Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Theresa Berk"'
Publikováno v:
Diseases of the Colon & Rectum. 42:307-310
PURPOSE: The goal of genetic testing is to define individual risk, which in turn may guide clinical management. METHODS: Thirty-two international familial adenomatous polyposis registries were surveyed regarding their approach to a specific clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82ebd7d5c299c594553e03d5a551e794
https://doi.org/10.1007/bf02236343
https://doi.org/10.1007/bf02236343
Publikováno v:
International Journal of Colorectal Disease. 12:14-18
Background: Gastro-duodenal polyps develop in up to 90% of familial adenomatous polyposis (FAP) patients and periampullary carcinoma is one of the most common extra-colonic malignancies in this syndrome. Periampullary adenomas have been shown to be p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42cd2c4e6a6009da93a583ff327a1e4c
https://doi.org/10.1007/s003840050071
https://doi.org/10.1007/s003840050071
Publikováno v:
Diseases of the Colon & Rectum. 39:384-387
Widespread use of prophylactic colectomy has resulted in a reduction in the incidence of colorectal cancer in familial adenomatous polyposis (FAP) patients. A retrospective chart review of families registered at the Steve Atanas Stavro Familial Gastr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82806afc50b986da917364f697507e62
https://doi.org/10.1007/bf02054051
https://doi.org/10.1007/bf02054051
Autor:
Theresa Berk, Bharati Bapat, Juan Ramon Sanabria, Ruth Croxford, Steven Gallinger, Zane Cohen
Publikováno v:
The American Journal of Surgery. 171:136-141
Familial adenomatous polyposis (FAP) patients often develop periampullary adenomas that may progress to periampullary cancer, a common cause of death in this population. The risk of periampullary cancer in FAP is unclear, and variables that predict t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7a975748792feb1834415f90f9e3853
https://doi.org/10.1016/s0002-9610(99)80088-9
https://doi.org/10.1016/s0002-9610(99)80088-9
Autor:
Francis M. Giardiello, G. Johan A. Offerhaus, Anne C. Tersmette, Steven M. Powell, Ramon Parsons, Zane Cohen, Anne J. Krush, Fowzia Taqi, Kenneth W. Kinzler, Bert Vogelstein, Nickolas Papadopoulos, Gloria M. Petersen, Bernard Têtu, Jin Jen, Patricia A. Wood, Theresa Berk, Susan V. Booker, Bo Liu, Stanley R. Hamilton, Peter C. Burger
Publikováno v:
New England Journal of Medicine. 332:839-847
Turcot's syndrome is characterized clinically by the concurrence of a primary brain tumor and multiple colorectal adenomas. We attempted to define the syndrome at the molecular level.Fourteen families with Turcot's syndrome identified in two registri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4651c91cd14e88a526b70de188c3a985
https://doi.org/10.1056/nejm199503303321302
https://doi.org/10.1056/nejm199503303321302
Publikováno v:
Diseases of the colon and rectum. 55(4)
BACKGROUND The major manifestation of familial adenomatous polyposis is colorectal adenomas, which, if untreated, lead to colorectal cancer. The impact of IPAA on quality of life in adolescents with familial adenomatous polyposis is favorable. There
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86be5ae92eef41f57a427af5ba0650fd
https://pubmed.ncbi.nlm.nih.gov/22426268
https://pubmed.ncbi.nlm.nih.gov/22426268
Autor:
Hartley Stern, John A. Parker, Peter N. Ray, Robin S. McLeod, Bharati Bapat, Theresa Berk, Zane Cohen
Publikováno v:
Diseases of the Colon & Rectum. 37:165-171
Predictive carrier testing for the inherited disorder of familial adenomatous polyposis (FAP) can be conducted using DNA markers linked to the FAP locus. The presence of characteristic hypertrophic retinal lesions has been advocated as useful biomark
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5856f2486fe460cc6ec39718a125986e
https://doi.org/10.1007/bf02047541
https://doi.org/10.1007/bf02047541
Autor:
Theresa Berk, Hartley Stern
Publikováno v:
Gastrointestinal Endoscopy Clinics of North America. 3:725-736
The natural history of familial adenomatous polyposis (FAP) has been greatly improved with the advent of registries whose mandate is to improve the detection and management of affected individuals and their families, and to develop new knowledge conc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e3adc17a9dc27691615f03bb1b46b55
https://doi.org/10.1016/s1052-5157(18)30543-9
https://doi.org/10.1016/s1052-5157(18)30543-9
Publikováno v:
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association. 5(10)
Background & Aims: Desmoid tumors are non-metastasizing fibromatoses that occur in 10%–20% of subjects with familial adenomatous polyposis (FAP). Intra-abdominal desmoid tumors are a major cause of mortality in FAP. FAP-associated desmoid tumors ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1238565ac56b71e2671382af1196e34
https://pubmed.ncbi.nlm.nih.gov/17916546
https://pubmed.ncbi.nlm.nih.gov/17916546
Autor:
A S Detsky, Steve Gallinger, Theresa Berk, K Pritzker, Bharati Bapat, H Z Noorani, Brenda L. Gallie, Angela Mitri, Zane Cohen
Publikováno v:
Gut. 44(5)
BACKGROUNDMutations of theAPC gene cause familial adenomatous polyposis (FAP), a hereditary colorectal cancer predisposition syndrome.AIMSTo conduct a cost comparison analysis of predictive genetic testing versus conventional clinical screening for i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e503a8f652207fa0e490b39b1e5f64eb
https://pubmed.ncbi.nlm.nih.gov/10205208
https://pubmed.ncbi.nlm.nih.gov/10205208