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European Journal of Cancer (Oxford, England : 1990)|April 27, 2020
Direct-to-consumer misleading information on cancer risks calls for an urgent clarification of health genetic testing performed by commercial companiesAntoine de Pauw, Mathias Schwartz, Chrystelle Colas, et al.
Breast (Edinburgh, Scotland)|March 2, 2019
"Decoding hereditary breast cancer" benefits and questions from multigene panel testingChrystelle Colas, Lisa Golmard, Antoine de Pauw, et al.
European Journal of Human Genetics : EJHG|January 29, 2026
Results of a multigene panel testing approach targeting patients with suspected genetic predisposition to pancreatic ductal adenocarcinomaBruno Buecher, Mathilde Warcoin, Emilie Rolland, et al.
Frontiers in Oncology|August 2, 2024
Major response of a peritoneal mesothelioma to nivolumab and ipilimumab: a case report, molecular analysis and review of literatureMarie-Florence Reveneau, Julien Masliah-Planchon, Manuel Fernandez, et al.
Pharmacological Research|August 25, 2018
A PK/PD study of Delta-4 abiraterone metabolite in metastatic castration-resistant prostate cancer patientsBenoit Blanchet, Edith Carton, Mohammad Alyamani, et al.
European Journal of Medical Genetics|August 23, 2021
Cancer predisposition and germline CTNNA1 variantsSilvana Lobo, Patrick R Benusiglio, Florence Coulet, et al.
Hereditary Cancer in Clinical Practice|June 21, 2012
Prevalance of BRCA1 and BRCA2 mutations in familial breast cancer patients in LebanonNadine Jalkh, Jinane Nassar-Slaba, Eliane Chouery, et al.
Familial Cancer|January 21, 2015
Germline RAD51B truncating mutation in a family with cutaneous melanomaKarin A W Wadt, Lauren G Aoude, Lisa Golmard, et al.
Familial Cancer|August 19, 2017
Sporadic endometrial adenocarcinoma with MMR deficiency due to biallelic MSH2 somatic mutationsBruno Buecher, Antoine De Pauw, Louis Bazire, et al.
Pediatric Blood & Cancer|February 23, 2018
Mutiple DICER1-related lesions associated with a germline deep intronic mutationFlorian Verrier, Catherine Dubois d'Enghien, Marion Gauthier-Villars, et al.
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