common RB1 rearrangements associated with histopathologic transformation in EGFR-mutant tumors.
Ann Oncol
; 31(2): 274-282, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31959344
2.
Psychological impact of multigene cancer panel testing in patients with a clinical suspicion of hereditary cancer across Spain.
Psychooncology
; 27(6): 1530-1537, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29498768
3.
Identification of a founder BRCA1 mutation in the Moroccan population.
Clin Genet
; 90(4): 361-5, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-26864382
4.
Pazopanib in pretreated advanced neuroendocrine tumors: a phase II, open-label trial of the Spanish Task Force Group for Neuroendocrine Tumors (GETNE).
Ann Oncol
; 26(9): 1987-1993, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26063633
5.
Molecular profiling and feasibility using a comprehensive hybrid capture panel on a consecutive series of non-small-cell lung cancer patients from a single centre.
ESMO Open
; 8(6): 102197, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-38070435
6.
Durvalumab plus tremelimumab for the treatment of advanced neuroendocrine neoplasms of gastroenteropancreatic and lung origin.
Nat Commun
; 14(1): 2973, 2023 05 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-37221181
7.
Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2.
Br J Cancer
; 104(8): 1356-61, 2011 Apr 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-21427728
8.
Germline ATM mutational analysis in BRCA1/BRCA2 negative hereditary breast cancer families by MALDI-TOF mass spectrometry.
Breast Cancer Res Treat
; 128(2): 573-9, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21445571
9.
Incidence, patterns of care and prognostic factors for outcome of gastroenteropancreatic neuroendocrine tumors (GEP-NETs): results from the National Cancer Registry of Spain (RGETNE).
Ann Oncol
; 21(9): 1794-1803, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20139156
10.
Founder effect of a pathogenic MSH2 mutation identified in Spanish families with Lynch syndrome.
Clin Genet
; 78(2): 186-90, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20095990
11.
BRCA1 5272-1G>A and BRCA2 5374delTATG are founder mutations of high relevance for genetic counselling in breast/ovarian cancer families of Spanish origin.
Clin Genet
; 77(1): 60-9, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19912264
12.
Clinical guideline seom: hereditary colorectal cancer.
Clin Transl Oncol
; 17(12): 962-71, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26586118
13.
SEOM clinical guidelines in Hereditary Breast and ovarian cancer.
Clin Transl Oncol
; 17(12): 956-61, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26669313
14.
SEOM clinical guidelines for the diagnosis and treatment of gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs) 2014.
Clin Transl Oncol
; 16(12): 1025-34, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25183048