Zobrazeno 1 - 10
of 241
pro vyhledávání: '"Giardiello, F"'
Autor:
Trimbath, J. D.1 (AUTHOR), Giardiello, F. M.1,2 (AUTHOR)
Publikováno v:
Alimentary Pharmacology & Therapeutics. Nov2002, Vol. 16 Issue 11, p1843-1857. 15p. 6 Charts.
Autor:
de Leng, W W J, Jansen, M, Keller, J J, de Gijsel, M, Milne, A N A, Morsink, F H M, Weterman, M A J, Iacobuzio‐Donahue, C A, Clevers, H C, Giardiello, F M, Offerhaus, G J A
Publikováno v:
Gut, 56(10), 1475-1476. BMJ Publishing Group
Peutz–Jeghers syndrome (PJS) is an autosomal dominant cancer susceptibility syndrome characterised by mucocutaneous melanin pigmentation, hamartomatous polyps, and an 18-fold increase in intestinal and extraintestinal cancer risk.1 PJS is caused by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::011b6144475dbdb25eff76d6c56116ec
https://europepmc.org/articles/PMC2000288/
https://europepmc.org/articles/PMC2000288/
Autor:
Keller, J. J., Offerhaus, G. J., Drillenburg, P., Caspers, E., Musler, A., Ristimäki, A., Giardiello, F. M.
Publikováno v:
Clinical cancer research, 7(12), 4000-4007. American Association for Cancer Research Inc.
Sulindac causes the reduction of adenomas in familial adenomatous polyposis (FAP) patients, but complete regression is unusual, and breakthrough of colorectal carcinoma during sulindac treatment has been described. The molecular features related to s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::6c7b2d61f811d128b4861921ce74dce4
https://pure.amc.nl/en/publications/molecular-analysis-of-sulindacresistant-adenomas-in-familial-adenomatous-polyposis(f74fdf98-8b4e-4bfe-99e4-1f133432d367).html
https://pure.amc.nl/en/publications/molecular-analysis-of-sulindacresistant-adenomas-in-familial-adenomatous-polyposis(f74fdf98-8b4e-4bfe-99e4-1f133432d367).html
Publikováno v:
Familial cancer, 1(3-4), 181-185. Springer Netherlands
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::de1f60bf32eed5423ce84b9eb20cdc1f
https://pure.amc.nl/en/publications/jan-peutz-harold-jeghers-and-a-remarkable-combination-of-polyposis-and-pigmentation-of-the-skin-and-mucous-membranes(2a8622d4-4a19-40f2-a189-8011ce42b202).html
https://pure.amc.nl/en/publications/jan-peutz-harold-jeghers-and-a-remarkable-combination-of-polyposis-and-pigmentation-of-the-skin-and-mucous-membranes(2a8622d4-4a19-40f2-a189-8011ce42b202).html
Autor:
Entius, M. M., Keller, J. J., Drillenburg, P., Kuypers, K. C., Giardiello, F. M., Offerhaus, G. J.
Publikováno v:
Clinical cancer research, 6(5), 1784-1789. American Association for Cancer Research Inc.
Sebaceous gland carcinomas (SGCs) are rare malignant skin tumors occurring sporadically or as a phenotypic feature of the Muir-Torre syndrome (MTS). A subset of patients with MTS have a variant of the hereditary nonpolyposis colorectal cancer syndrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::e3e90c01e05acb6464be7effa7b29770
https://pure.amc.nl/en/publications/microsatellite-instability-and-expression-of-hmlh1-and-hmsh2-in-sebaceous-gland-carcinomas-as-markers-for-muirtorre-syndrome(e9fa493a-b92f-49aa-ad31-fff6da6b8aaa).html
https://pure.amc.nl/en/publications/microsatellite-instability-and-expression-of-hmlh1-and-hmsh2-in-sebaceous-gland-carcinomas-as-markers-for-muirtorre-syndrome(e9fa493a-b92f-49aa-ad31-fff6da6b8aaa).html
Publikováno v:
Hepato-gastroenterology, 46(26), 667-669. H.G.E. Update Medical Publishing Ltd.
Familial adenomatous polyposis (FAP) is an autosomal dominant disease in which affected family members develop numerous colorectal adenomas with a virtually 100% chance of malignant degeneration unless the colon is prophylactically removed. After col
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::31ad59d385047c3eaadbd2e58c059c49
https://pure.amc.nl/en/publications/upper-gastrointestinal-polyps-in-familial-adenomatous-polyposis(a0d4a1c5-c6c7-4ca0-916c-5c6fff8557a5).html
https://pure.amc.nl/en/publications/upper-gastrointestinal-polyps-in-familial-adenomatous-polyposis(a0d4a1c5-c6c7-4ca0-916c-5c6fff8557a5).html
Autor:
Entius, M. M., Westerman, A. M., van Velthuysen, M. L., Wilson, J. H., Hamilton, S. R., Giardiello, F. M., Offerhaus, G. J.
Publikováno v:
Hepato-gastroenterology, 46(26), 661-666. H.G.E. Update Medical Publishing Ltd.
Hamartomatous gastrointestinal polyposis syndromes have always been considered as non-neoplastic. Nevertheless, an increased cancer risk both within and outside the gastrointestinal tract may exist in these syndromes. The hamartomatous polyps may som
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::83fc03e1b13beef55c080401340e53a7
https://pure.amc.nl/en/publications/molecular-and-phenotypic-markers-of-hamartomatous-polyposis-syndromes-in-the-gastrointestinal-tract(8747402c-05b4-47b7-86f3-381f053cea45).html
https://pure.amc.nl/en/publications/molecular-and-phenotypic-markers-of-hamartomatous-polyposis-syndromes-in-the-gastrointestinal-tract(8747402c-05b4-47b7-86f3-381f053cea45).html
Autor:
Gruber, S. B., Entius, M. M., Petersen, G. M., Laken, S. J., Longo, P. A., Boyer, R., Levin, A. M., Mujumdar, U. J., Trent, J. M., Kinzler, K. W., Vogelstein, B., Hamilton, S. R., Polymeropoulos, M. H., Offerhaus, G. J., Giardiello, F. M.
Publikováno v:
Cancer research, 58(23), 5267-5270. American Association for Cancer Research Inc.
Peutz-Jeghers syndrome (PJS) is an autosomal dominant condition characterized by intestinal hamartomatous polyps, mucocutaneous melanin deposition, and increased risk of cancer. Families with PJS from the Johns Hopkins Polyposis Registry were studied
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::fef5e4a1f19d2aafc31ab13e14e21c42
https://pure.amc.nl/en/publications/pathogenesis-of-adenocarcinoma-in-peutzjeghers-syndrome(e24daa1f-d612-4866-9c6a-3bda296cf54f).html
https://pure.amc.nl/en/publications/pathogenesis-of-adenocarcinoma-in-peutzjeghers-syndrome(e24daa1f-d612-4866-9c6a-3bda296cf54f).html
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.