Rezultati - Lalloo, Fiona

The pathology of familial breast cancer: Clinical and genetic counselling implications of breast cancer pathology od Lalloo, Fiona, Evans, D Gareth R

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Risk-reducing surgery for ovarian cancer: outcomes in 300 surgeries suggest a low peritoneal primary risk od Evans, D Gareth R, Clayton, Richard, Donnai, Paul, Shenton, Andrew, Lalloo, Fiona

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Penetrance estimates for BRCA1 and BRCA2 based on genetic testing in a Clinical Cancer Genetics service setting: Risks of breast/ovarian cancer quoted should reflect the cancer bur... od Evans, D Gareth, Shenton, Andrew, Woodward, Emma, Lalloo, Fiona, Howell, Anthony, Maher, Eamonn R

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Can multiple SNP testing in BRCA2 and BRCA1 female carriers be used to improve risk prediction models in conjunction with clinical assessment? od Prosperi, Mattia CF, Ingham, Sarah L, Howell, Anthony, Lalloo, Fiona, Buchan, Iain E, Evans, Dafydd Gareth

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Muir–Torre syndrome in a haemodialysis patient od Godfrey, Evonne D., Coward, Robert A., Gharpuray-Pandit, Deepa, Lalloo, Fiona, McKirdy, Stuart, Woywodt, Alexander

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A clinical and genetic analysis of multiple primary cancer referrals to genetics services od Whitworth, James, Hoffman, Jon, Chapman, Cyril, Ong, Kai Ren, Lalloo, Fiona, Evans, D Gareth, Maher, Eamonn R

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Surveillance recommendations for DICER1 pathogenic variant carriers: a report from the SIOPE Host Genome Working Group and CanGene-CanVar Clinical Guideline Working Group od Bakhuizen, Jette J., Hanson, Helen, van der Tuin, Karin, Lalloo, Fiona, Tischkowitz, Marc, Wadt, Karin, Jongmans, Marjolijn C. J.

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Parity and breast cancer risk among BRCA1 and BRCA2 mutation carriers od Antoniou, Antonis C, Shenton, Andrew, Maher, Eamonn R, Watson, Emma, Woodward, Emma, Lalloo, Fiona, Easton, Douglas F, Evans, D Gareth

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Association of Mismatch Repair Mutation With Age at Cancer Onset in Lynch Syndrome: Implications for Stratified Surveillance Strategies od Ryan, Neil A. J., Morris, Julie, Green, Kate, Lalloo, Fiona, Woodward, Emma R., Hill, James, Crosbie, Emma J., Evans, D. Gareth

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30 year experience of index case identification and outcomes of cascade testing in high-risk breast and colorectal cancer predisposition genes od Woodward, Emma R., Green, Kate, Burghel, George J., Bulman, Michael, Clancy, Tara, Lalloo, Fiona, Schlecht, Helene, Wallace, Andrew J., Evans, D. Gareth

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Use of Cytology to Diagnose Inherited Breast Cancer od Møller, Pål, Evans, Gareth, Anderson, Elaine, Mæhle, Lovise, Lalloo, Fiona, Heimdal, Ketil R., Steel, C. Michael, The Biomed 2 Demonstration Programme on Inherited Breast Cancer

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Sensitivity of BRCA1/2 testing in high-risk breast/ovarian/male breast cancer families: little contribution of comprehensive RNA/NGS panel testing od Byers, Helen, Wallis, Yvonne, van Veen, Elke M, Lalloo, Fiona, Reay, Kim, Smith, Philip, Wallace, Andrew J, Bowers, Naomi, Newman, William G, Evans, D Gareth

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Germline FFPE inherited cancer panel testing in deceased family members: implications for clinical management of unaffected relatives od Bennett, Sarah, Alexander, Elizabeth, Fraser, Harry, Bowers, Naomi, Wallace, Andrew, Woodward, Emma R., Lalloo, Fiona, Quinn, Anne Marie, Huang, Shuwen, Schlecht, Helene, Evans, D. Gareth

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BRCA1 and BRCA2 pathogenic variant carriers and endometrial cancer risk: A cohort study od Kitson, Sarah J., Bafligil, Cemsel, Ryan, Neil A.J., Lalloo, Fiona, Woodward, Emma R., Clayton, Richard D., Edmondson, Richard J., Bolton, James, Crosbie, Emma J., Evans, D. Gareth

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Identification of patients with pancreatic adenocarcinoma due to inheritable mutation: Challenges of daily clinical practice od Fulton, Alexander JP, Lamarca, Angela, Nuttall, Christina, McCallum, Lynne, Pihlak, Rille, O’Reilly, Derek, Lalloo, Fiona, McNamara, Mairéad G, Hubner, Richard A, Clancy, Tara, Valle, Juan W

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Uptake of bilateral-risk-reducing-mastectomy: Prospective analysis of 7195 women at high-risk of breast cancer od Evans, D.Gareth, Gandhi, Ashu, Wisely, Julie, Clancy, Tara, Woodward, Emma R., Harvey, James, Highton, Lyndsey, Murphy, John, Barr, Lester, Howell, Sacha J., Lalloo, Fiona, Harkness, Elaine F., Howell, Anthony

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Risk of Contralateral Breast Cancer in Women with and without Pathogenic Variants in BRCA1, BRCA2, and TP53 Genes in Women with Very Early-Onset (<36 Years) Breast Cancer od Hyder, Zerin, Harkness, Elaine F., Woodward, Emma R., Bowers, Naomi L., Pereira, Marta, Wallace, Andrew J., Howell, Sacha J., Howell, Anthony, Lalloo, Fiona, Newman, William G., Smith, Miriam J., Evans, D Gareth

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Specialist oncological surgery for removal of the ovaries and fallopian tubes in BRCA1 and BRCA2 pathogenic variant carriers may reduce primary peritoneal cancer risk to very low l... od Crosbie, Emma J., Flaum, Nicola, Harkness, Elaine F., Clayton, Richard D., Holland, Cathrine, Martin‐Hirsch, Pierre, Wood, Nick, Keating, Patrick, Woodward, Emma R., Lalloo, Fiona, Donnai, Paul, Edmondson, Richard J., Evans, D. Gareth

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Efficacy of Early Diagnosis and Treatment in Women with a Family History of Breast Cancer od Møller, Pål, Reis, Marta M., Evans, Gareth, Vasen, Hans, Haites, Neva, Anderson, Elaine, Steel, C. Michael, Apold, Jaran, Lalloo, Fiona, Mæhle, Lovise, Preece, Paul, Gregory, Helen, Heimdal, Ketil, European Familial Breast Cancer Collaborative Group

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Guidelines for the management of hereditary colorectal cancer from the British Society of Gastroenterology (BSG)/Association of Coloproctology of Great Britain and Ireland (ACPGBI)... od Monahan, Kevin J, Bradshaw, Nicola, Dolwani, Sunil, Desouza, Bianca, Dunlop, Malcolm G, East, James E, Ilyas, Mohammad, Kaur, Asha, Lalloo, Fiona, Latchford, Andrew, Rutter, Matthew D, Tomlinson, Ian, Thomas, Huw J W, Hill, James

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