By Emeritus Professor Allan David Spigelman

Conference Abstracts

Seabrook A; Clifton-Bligh R; Kirk J; Smith J; Spigelman A; Benn D; Tucker K, 2020, 'Prevalence of Hereditary Pheochromocytoma and Paraganglioma and Associated Genotypes Within a Pediatric and Adolescent Population: A Review of Patients Presenting to Familial Cancer Services Within NSW, Australia, Between 1993-2018', in PANCREAS, LIPPINCOTT WILLIAMS & WILKINS, Vol. 49, pp. 486 - 486, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000526823600113&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Han J; Spigelman AD, 2019, 'Adherence to guidelines for the referral of patients with colorectal cancer and abnormal tumour tissue testing for assessment of Lynch syndrome', in ANZ Journal of Surgery, Vol. 89, pp. 1281 - 1285, http://dx.doi.org/10.1111/ans.15054

Macrae F; Spigelman A, 2019, 'Can Butyrate prevent colon cancer? The AusFAP study', in Familial Cancer, Springer (part of Springer Nature), New Zealand, Vol. 18, pp. S86 - S87, presented at International society for gastrointestinal hereditary tumours—insight, New Zealand, 20 March 2019 - 23 March 2019, https://link.springer.com/content/pdf/10.1007%2Fs10689-019-00124-w.pdf

Lynagh L; Danos I; McDonald C; Khan Z; Macrae F; Toh J; Spigelman A, 2019, 'Recruitment to the cancer prevention programme - the New South Wales experience', in Familial Cancer, Springer (part of Springer Nature), New Zealand, Vol. 18, pp. S68 - S69, presented at International Society for gastrointestinal hereditary turmours - INSIGHT, New Zealand, 20 March 2019 - 23 March 2019, https://link.springer.com/content/pdf/10.1007%2Fs10689-019-00124-w.pdf

Lynagh L; Danos I; McDonald C; Spigelman A, 2019, 'A pathway to facilitate referral of patients with abnormal tumour mismatch repair immunohistochemistry to cancer genetics', in Familial Cancer, Springer (part of Springer Nature), Vol. 18, pp. S67 - S68, http://dx.doi.org/10.1007/s10689-019-00124-w

Nichols C; Cops EJ; Michael-Lovatt C; James P; Austin R; Canfell K; Dawkins H; Field M; Goodwin A; Harris M; John T; Kirk J; Lindeman G; Macrae F; Mascarenhas L; McGaughran J; McPike E; Meiser B; Monnick M; Morgan J; Petelin L; Poplawski N; Richardson K; Scott C; Spigelman A; Spurdle AB; Susman R; Trainer A; Tucker K; Ward R; Mitchell G; Pachter N, 2018, 'The ICCon familial cancer database', in ASIA-PACIFIC JOURNAL OF CLINICAL ONCOLOGY, WILEY, Vol. 14, pp. 66 - 67, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000449544200047&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1

Scott RJ; Wong-Brown M; McPhillips M; Dooley S; Spigelman A; Gleeson M; Meldrum C, 2015, 'The curious case of a woman with two BRCA1 mutations in trans', in Hereditary Cancer in Clinical Practice, Springer Science and Business Media LLC, Vol. 13, http://dx.doi.org/10.1186/1897-4287-13-s2-a11

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