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Familial Cancer|April 13, 2022
Preimplantation genetic testing in patients with genetic susceptibility to cancerMarie-Charlotte Villy, Nelly Frydman, Céline Moutou, et al.Bulletin Du Cancer|September 26, 2020
[First results of a breast cancer risk assessment and management consultation]Catherine Uzan, Diaretou Ndiaye-Guèye, Marianne Nikpayam, et al.European Journal of Medical Genetics|November 13, 2020
Utility of a mainstreamed genetic testing pathway in breast and ovarian cancer patients during the COVID-19 pandemicPatrick R Benusiglio, Clément Korenbaum, Roseline Vibert, et al.Orphanet Journal of Rare Diseases|December 19, 2014
Renal cell tumour characteristics in patients with the Birt-Hogg-Dubé cancer susceptibility syndrome: a retrospective, multicentre studyPatrick R Benusiglio, Sophie Giraud, Sophie Deveaux, et al.Neuropathology and Applied Neurobiology|September 30, 2025
A Specific Methylation Class Identifies BAP1-Deficient Meningiomas, Including Meningeal Tumours With Poorly Differentiated Nonrhabdoid HistologyPhilippe Drabent, Mehdi Touat, Patrick R Benusiglio, et al.Gastric Cancer : Official Journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association|July 13, 2022
International Delphi consensus guidelines for follow-up after prophylactic total gastrectomy: the Life after Prophylactic Total Gastrectomy (LAP-TG) studyGeoffrey Roberts, Patrick R Benusiglio, Tanya Bisseling, et al.Gastric Cancer : Official Journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association|December 6, 2018
Clinical implications of CTNNA1 germline mutations in asymptomatic carriersPatrick R Benusiglio, Chrystelle Colas, Erell Guillerm, et al.Journal of Medical Genetics|May 28, 2013
CDH1 germline mutations and the hereditary diffuse gastric and lobular breast cancer syndrome: a multicentre studyPatrick R Benusiglio, David Malka, Etienne Rouleau, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|May 28, 2015
Revisiting Li-Fraumeni Syndrome From TP53 Mutation CarriersGaëlle Bougeard, Mariette Renaux-Petel, Jean-Michel Flaman, et al.European Journal of Medical Genetics|November 21, 2025
French recommendations on multi-gene panel testing in renal cell carcinomaSophie Giraud, Pascaline Berthet, Caroline Abadie, et al.Pageof 5