Detalhe da pesquisa
1.
AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer.
Genes Chromosomes Cancer
; 62(4): 210-222, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36502525
2.
Comprehensive study of nine novel cases of TFEB-amplified renal cell carcinoma: an aggressive tumour with frequent PDL1 expression.
Histopathology
; 81(2): 228-238, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35562857
3.
MSH2 c.1022T>C, p.Leu341Pro is a founder pathogenic variation and a major cause of Lynch syndrome in the North of France.
Genes Chromosomes Cancer
; 59(2): 111-118, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31433521
4.
Complete pathological response following chemotherapy and radiotherapy in two cases of advanced anaplastic thyroid carcinoma.
Eur Thyroid J
; 12(1)2023 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36377723
5.
Diagnosis of Lynch Syndrome and Strategies to Distinguish Lynch-Related Tumors from Sporadic MSI/dMMR Tumors.
Cancers (Basel)
; 13(3)2021 Jan 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-33530449