Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Neoplastic Syndromes, Hereditary / diagnosis"'
Autor:
Jiil, Chung, Logine, Negm, Vanessa, Bianchi, Lucie, Stengs, Anirban, Das, Zhihui Amy, Liu, Sumedha, Sudhaman, Melyssa, Aronson, Ledia, Brunga, Melissa, Edwards, Victoria, Forster, Martin, Komosa, Scott, Davidson, Jodi, Lees, Patrick, Tomboc, David, Samuel, Roula, Farah, Anne, Bendel, Jeffrey, Knipstein, Kami Wolfe, Schneider, Agnes, Reschke, Shayna, Zelcer, Alexandra, Zorzi, Robert, McWilliams, William D, Foulkes, Raymond, Bedgood, Lindsay, Peterson, Sara, Rhode, An, Van Damme, Isabelle, Scheers, Sharon, Gardner, Gabriel, Robbins, Magimairajan Issai, Vanan, M Stephen, Meyn, Rebecca, Auer, Brandie, Leach, Carol, Burke, Anita, Villani, David, Malkin, Eric, Bouffet, Annie, Huang, Michael D, Taylor, Carol, Durno, Adam, Shlien, Cynthia, Hawkins, Gad, Getz, Yosef E, Maruvka, Uri, Tabori
Publikováno v:
Journal of Clinical Oncology, (2022)
Journal of Clinical Oncology, Vol. 41, no.4, p. 766-777 (2023)
Journal of Clinical Oncology, Vol. 41, no.4, p. 766-777 (2023)
PURPOSE Diagnosis of Mismatch Repair Deficiency (MMRD) is crucial for tumor management and early detection in patients with the cancer predisposition syndrome constitutional mismatch repair deficiency (CMMRD). Current diagnostic tools are cumbersome
Autor:
Anne Marie Jelsig, Niels Jespersen, John Gásdal Karstensen, Zohreh Ketabi, Karina Rønlund, Lone Ena Munk Sunde, Ole Thorlacius-Ussing, Wadt, Karin A. W., Niels Qvist, Charlotte Kvist Lautrup
Publikováno v:
Jelsig, A M, Jespersen, N, Karstensen, J G, Ketabi, Z, Rønlund, K, Sund, L, Thorlacius-Ussing, O, Wadt, K, Qvist, N & Lautrup, C K 2022, ' Nye arvelige polyposesyndromer som differentialdiagnose hos patienten med tarmpolypper ', Ugeskrift for Laeger, bind 2022, nr. 6, V02210148 . < https://ugeskriftet.dk/videnskab/nye-arvelige-polyposesyndromer-som-differentialdiagnose-hos-patienten-med-tarmpolypper >
Aalborg University
Jelsig, A M, Jespersen, N, Karstensen, J G, Ketabi, Z, Rønlund, K, Sunde, L E M, Thorlacius-Ussing, O, Wadt, K A W, Qvist, N & Lautrup, C K 2021, ' Nye arvelige polyposesyndromer som differentialdiagnose hos patienten med tarmpolypper ', Ugeskrift for Laeger, bind 183, V02210148 . < https://ugeskriftet-dk.auh.aub.aau.dk/videnskab/nye-arvelige-polyposesyndromer-som-differentialdiagnose-hos-patienten-med-tarmpolypper >
Jelsig, A M, Jespersen, N, Karstensen, J G, Ketabi, Z, Rønlund, K, Sunde, L, Thorlacius-Ussing, O, Wadt, K, Qvist, N & Lautrup, C K 2021, ' Nye arvelige polyposesyndromer som differentialdiagnose hos patienten med tarmpolypper ', Ugeskrift for Laeger, bind 183, nr. 38, :V02210148 . < https://content.ugeskriftet.dk/sites/default/files/scientific_article_files/2022-03/v02210148_web.pdf >
Jelsig, A M, Jespersen, N, Karstensen, J G, Ketabi, Z, Rønlund, K, Sund, L, Thorlacius-Ussing, O, Wadt, K, Qvist, N & Lautrup, C K 2021, ' Nye arvelige polyposesyndromer som differentialdiagnose hos patienten med tarmpolypper ', Ugeskrift for Læger, bind 183, nr. 38 . < https://ugeskriftet.dk/videnskab/nye-arvelige-polyposesyndromer-som-differentialdiagnose-hos-patienten-med-tarmpolypper >
Aalborg University
Jelsig, A M, Jespersen, N, Karstensen, J G, Ketabi, Z, Rønlund, K, Sunde, L E M, Thorlacius-Ussing, O, Wadt, K A W, Qvist, N & Lautrup, C K 2021, ' Nye arvelige polyposesyndromer som differentialdiagnose hos patienten med tarmpolypper ', Ugeskrift for Laeger, bind 183, V02210148 . < https://ugeskriftet-dk.auh.aub.aau.dk/videnskab/nye-arvelige-polyposesyndromer-som-differentialdiagnose-hos-patienten-med-tarmpolypper >
Jelsig, A M, Jespersen, N, Karstensen, J G, Ketabi, Z, Rønlund, K, Sunde, L, Thorlacius-Ussing, O, Wadt, K, Qvist, N & Lautrup, C K 2021, ' Nye arvelige polyposesyndromer som differentialdiagnose hos patienten med tarmpolypper ', Ugeskrift for Laeger, bind 183, nr. 38, :V02210148 . < https://content.ugeskriftet.dk/sites/default/files/scientific_article_files/2022-03/v02210148_web.pdf >
Jelsig, A M, Jespersen, N, Karstensen, J G, Ketabi, Z, Rønlund, K, Sund, L, Thorlacius-Ussing, O, Wadt, K, Qvist, N & Lautrup, C K 2021, ' Nye arvelige polyposesyndromer som differentialdiagnose hos patienten med tarmpolypper ', Ugeskrift for Læger, bind 183, nr. 38 . < https://ugeskriftet.dk/videnskab/nye-arvelige-polyposesyndromer-som-differentialdiagnose-hos-patienten-med-tarmpolypper >
Fund af tarmpolypper ved endoskopiske undersøgelser er hyppige, idet man antager, at 30-50% af befolkningen har en eller flere polypper i tyktarmen efter 50-årsalderen [1]. Som oftest foretages der polypektomi, og patienten kontrolleres efterfølge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::7e3f8421fe60c6218ae01512f9325cf7
https://portal.findresearcher.sdu.dk/da/publications/d28d5229-8b69-4c77-b8c7-41ab23666c00
https://portal.findresearcher.sdu.dk/da/publications/d28d5229-8b69-4c77-b8c7-41ab23666c00
Autor:
Nicolas Waespe, Marc Ansari, Jean-Pierre Bourquin, Maja Beck-Popovic, Fabiën N. Belle, Jochen Rössler, Shelagh Redmond, Ben D. Spycher, Nicolas von der Weid, Jeanette Greiner, Katrin Scheinemann, Claudia E. Kuehni, Christina Schindera, Freimut H. Schilling, Pierluigi Brazzola
Publikováno v:
European journal of cancer, Vol. 145 (2021) pp. 71-80
Waespe, Nicolas; Belle, Fabiën N.; Redmond, Shelagh; Schindera, Christina; Spycher, Ben D.; Rössler, Jochen; Ansari, Marc; Kuehni, Claudia E. (2021). Cancer predisposition syndromes as a risk factor for early second primary neoplasms after childhood cancer-A national cohort study. European journal of cancer, 145, pp. 71-80. Elsevier 10.1016/j.ejca.2020.11.042
Waespe, Nicolas; Belle, Fabiën N.; Redmond, Shelagh; Schindera, Christina; Spycher, Ben D.; Rössler, Jochen; Ansari, Marc; Kuehni, Claudia E. (2021). Cancer predisposition syndromes as a risk factor for early second primary neoplasms after childhood cancer-A national cohort study. European journal of cancer, 145, pp. 71-80. Elsevier 10.1016/j.ejca.2020.11.042
Background: Childhood cancer patients are at increased risk of second primary neoplasms (SPNs). We assessed incidence and risk factors for early SPNs with a focus on cancer predisposition syndromes (CPSs). Patients and methods: This cohort study used
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cacba93b3aead1ce124526b0cc6cbdda
https://doi.org/10.5167/uzh-213020
https://doi.org/10.5167/uzh-213020
Publikováno v:
Familial cancer, 20(4):289291
Familial Cancer
Ripperger, T, Evans, D G, Malkin, D & Kratz, C P 2021, ' Choose and stay on one out of two paths : distinction between clinical versus research genetic testing to identify cancer predisposition syndromes among patients with cancer ', Familial Cancer, vol. 20, no. 4, pp. 289-291 . https://doi.org/10.1007/s10689-021-00228-2
Fam Cancer
Familial Cancer
Ripperger, T, Evans, D G, Malkin, D & Kratz, C P 2021, ' Choose and stay on one out of two paths : distinction between clinical versus research genetic testing to identify cancer predisposition syndromes among patients with cancer ', Familial Cancer, vol. 20, no. 4, pp. 289-291 . https://doi.org/10.1007/s10689-021-00228-2
Fam Cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa2e87a99c2e30b22832da56874c5c38
https://repository.publisso.de/resource/frl:6446069
https://repository.publisso.de/resource/frl:6446069
Autor:
Fátima Carneiro, Francesco Limarzi, Irene Gullo, Alessandro Vanoli, Luca Mastracci, Matteo Fassan, Luca Saragoni, Federica Grillo, Jacopo Ferro, Paola Parente
Publikováno v:
Pathologica
Summary Gastric cancer accounts for about 6% of cancers worldwide, being the fifth most frequently diagnosed malignancy and the third leading cause of cancer related death. Gastric carcinogenesis is a multistep and multifactorial process and is the r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bcc1a544474a402b14b576c33479024
https://hdl.handle.net/10216/145232
https://hdl.handle.net/10216/145232
Publikováno v:
Schierbeck, J, Vestergaard, T & Bygum, A 2019, ' Skin cancer associated genodermatoses : A literature review ', Acta Dermato-Venereologica, vol. 99, no. 4, pp. 360-369 . https://doi.org/10.2340/00015555-3123
Acta Dermato-Venereologica, Vol 99, Iss 4, Pp 360-369 (2019)
Acta Dermato-Venereologica, Vol 99, Iss 4, Pp 360-369 (2019)
Skin cancer has become the most common type of cancer worldwide as a result of environmental exposure and medical treatments. A small group of patients are genetically predisposed to skin cancer and this article is intended as a diagnostic tool when
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7db0a2e37723a1647442e49d668c46d6
https://findresearcher.sdu.dk:8443/ws/files/149348345/Skin_cancer_associated_genodermatoses.pdf
https://findresearcher.sdu.dk:8443/ws/files/149348345/Skin_cancer_associated_genodermatoses.pdf