Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ursula Algar"'
Autor:
Safiye Yildiz, Takudzwa N. Musarurwa, Ursula Algar, Ramadhani Chambuso, George Rebello, Paul A. Goldberg, Raj Ramesar
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
IntroductionThe increase in incidence of colorectal cancer in young patients of African ancestry coupled with increased aggressiveness has warranted investigation of the heritable nature of these cancers. Only a limited number of published reports of
Externí odkaz:
https://doaj.org/article/bb66de43fbfb493f8fc1bc8f1b6c00d2
Autor:
Yasmina Johnson, Paul Goldberg, Jennifer Moodley, Ursula Algar, Sandie Thomson, Edina Sinanovic, Raj Ramesar
Publikováno v:
Cancer causescontrol : CCC.
Lynch Syndrome (LS) individuals have a 25-75% lifetime risk of developing colorectal cancer. Colonoscopy screening decreases this risk. This study compared the cost of Strategy 1: screening colonoscopy for 1st degree relatives of patients that met th
Autor:
Helen Wainwright, Alvera Vorster, Ursula Algar, P. A. Goldberg, Zandrè Bruwer, Alan Davidson, Karen Fieggen, Rajkumar Ramesar
Publikováno v:
Journal of genetic counseling. 23(2)
Biallelic germline mutations in mismatch repair genes predispose to constitutional mismatch repair deficiency syndrome (CMMR-D). The condition is characterized by a broad spectrum of early-onset tumors, including hematological, brain and bowel and is
Autor:
N. Mbatani, G. E. Pietersen, L. van der Merwe, M. M. Blokhuis, P. A. Goldberg, Rajkumar Ramesar, Ursula Algar, A. A. Vorster
Publikováno v:
Groen-Blokhuis, M M, Pietersen, G E, Goldberg, P A, Algar, U, Van der Merwe, L, Mbatani, N, Vorster, A A & Ramesar, R S 2010, ' Lynch syndrome: the influence of environmental factors on extracolonic cancer risk in hMLH1 c.C1528T mutation carriers and their mutation-negative sisters ', Familial Cancer, vol. 9, no. 3, pp. 357-363 . https://doi.org/10.1007/s10689-010-9334-9
Familial Cancer, 9(3), 357-363. Springer Netherlands
Familial Cancer, 9(3), 357-363. Springer Netherlands
Lynch Syndrome (LS) is a cancer susceptibility syndrome caused mostly by mutations in the mismatch repair genes, hMLH1, hMSH2 and hMSH6. Mutation carriers are at risk of colorectal and endometrial cancer and, less frequently, cancer of the ovaries, s
Publikováno v:
Hereditary Colorectal Cancer ISBN: 9781441966025
Hereditary nonpolyposis colorectal cancer (HNPCC), an autosomal dominant condition caused by mutations in the mismatch repair genes, accounts for 20–35% of inherited cancers and 1–7% of colorectal cancers (CRC). Colonoscopic surveillance reduces
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19679a01b5dcb97024d3a35d76ed525a
https://doi.org/10.1007/978-1-4419-6603-2_28
https://doi.org/10.1007/978-1-4419-6603-2_28
The extracolonic cancer spectrum in females with the common ‘South African’ hMLH1 c.C1528T mutation.
Publikováno v:
Familial Cancer; Sep2008, Vol. 7 Issue 3, p191-198, 8p, 4 Charts