Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers

Autor: Mavaddat, N., Antoniou, A.C., Mooij, T.M., Hooning, M.J., Heemskerk-Gerritsen, B.A., Nogues, C., Laborde, L., Breysse, E., Stoppa-Lyonnet, D., Gauthier-Villars, M., Buecher, B., Caron, O., Fourme-Mouret, E., Fricker, J.P., Lasset, C., Bonadona, V., Berthet, P., Faivre, L., Luporsi, E., Mari, V., Gladieff, L., Gesta, P., Sobol, H., Eisinger, F., Longy, M., Dugast, C., Colas, C., Coupier, I., Pujol, P., Corsini, C., Lortholary, A., Vennin, P., Adenis, C., Nguyen, T.D., Delnatte, C., Tinat, J., Tennevet, I., Limacher, J.M., Maugard, C., Bignon, Y.J., Demange, L., Penet, C., Dreyfus, H., Cohen-Haguenauer, O., Venat-Bouvet, L., Leroux, D., Zattara-Cannoni, H., Fert-Ferrer, S., Bera, O., Ellis, S., Barrowdale, D., Frost, D., Evans, D.G., Izatt, L., Adlard, J., Eeles, R., Brewer, C., Tischkowitz, M., Henderson, A., Cook, J., Eccles, D., Hogervorst, F.B.L., Collee, J.M., Asperen, C.J. van, Mensenkamp, A.R., Ausems, M.G.E.M., Meijers-Heijboer, H.E.J., Engelen, K. van, Blok, M.J., Oosterwijk, J.C., Verloop, J., Broek, E. van den, Mourits, M.J.E., Koppert, L.B., Hopper, J.L., John, E.M., Chung, W.K., Andrulis, I.L., Daly, M.B., Buys, S.S., Benitez, J., Caldes, T., Jakubowska, A., Simard, J., Singer, C.F., Tan, Y., Olah, E., Navratilova, M., Foretova, L., Gerdes, A.M., Roos-Blom, M.J., Leeuwen, F.E. van, Arver, B., Olsson, H., Schmutzler, R.K., Engel, C., Kast, K., Phillips, K.A., Terry, M.B., Milne, R.L., Goldgar, D.E., Rookus, M.A., Andrieu, N., Easton, D.F., GENEPSO, EMBRACE, HEBON, kConFab Investigators, IBCCS, kConFab, BCFR

Publikováno v: Breast Cancer Research
Breast Cancer Research, 2020, 22 (1), pp.8. ⟨10.1186/s13058-020-1247-4⟩
Breast Cancer Research, 22(1):8. BioMed Central
Breast Cancer Research, BioMed Central, 2020, 22 (1), pp.8. ⟨10.1186/s13058-020-1247-4⟩
Breast Cancer Research, 22(1):8. BioMed Central Ltd.
Breast Cancer Research, 22, 1
HEBON 2020, ' Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk : An international prospective cohort of BRCA1 and BRCA2 mutation carriers ', Breast Cancer Research, vol. 22, no. 1, 8 . https://doi.org/10.1186/s13058-020-1247-4
Repisalud
Instituto de Salud Carlos III (ISCIII)
Breast cancer research, 22(1):8. BioMed Central Ltd.
Evans, D G & et al. 2020, ' Risk-reducing salpingo-oophorectomy, natural menopause and breast cancer risk : an international prospective cohort of BRCA1 and BRCA2 mutation carriers ', Breast Cancer Research . https://doi.org/10.1186/s13058-020-1247-4
Breast Cancer Research : BCR
Breast cancer research, 22(1):8. BioMed Central
Breast Cancer Research, 22
Breast Cancer Research, 22(1):8. BioMed Central Ltd
Breast Cancer Research, 22(1). BMC
Mavaddat, N, Antoniou, A C, Mooij, T M, Hooning, M J, Heemskerk-Gerritsen, B A, Noguès, C, Gauthier-Villars, M, Caron, O, Gesta, P, Pujol, P, Lortholary, A, Barrowdale, D, Frost, D, Evans, D G, Izatt, L, Adlard, J, Eeles, R, Brewer, C, Tischkowitz, M, Henderson, A, Cook, J, Eccles, D, van Engelen, K, Mourits, M J E, Ausems, M G E M, Koppert, L B, Hopper, J L, John, E M, Chung, W K, Andrulis, I L, Daly, M B, Buys, S S, Benitez, J, Caldes, T, Jakubowska, A, Simard, J, Singer, C F, Tan, Y, Olah, E, Navratilova, M, Foretova, L, Gerdes, A-M, Roos-Blom, M-J, Van Leeuwen, F E, Arver, B, Olsson, H, Schmutzler, R K, Engel, C, Kast, K, Phillips, K-A & GENEPSO 2020, ' Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk : an international prospective cohort of BRCA1 and BRCA2 mutation carriers ', Breast Cancer Research, vol. 22, no. 1, 8 . https://doi.org/10.1186/s13058-020-1247-4
Breast Cancer Research, Vol 22, Iss 1, Pp 1-11 (2020)

The effect of risk-reducing salpingo-oophorectomy (RRSO) on breast cancer risk for BRCA1 and BRCA2 mutation carriers is uncertain. Retrospective analyses have suggested a protective effect but may be substantially biased. Prospective studies have had

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::897204daf2b6489f47952598d573c042
https://www.hal.inserm.fr/inserm-02445596

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Diagnosis of Constitutional Mismatch Repair-deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents

Autor: Bodo, S., Colas, C., Buhard, O., Collura, A., Tinat, J., Lavoine, N., Guilloux, A., Chalastanis, A., Lafitte, P., Coulet, F., Buisine, M.P., Ilencikova, D., Ruiz-Ponte, C., Kinzel, M., Grandjouan, S., Brems, H.I., Lejeune, S., Blanche, H., Wang, Q., Caron, O., Cabaret, O., Syrcek, M.L., Vidaud, D., Parfait, B., Verloes, A., Knappe, U.J., Soubrier, F., Mortemousque, I., Leis, A., Auclair-Perrossier, J., Frebourg, T., Flejou, J.F., Entz-Werle, N., Leclerc, J., Malka, D., Cohen-Haguenauer, O., Goldberg, Y., Gerdes, A.M., Fedhila, F., Mathieu-Dramard, M., Lin, R.H., Wafaa, B., Gauthier-Villars, M., Bourdeaut, F., Sheridan, E., Vasen, H., Brugieres, L., Wimmer, K., Muleris, M., Duva, A., European Consortium Care CMMRD

Publikováno v: RUNA. Repositorio da Consellería de Sanidade e Sergas
Servizo Galego de Saúde (SERGAS)

Background & Aims Patients with bi-allelic germline mutations in mismatch repair (MMR) genes ( MLH1 , MSH2 , MSH6 , or PMS2 ) develop a rare but severe variant of Lynch syndrome called constitutional MMR deficiency (CMMRD). This syndrome is character

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c1efb9499e981c6474fa6b3f83f81a7
https://lirias.kuleuven.be/handle/123456789/501985

Les espoirs de la thérapie génique

Autor: Cohen Haguenauer O., BORDIGNON , CLAUDIO

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_____10495::46fd19ffb6f5101082c2d9eb91697c60

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