Diagnosis and Management of Hereditary Basal Cell Skin Cancer

Authors: Shanley, Susan, McCormack, Christopher

Source: Recent results in cancer research. 205:191-212

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN606195331&indx=1&recIds=ETOCRN606195331

Current mismatch repair deficiency tumor testing practices and capabilities: A survey of Australian pathology providers.

Authors: Mascarenhas, Lyon¹ Lyon.Mascarenhas@petermac.org, Shanley, Susan¹, Mitchell, Gillian^1,2, Spurdle, Amanda B.³, Macrae, Finlay^4,5, Pachter, Nicholas^6,7, Buchanan, Daniel D.^8,9,10, Ward, Robyn L.¹¹, Fox, Stephen^1,2, Duxbury, Elaine¹², Driessen, Rebecca¹, Boussioutas, Alex^1,2,5

Source: Asia Pacific Journal of Clinical Oncology. Dec2018, Vol. 14 Issue 6, p417-425. 9p.

Subject Terms: *HEREDITARY nonpolyposis colorectal cancer, *COLON cancer, *CANCER cells, *CANCER chemotherapy, *BRAF genes

Basal cell carcinoma tumor suppressor protein

Screening for ovarian cancer in women with varying levels of risk, using annual tests, results in high recall for repeat screening tests

Authors: Nobbenhuis Marielle AE, Bancroft Elizabeth, Moskovic Eleanor, Lennard Fiona, Pharoah Paul, Jacobs Ian, Ward Ann, Barton Desmond PJ, Ind Thomas EJ, Shepherd John H, Bridges Jane E, Gore Martin, Haracopos Chris, Shanley Susan, Ardern-Jones Audrey, Thomas Sarah, Eeles Ros

Source: Hereditary Cancer in Clinical Practice, Vol 9, Iss 1, p 11 (2011)

Subject Terms: ovarian cancer, screening, transvaginal ultrasound, serum CA125, BRCA gene mutation, bilateral salpingo-oophorectomy, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282, Genetics, QH426-470

File Description: electronic resource

Relation: http://www.hccpjournal.com/content/9/1/11; https://doaj.org/toc/1897-4287

Access URL: https://doaj.org/article/53cb5e98dba94f9c9212dccc7356887a

Unusual presentation of Lynch Syndrome

Authors: Yu Veronica PCC, Novelli Marco, Payne Stewart J, Fisher Sam, Barnetson Rebecca A, Frayling Ian M, Barrett Ann, Goudie David, Ardern-Jones Audrey, Eeles Ros, Shanley Susan

Source: Hereditary Cancer in Clinical Practice, Vol 7, Iss 1, p 12 (2009)

Subject Terms: Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282, Genetics, QH426-470

File Description: electronic resource

Relation: http://www.hccpjournal.com/content/7/1/12; https://doaj.org/toc/1897-4287

Access URL: https://doaj.org/article/b4d9e5327d28406fbd99fa39a604a2c8

Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident.

Authors: Wicking, Carol, Shanley, Susan, Smyth, Ian

Source: American Journal of Human Genetics; January 1997, Vol. 60, p21-26, 6p

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Psychosocial effects of whole-body MRI screening in adult high-risk pathogenic TP53mutation carriers: a case-controlled study (SIGNIFY)

Authors: Bancroft, Elizabeth K, Saya, Sibel, Brown, Emma, Thomas, Sarah, Taylor, Natalie, Rothwell, Jeanette, Pope, Jennifer, Chamberlain, Anthony, Page, Elizabeth, Benafif, Sarah, Hanson, Helen, Dias, Alexander, Mikropoulos, Christos, Izatt, Louise, Side, Lucy, Walker, Lisa, Donaldson, Alan, Cook, Jackie A, Barwell, Julian, Wiles, Vicki, Limb, Lauren, Eccles, Diana M, Leach, Martin O, Shanley, Susan, Gilbert, Fiona J, Gallagher, David, Rajashanker, Balashanmugam, Whitehouse, Richard W, Koh, Dow-Mu, Sohaib, S Aslam, Evans, D Gareth, Eeles, Rosalind A, Walker, Leslie G

Source: Journal of Medical Genetics (JMG); 2020, Vol. 57 Issue: 4 p226-236, 11p

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