Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ngaire Knight"'
Autor:
Ron Buttenshaw, Gregory J. Anderson, Ngaire Knight, Lisa A. Simms, Barbara A. Leggett, Andrew Bell, Jabbar Tarish, Joanne P. Young
Publikováno v:
Human Mutation. 11:450-455
A family is presented with attenuated familial adenomatous polyposis of variable phenotype. The clinical features range from sparse right-sided polyposis and cancer in the proximal colon at the age of 34 to pan-colonic polyposis and cancer at the age
Autor:
Vicki L. J. Whitehall, Daniel L. Worthley, Ngaire Knight, R Griff Walker, Penny Webb, Barbara A. Leggett, J. K. Landmann, David G. Hewett, David C. Whiteman, Ron Buttenshaw
Publikováno v:
The American journal of gastroenterology. 105(7)
Hyperplastic polyposis syndrome (HPS) confers an increased risk of colorectal cancer and is difficult to manage clinically. Because both polyps and resultant cancers display the CpG island methylator phenotype and mutation of the BRAF oncogene, and b
Autor:
Barbara A. Leggett, Thomas Robertson, Jeanine Young, Jeremy R. Jass, R. L. Buttenshaw, Steven Nasioulas, A Tannenberg, Ngaire Knight, Melissa A. Barker
Publikováno v:
Journal of clinical pathology. 55(3)
Familial adenomatous polyposis (FAP) is an autosomal dominant disorder caused by mutation of the APC gene. It is characterised by the appearance of hundreds to thousands of colorectal adenomas in adolescence and the subsequent development of colorect
Autor:
R. L. Buttenshaw, Ngaire Knight, Barbara A. Leggett, Kelli G. Biden, Joanne P. Young, A E Cowen
Background—Familial adenomatous polyposis usually results in colonic polyposis with hundreds to thousands of polyps, congenital hypertrophy of the retinal pigment epithelium (CHRPE), and variable extracolonic features. Recent reports indicate that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efbd4a0fe0471d0256ad6f212dd7904b
https://europepmc.org/articles/PMC1891546/
https://europepmc.org/articles/PMC1891546/
Publikováno v:
Journal of the American Academy of Dermatology. 31(6)
Background: It is often difficult to differentiate early melanoma from benign pigmented lesions of similar clinical appearance. Objective: Our purpose was to develop a computer image analysis system that has the potential for use as an adjunct to the
Autor:
Georgia Chenevix-Trench, Sue Healey, Ngaire Knight, Barbara A. Leggett, Lesley R. Thomas, Jeffrey Searle
Publikováno v:
Gastroenterology. 105(5)
Background: In familial juvenile polyposis, multiple juvenile polyps occur throughout the colon. The genetic defect has not been characterized. The risk of colon cancer is increased, although the magnitude of the increased risk is controversial. The
Autor:
Thomas Bw, Adèle C. Green, Nicholas G. Martin, Michael G. E. O'Rourke, J Pfitzner, Quintarelli F, McKenzie G, Ngaire Knight
Publikováno v:
Melanoma research. 1(4)
To assist in the distinction of melanoma from benign pigmented lesions, an imaging system was developed, comprising a frame grabber, a microcomputer, a colour video camera and flash lighting with red, green and infrared filters. Over an 18-month peri
Publikováno v:
Melanoma Research. 3:8