Výsledky vyhledávání - Louise Izatt
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p.Val804Met, the Most Frequent Pathogenic Mutation in RET, Confers a Very Low Lifetime Risk of Medullary Thyroid Cancer Autor Chey Loveday, Katherine Josephs, Daniel Chubb, Adam C. Gunning, Louise Izatt, Marc Tischkowitz, Sian Ellard, Clare Turnbull
Vydáno 2018Artigo -
2
UKCGG Consensus Group guidelines for the management of patients with constitutional <i>TP53</i> pathogenic variants Autor Helen Hanson, Angela F. Brady, Gillian Crawford, Rosalind A. Eeles, S. L. Gibson, Mette Jorgensen, Louise Izatt, Aslam Sohaib, Marc Tischkowitz, D. Gareth Evans
Vydáno 2020Artigo -
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Paediatric differentiated thyroid carcinoma: a UK National Clinical Practice Consensus Guideline Autor Sasha Howard, Sarah Freeston, Barney Harrison, Louise Izatt, Sonali Natu, Kate Newbold, Sabine Pomplun, Helen Spoudeas, Sophie Wilne, Tom Kurzawinski, Mark N. Gaze
Vydáno 2022Artigo -
4
The Angelina Jolie effect: how high celebrity profile can have a major impact on provision of cancer related services Autor D. Gareth Evans, Julian Barwell, Diana Eccles, Amanda Collins, Louise Izatt, Chris Jacobs, Alan C. Donaldson, Angela F. Brady, Andrew Cuthbert, Rachel Harrison, Sue Thomas, Anthony Howell, Zosia Miedzybrodzka, Alex Murray
Vydáno 2014Artigo -
5
Society for Endocrinology <scp>UK</scp> guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development (Revised 2015) Autor S. Faisal Ahmed, John C. Achermann, Wiebke Arlt, Adam Balen, Gerry Conway, Zoe Edwards, Sue Elford, Ieuan A. Hughes, Louise Izatt, Nils Krone, Harriet Miles, Stuart O’Toole, Les Perry, Caroline Sanders, Margaret Simmonds, Andrew Watt, Debbie Willis
Vydáno 2015Carta -
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UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development Autor S. Faisal Ahmed, John C. Achermann, Wiebke Arlt, Adam Balen, Gerry Conway, Zoe Edwards, Sue Elford, Ieuan A. Hughes, Louise Izatt, Nils Krone, Harriet Miles, Stuart O’Toole, Les Perry, Caroline Sanders, Margaret Simmonds, Andrew Wallace, Andrew Watt, Debbie Willis
Vydáno 2011Artigo -
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Large Genomic Deletions in<i>AIP</i>in Pituitary Adenoma Predisposition Autor Marianthi Georgitsi, Elina Heliövaara, Ralf Paschke, Ajith Kumar, Marc Tischkowitz, Outi Vierimaa, Pasi Salmela, Timo Sane, Ernesto De Menis, Salvatore Cannavò, Sadi Gündoğdu, Anneke Lucassen, Louise Izatt, Simon Aylwin, Gul Bano, Shirley Hodgson, Christian A. Koch, Auli Karhu, Lauri A. Aaltonen
Vydáno 2008Artigo -
8
2022 European Thyroid Association Guidelines for the management of pediatric thyroid nodules and differentiated thyroid carcinoma Autor Chantal A Lebbink, Thera P. Links, Agnieszka Czarniecka, Renuka Dias, Rossella Elisei, Louise Izatt, Heiko Krude, Kerstin Lorenz, Markus Luster, Kate Newbold, Arnoldo Piccardo, Manuel Sobrinho‐Simões, Toru Takano, A.S. Paul van Trotsenburg, Frederik A. Verburg, Hanneke M. van Santen
Vydáno 2022Artigo -
9
Mammographic Density and Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers Autor Gillian Mitchell, Antonis C. Antoniou, Ruth Warren, Susan Peock, Judith Brown, R.S.M. Davies, Jenny Mattison, Margaret Cook, Iqbal Warsi, D. Gareth Evans, Diana Eccles, Fiona Douglas, Joan Paterson, Shirley Hodgson, Louise Izatt, Trevor Cole, Lucy Burgess, Rosalind A. Eeles, Douglas F. Easton
Vydáno 2006Artigo -
10
Germline PRKACA amplification causes variable phenotypes that may depend on the extent of the genomic defect: molecular mechanisms and clinical presentations Autor Maya Lodish, Bo Yuan, Isaac Lévy, Glenn D. Braunstein, Charalampos Lyssikatos, Calvin Ke, Eva Szarek, Alexander S. Karageorgiadis, Elena Belyavskaya, Margarita Raygada, Fábio R. Faucz, Louise Izatt, Caroline Brain, James L. Gardner, Martha Quezado, J. Aidan Carney, James R. Lupski, Constantine A. Stratakis
Vydáno 2015Artigo -
11
Cancer Precision-Prevention trial of Metformin in adults with Li Fraumeni syndrome (MILI) undergoing yearly MRI surveillance: a randomised controlled trial protocol Autor Miriam Dixon-Zegeye, Rachel Shaw, Linda M. Collins, Kendra Perez-Smith, Alexander Ooms, Maggie Qiao, Pan Pantziarka, Louise Izatt, Marc Tischkowitz, Rachel E. Harrison, Angela George, Emma R. Woodward, Simon Lord, Lara Hawkes, D. Gareth Evans, James Franklin, Helen Hanson, Sarah P. Blagden
Vydáno 2024Artigo -
12
A Comprehensive Next Generation Sequencing–Based Genetic Testing Strategy To Improve Diagnosis of Inherited Pheochromocytoma and Paraganglioma Autor Eleanor Rattenberry, Lindsey Vialard, Anna C. Y. Yeung, Hayley Bair, Kirsten McKay, Mariam Jafri, Natalie Canham, Trevor Cole, Judit Dénes, Shirley V. Hodgson, Richard Irving, Louise Izatt, Márta Korbonits, Ajith Kumar, Fiona Lalloo, Patrick J. Morrison, Emma R. Woodward, Fiona MacDonald, Yvonne Wallis, Eamonn R. Maher
Vydáno 2013Artigo -
13
When Genetic Load Does Not Correlate with Phenotypic Spectrum: Lessons from the GnRH Receptor (<i>GNRHR</i>) Autor Elena Gianetti, Janet E. Hall, Margaret Au, Ursula B. Kaiser, Richard Quinton, Jane A. Stewart, Daniel L. Metzger, Nelly Pitteloud, Verónica Mericq, Paulina M. Merino, Lynne L. Levitsky, Louise Izatt, Mariarosaria Lang‐Muritano, Victor Y. Fujimoto, Robert G. Dluhy, Matthew Chase, William F. Crowley, Lacey Plummer, Stephanie B. Seminara
Vydáno 2012Artigo -
14
Germline CDKN1B/p27Kip1 Mutation in Multiple Endocrine Neoplasia Autor Marianthi Georgitsi, Anniina Raitila, Auli Karhu, Rob B. van der Luijt, Cora M. Aalfs, Timo Sane, Outi Vierimaa, Markus J. Mäkinen, Karoliina Tuppurainen, R Paschke, Oliver Gimm, Christian A. Koch, Sadi Gündoğdu, Anneke Lucassen, Marc Tischkowitz, Louise Izatt, Simon Aylwin, Gul Bano, Shirley Hodgson, Ernesto De Menis, Virpi Launonen, Pia Vahteristo, Lauri A. Aaltonen
Vydáno 2007Artigo -
15
<scp>SDHA</scp> related tumorigenesis: a new case series and literature review for variant interpretation and pathogenicity Autor Ruth Casey, David B. Ascher, Eleanor Rattenberry, Louise Izatt, Katrina Andrews, Helen Simpson, Benjamen G Challis, Soo‐Mi Park, V.R. Bulusu, Fiona Lalloo, Douglas E. V. Pires, Hannah D. West, Graeme R. Clark, Philip Smith, James W. Whitworth, Thomas Papathomas, Phillipe Taniere, Rosina Savisaar, Laurence D. Hurst, Emma R. Woodward, Eamonn R. Maher
Vydáno 2017Artigo -
16
Cancer Variant Interpretation Group UK (CanVIG-UK): an exemplar national subspecialty multidisciplinary network Autor Alice Garrett, Alison Callaway, Miranda Durkie, Cankut Çubuk, Mary Alikian, George J. Burghel, Rachel Robinson, Louise Izatt, Sabrina Talukdar, Lucy Side, Treena Cranston, Sheila Palmer-Smith, Diana Baralle, Ian Berry, James Drummond, Andrew Wallace, Gail Norbury, Diana Eccles, Sian Ellard, Fiona Lalloo, D. Gareth Evans, Emma R. Woodward, Marc Tischkowitz, Helen Hanson, Clare Turnbull
Vydáno 2020Artigo -
17
Quantification of sequence exchange events between<i>PMS2</i>and<i>PMS2CL</i>provides a basis for improved mutation scanning of Lynch syndrome patients Autor Heleen M. van der Klift, Carli M.J. Tops, Elsa C. Bik, Merel W. Boogaard, Anne-Marijke Borgstein, Kerstin Hansson, Margreet G.E.M. Ausems, E. Gómez, Andrew Green, Frederik J. Hes, Louise Izatt, Liselotte P. van Hest, Ángel Alonso, A. H. J. T. Vriends, Anja Wagner, Wendy A.G. van Zelst–Stams, Hans F. A. Vasen, Hans Morreau, Peter Devilee, Juul Wijnen
Vydáno 2010Artigo -
18
Tumor risks and genotypeâphenotypeâproteotype analysis in 358 patients with germline mutations in<i>SDHB</i>and<i>SDHD</i> Autor Christopher J. Ricketts, Julia Forman, Eleanor Rattenberry, Nicola Bradshaw, Fiona Lalloo, Louise Izatt, Trevor Cole, Ruth Armstrong, V K Ajith Kumar, Patrick J. Morrison, A. Brew Atkinson, Fiona Douglas, Steve Ball, Jackie Cook, Umasuthan Srirangalingam, Pip Killick, Gail Kirby, Simon Aylwin, Emma R. Woodward, D. Gareth Evans, Shirley V. Hodgson, V Murday, Shern L. Chew, John Connell, Tom L. Blundell, Fiona MacDonald, Eamonn R. Maher
Vydáno 2009Artigo -
19
Evaluation of <scp>SDHB</scp>,<scp> SDHD</scp> and <scp>VHL</scp> gene susceptibility testing in the assessment of individuals with non‐syndromic phaeochromocytoma, paraganglioma a... Autor Mariam Jafri, James W. Whitworth, Eleanor Rattenberry, Lindsey Vialard, Gail Kilby, Ajith Kumar, Louise Izatt, Fiona Lalloo, Paul Brennan, Jackie Cook, Patrick J. Morrison, Natalie Canham, Ruth Armstrong, Carole Brewer, Susan Tomkins, Alan Donaldson, Julian Barwell, Trevor Cole, A. Brew Atkinson, Simon Aylwin, Steve Ball, Umasuthan Srirangalingam, Shern L. Chew, D. Gareth Evans, Shirley V. Hodgson, Richard Irving, Emma R. Woodward, Fiona MacDonald, Eamonn R. Maher
Vydáno 2012Artigo -
20
Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesis Autor Stephen R.F. Twigg, Elena Vorgia, Simon J. McGowan, Ioanna Peraki, Aimée L Fenwick, Vikram Sharma, Maryline Allégra, Ανδρέας Ζαραγκούλιας, Elham Sadighi Akha, Samantha J.L. Knight, Helen Lord, Tracy Lester, Louise Izatt, Anne Katrin Lampe, Shehla Mohammed, Fiona J. Stewart, Alain Verloès, Louise C. Wilson, Chris Healy, Paul T. Sharpe, Peter Hammond, Jim R. Hughes, Stephen Taylor, David Johnson, Steven A. Wall, George Mavrothalassitis, Andrew O.M. Wilkie
Vydáno 2013Artigo
Vyhledávací nástroje:
Související témata
Medicine
Biology
Genetics
Gene
Internal medicine
Cancer
Mutation
Oncology
Breast cancer
Germline mutation
Genotype
Pathology
Cancer research
Gynecology
Phenotype
Allele
Single-nucleotide polymorphism
Environmental health
Family medicine
Gene expression
Genetic testing
Germline
Ovarian cancer
Population
Prostate cancer
Bioinformatics
Penetrance
Prostate
Surgical oncology
BRCA2 Protein