Detalhe da pesquisa
1.
Recommendations for the use of next-generation sequencing (NGS) for patients with advanced cancer in 2024: a report from the ESMO Precision Medicine Working Group.
Ann Oncol
; 2024 May 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38834388
2.
The role of skin tests with polyethylene glycol and polysorbate 80 in the vaccination campaign for COVID-19: results from an Italian multicenter survey.
Eur Ann Allergy Clin Immunol
; 56(1): 17-25, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36927838
3.
ESMO recommendations on the standard methods to detect RET fusions and mutations in daily practice and clinical research.
Ann Oncol
; 32(3): 337-350, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33455880
4.
Sensitization to Gibberellin-Regulated Protein (Peamaclein) Among Italian Cypress Pollen-Sensitized Patients.
J Investig Allergol Clin Immunol
; 32(1): 40-47, 2021 02 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32732184
5.
Recommendations for the use of next-generation sequencing (NGS) for patients with metastatic cancers: a report from the ESMO Precision Medicine Working Group.
Ann Oncol
; 31(11): 1491-1505, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32853681
6.
Acinic cell carcinoma of the parotid gland: from pathogenesis to management: a literature review.
Eur Arch Otorhinolaryngol
; 277(10): 2673-2679, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32367151
7.
ESMO recommendations on microsatellite instability testing for immunotherapy in cancer, and its relationship with PD-1/PD-L1 expression and tumour mutational burden: a systematic review-based approach.
Ann Oncol
; 30(8): 1232-1243, 2019 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31056702
8.
Transcriptomic analysis and mutational status of IDH1 in paired primary-recurrent intrahepatic cholangiocarcinoma.
BMC Genomics
; 19(1): 440, 2018 Jun 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29871612
9.
The European Society for Medical Oncology (ESMO) Precision Medicine Glossary.
Ann Oncol
; 29(1): 30-35, 2018 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29140430
10.
Adipocytes sustain pancreatic cancer progression through a non-canonical WNT paracrine network inducing ROR2 nuclear shuttling.
Int J Obes (Lond)
; 42(3): 334-343, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29151594
11.
Carbon dating cancer: defining the chronology of metastatic progression in colorectal cancer.
Ann Oncol
; 28(6): 1243-1249, 2017 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28327965
12.
A systems approach identifies time-dependent associations of multimorbidities with pancreatic cancer risk.
Ann Oncol
; 28(7): 1618-1624, 2017 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28383714
13.
Prognostic impact and implications of extracapsular lymph node involvement in colorectal cancer: a systematic review with meta-analysis.
Ann Oncol
; 27(1): 42-8, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26483050
14.
ALK gene copy number gains in non-small-cell lung cancer: prognostic impact and clinico-pathological correlations.
Respir Res
; 17(1): 105, 2016 08 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-27561692
15.
Molecular biology of neuroendocrine tumors: from pathways to biomarkers and targets.
Cancer Metastasis Rev
; 33(1): 345-51, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24375391
16.
Key role of dual specificity kinase TTK in proliferation and survival of pancreatic cancer cells.
Br J Cancer
; 111(9): 1780-7, 2014 Oct 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-25137017
17.
Angiogenic and signalling proteins correlate with sensitivity to sequential treatment in renal cell cancer.
Br J Cancer
; 109(3): 686-93, 2013 Aug 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-23839492
18.
A clinical-biological risk stratification model for resected gastric cancer: prognostic impact of Her2, Fhit, and APC expression status.
Ann Oncol
; 24(3): 693-701, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23131390
19.
Hymenoptera Venom Immunotherapy: How to Safely Switch to the Same Venom From a Different Manufacturer.
J Investig Allergol Clin Immunol
; 28(3): 205-208, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29939145
20.
Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.
Nat Genet
; 13(2): 214-8, 1996 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-8640229