Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Laura Yarram-Smith"'
Autor:
Robert D Morgan, Andrew R Clamp, Bethany M Barnes, Kirsten Timms, Helene Schlecht, Laura Yarram-Smith, Yvonne Wallis, Mikel Valganon-Petrizan, Suzanne MacMahon, Rhian White, Sian Morgan, Sarah McKenna, Emma Hudson, Laura Tookman, Angela George, Ranjit Manchanda, Sudha S Sundar, Shibani Nicum, James D Brenton, Rebecca S Kristeleit, Susana Banerjee, Iain A McNeish, Jonathan A Ledermann, Stephen S Taylor, D Gareth R Evans, Gordon C Jayson
Publikováno v:
Morgan, R D, Clamp, A R, Barnes, B M, Timms, K, Schlecht, H, Yarram-Smith, L, Wallis, Y, Valganon-Petrizan, M, Macmahon, S, White, R, Morgan, S, Mckenna, S, Hudson, E, Tookman, L, George, A, Manchanda, R, Sundar, S S, Nicum, S, Brenton, J D, Kristeleit, R S, Banerjee, S, Mcneish, I A, Ledermann, J A, Taylor, S S, Evans, D G & Jayson, G C 2023, ' Homologous recombination deficiency in newly diagnosed FIGO stage III/IV high-grade epithelial ovarian cancer: a multi-national observational study ', International Journal of Gynecological Cancer . https://doi.org/10.1136/ijgc-2022-004211
ObjectiveOlaparib plus bevacizumab maintenance therapy improves survival outcomes in women with newly diagnosed, advanced, high-grade ovarian cancer with a deficiency in homologous recombination. We report data from the first year of routine homologo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfb793cc9d756983a33fbb917e7372e8
https://doi.org/10.1136/ijgc-2022-004211
https://doi.org/10.1136/ijgc-2022-004211
Autor:
Lucy Loong, Catherine Huntley, Fiona McRonald, Francesco Santaniello, Joanna Pethick, Bethany Torr, Sophie Allen, Oliver Tulloch, Shilpi Goel, Brian Shand, Tameera Rahman, Margreet Luchtenborg, Alice Garrett, Richard Barber, Tina Bedenham, David Bourn, Kirsty Bradshaw, Claire Brooks, Jonathan Bruty, George J Burghel, Samantha Butler, Chris Buxton, Alison Callaway, Jonathan Callaway, James Drummond, Miranda Durkie, Joanne Field, Lucy Jenkins, Terri P McVeigh, Roger Mountford, Rodney Nyanhete, Evgenia Petrides, Rachel Robinson, Tracy Scott, Victoria Stinton, James Tellez, Andrew J Wallace, Laura Yarram-Smith, Kate Sahan, Nina Hallowell, Diana M Eccles, Paul Pharoah, Marc Tischkowitz, Antonis C Antoniou, D Gareth Evans, Fiona Lalloo, Gail Norbury, Eva Morris, John Burn, Steven Hardy, Clare Turnbull
Publikováno v:
Journal of medical genetics.
Peer reviewed: True
OBJECTIVE: To describe national patterns of National Health Service (NHS) analysis of mismatch repair (MMR) genes in England using individual-level data submitted to the National Disease Registration Service (NDRS) by the NHS
OBJECTIVE: To describe national patterns of National Health Service (NHS) analysis of mismatch repair (MMR) genes in England using individual-level data submitted to the National Disease Registration Service (NDRS) by the NHS
Autor:
Laura Yarram-Smith, Agnieszka Bierzynska, Gavin I. Welsh, Maggie Williams, Moin A. Saleem, P. Dean, C. Buxton, G. Woodward, Ethan S Sen, Gemma Dennis
Publikováno v:
Journal of Medical Genetics
Sen, E S, Dean, P, Yarram-Smith, L, Bierzynska, A, Woodward, G, Buxton, C, Dennis, G, Welsh, G I, Williams, M & Saleem, M A 2017, ' Clinical genetic testing using a custom-designed steroid-resistant nephrotic syndrome gene panel : analysis and recommendations ', Journal of Medical Genetics . https://doi.org/10.1136/jmedgenet-2017-104811
Sen, E S, Dean, P, Yarram-Smith, L, Bierzynska, A, Woodward, G, Buxton, C, Dennis, G, Welsh, G I, Williams, M & Saleem, M A 2017, ' Clinical genetic testing using a custom-designed steroid-resistant nephrotic syndrome gene panel : analysis and recommendations ', Journal of Medical Genetics . https://doi.org/10.1136/jmedgenet-2017-104811
BACKGROUND: There are many single-gene causes of steroid-resistant nephrotic syndrome (SRNS) and the list continues to grow rapidly. Prompt comprehensive diagnostic testing is key to realising the clinical benefits of a genetic diagnosis. This report
Autor:
Ayla Tabaksert, Noel Edwards, Gavin I. Welsh, Hannah L Rhodes, Mark Woodward, Margaret M. Williams, Laura Yarram-Smith, John A. Sayer, Richard J M Coward, Sarah L. Smithson, Alice Hartley, David T. Thwaites, Sarah J. Rice, Charles R.V. Tomson
Background and objectives Cystinuria is a rare inherited renal stone disease. Mutations in the amino acid exchanger System b0,+, the two subunits of which are encoded by SLC3A1 and SLC7A9, predominantly underlie this disease. The work analyzed the ep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10d175ea3437ba0f4699dab2bc36cfaa
https://europepmc.org/articles/PMC4491297/
https://europepmc.org/articles/PMC4491297/
Autor:
Gavin I. Welsh, Sarah F. Smithson, John A. Sayer, Noel Edwards, Mark Woodward, Richard Jm Coward, Laura Yarram-Smith, Ayla Tabaksert, Hannah L Rhodes, Charles R.V. Tomson, David T. Thwaites, Sarah J. Rice, Maggie Williams
Publikováno v:
Nephrology Dialysis Transplantation. 30:iii384-iii384