Zobrazeno 1 - 10
of 208
pro vyhledávání: '"S. V. Hodgson"'
Autor:
Hill, M J
Publikováno v:
European Journal of Cancer Prevention, 1993 Sep 01. 2(5), 419-419.
Externí odkaz:
https://www.jstor.org/stable/45051148
Publikováno v:
International Journal of Clinical Practice. 56:750-754
Male breast cancer (MBC) is a rare disease with an older average age of presentation than in women. Predisposing factors include increased exposure to oestrogen and being a carrier of a BRCA2 mutation. Most MBC is ductal and the majority are oestroge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88d7606d1ec6486a6ec1e9092059bc60
https://doi.org/10.1111/j.1742-1241.2002.tb11371.x
https://doi.org/10.1111/j.1742-1241.2002.tb11371.x
Publikováno v:
British Journal of Surgery. 84:233-237
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e987b8e2686421f883aacf80f2ed786
https://doi.org/10.1046/j.1365-2168.1997.02700.x
https://doi.org/10.1046/j.1365-2168.1997.02700.x
Publikováno v:
Diseases of the Colon & Rectum. 40:168-171
Patients from a hereditary nonpolyposis colorectal cancer (HNPCC) kindred (Lynch Type 1 and Type 2) have an increased risk of developing large-bowel cancer. Tumors occur at a young age and are characteristically right-sided. Colonic mucosal prolifera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9a495b5d486081d724f8108421edea7
https://doi.org/10.1007/bf02054982
https://doi.org/10.1007/bf02054982
Publikováno v:
British Journal of Surgery. 84:233-237
BACKGROUND: Clinical screening is still the first-line approach to identification of families with hereditary non-polyposis colorectal cancer (HNPCC). The need for uniformity of diagnosis of the syndrome, particularly in multicentre studies, led to t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77f67db47f7aa1432fd9b5e4bf1b517d
https://doi.org/10.1002/bjs.1800840228
https://doi.org/10.1002/bjs.1800840228
Publikováno v:
British Journal of Surgery. 82:14-17
Juvenile polyposis is an uncommon condition characterized by the development of multiple juvenile polyps, predominantly in the colon but also in the rest of the gastrointestinal tract. The condition usually presents in childhood; only 15 per cent of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90edd2b5f2a30f345e6b5c58c910b5ec
https://doi.org/10.1002/bjs.1800820106
https://doi.org/10.1002/bjs.1800820106
Autor:
M H, Nieuwenhuis, C M, Kets, M, Murphy-Ryan, C, Colas, P, Möller, F J, Hes, S V, Hodgson, M J W, Olderode-Berends, S, Aretz, K, Heinimann, E B, Gomez Garcia, F, Douglas, A, Spigelman, S, Timshel, N M, Lindor, H F A, Vasen
Publikováno v:
Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland. 14(9)
Patients with germline phosphatase and tensin homologue (PTEN) mutations develop hamartomatous lesions in several organs and are at increased risk of various malignancies. We assessed the lifetime risk of benign and malignant gastrointestinal lesions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b77cee7863e81e33d51cd1e1b3447776
https://pubmed.ncbi.nlm.nih.gov/22672595
https://pubmed.ncbi.nlm.nih.gov/22672595
Publikováno v:
The British Journal of Radiology. 63:72-75
The Coffin–Lowry syndrome is a rare disorder inherited as an X-linked condition, affecting men much more severely than women. The characteristics are mental retardation, skeletal abnormalities with short stature, hypermobile joints, loose skin, tap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7485707922a2d44d645148cba889d21
https://doi.org/10.1259/0007-1285-63-745-72
https://doi.org/10.1259/0007-1285-63-745-72
Publikováno v:
Clinical genetics. 66(5)
Genetic testing for cancer susceptibility (e.g. hereditary non-polyposis colorectal cancer) is available for some families with a history of colon cancer. Our aim was to investigate participants' anticipated emotional and behavioral reactions to gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9fe86ba3d41348e6b1caff706903ef86
https://pubmed.ncbi.nlm.nih.gov/15479189
https://pubmed.ncbi.nlm.nih.gov/15479189
Autor:
L, Lipton, H J, Thomas, R A, Eeles, R S, Houlston, M, Longmuir, R, Davison, S V, Hodgson, V A, Murday, C G, Norbury, C, Taylor, I P, Tomlinson
Publikováno v:
Familial cancer. 1(3-4)
It is not uncommon for cancer geneticists to be referred families with apparently Mendelian co-inheritance of breast and bowel cancer. Such families present a particular problem as regards the intensity of their screening for these diseases and the u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::438a5327f23f3b3922cb1c722f05147d
https://pubmed.ncbi.nlm.nih.gov/14574178
https://pubmed.ncbi.nlm.nih.gov/14574178