Zobrazeno 1 - 10
of 61
pro vyhledávání: '"hereditary renal cell carcinoma"'
Publikováno v:
Journal of Kidney Cancer and VHL, Vol 10, Iss 4 (2023)
The incidence of renal cell cancer (RCC) is low in individuals aged less than 40 years; however several studies have shown this increasing trend over the years. Hereditary syndromes are associated with RCC and are more frequently observed in early-on
Externí odkaz:
https://doaj.org/article/5434fce455d8487a8475f5cf9490707b
Autor:
Tomás Carminatti, Patricio Aitor García Marchiñena, Ignacio Pablo Tobia González, Valeria de Miguel, Marcelo Martín Serra, Pablo Germán Kalfayan, Alberto Manuel Jurado
Publikováno v:
Journal of Kidney Cancer and VHL, Vol 10, Iss 3 (2023)
Although age younger than 46 years has been an independent criterion for genetic testing in hereditary renal cell carcinoma (hRCC), there is a lack of evidence in the literature. This study aims to analyze whether a 46-year-old cut-off should be cons
Externí odkaz:
https://doaj.org/article/e6283c6b422f414494820c0cea03b344
Publikováno v:
TumorDiagnostik & Therapie. 44:66-72
Zusammenfassung Hintergrund In den letzten Jahren konnten große Fortschritte in der Diagnose und Differenzierung verschiedenster hereditärer Syndrome mit Prädisposition für Nierentumore erzielt werden.Aktuelle Lehrmeinung ist, dass 5–8% aller N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c1313a2a902a847fc68587ee126597d
https://doi.org/10.1055/a-1988-8945
https://doi.org/10.1055/a-1988-8945
Autor:
Christopher J. Ricketts, Berton Zbar, Laura S. Schmidt, W. Marston Linehan, Cathy D. Vocke, Mark W. Ball, Lindsay A. Middelton
Publikováno v:
Human Mutation
Von Hippel‐Lindau (VHL) is a hereditary multisystem disorder caused by germline alterations in the VHL gene. VHL patients are at risk for benign as well as malignant lesions in multiple organs including kidney, adrenal, pancreas, the central nervou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::564cbdef77174b597f4b1ac35500bea8
http://europepmc.org/articles/PMC8068631
http://europepmc.org/articles/PMC8068631
Akademický článek
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Autor:
Gail E. Graham, D.Y.C. Heng, Jean-Baptiste Lattouf, Alan So, Neil Reaume, Michael A.S. Jewett, Simon Tanguay, Lori Wood, Igal Kushnir, Rodney H. Breau, Naveen S. Basappa, Raymond H. Kim, Philippe D. Violette, L. Kirk, Stephen E. Pautler, Melanie Care, Anil Kapoor, Ranjeeta Mallick, Frédéric Pouliot
Publikováno v:
Clinical Oncology. 32:e10-e15
Aims To evaluate the clinical impact of the Canadian criteria for identifying patients and families at risk for hereditary renal cell carcinoma (RCC). Materials and methods The Canadian hereditary RCC risk criteria were applied to patients from 16 ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cdfcf54478a742623898b1777913053
https://doi.org/10.1016/j.clon.2019.07.010
https://doi.org/10.1016/j.clon.2019.07.010
Akademický článek
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Akademický článek
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Autor:
Kayla Fourzali, Dipen J. Parekh, Talia Donenberg, Nicolette C. Vassallo, Priyen M. Patel, Susan H. Blanton, Irman Forghani, Jessica D. Leuchter, Rachel Silva-Smith
Publikováno v:
American journal of medical genetics. Part AREFERENCES. 185(10)
Identifying hereditary syndromes among patients with renal cell carcinoma (RCC) is essential for surveillance of affected individuals and their at-risk family members and for treatment optimization. We conducted a chart review to determine the percen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70ee93092a529ce5a674b6b3ab9afe74
https://pubmed.ncbi.nlm.nih.gov/34152076
https://pubmed.ncbi.nlm.nih.gov/34152076
Autor:
Maher, Eamonn R
Publikováno v:
World Journal of Urology
PURPOSE: Genetic factors have been implicated in the pathogenesis of renal cell carcinoma (RCC), with around 3% of cases having a family history. A greater knowledge of the genetics of inherited RCC has the potential to translate into novel therapeut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b417565ce860ccd95ce1f5610828606e
http://europepmc.org/articles/PMC6280834
http://europepmc.org/articles/PMC6280834