Infinitism: rival or common ground in answering the epistemic regress? von Murday, Brendan

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Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial von Burn, John, Prof Sir, Gerdes, Anne-Marie, Prof, Macrae, Finlay, Prof, Mecklin, Jukka-Pekka, Prof, Moeslein, Gabriela, MD, Olschwang, Sylviane, MD, Eccles, Diane, Prof, Evans, D Gareth, Prof, Maher, Eamonn R, Prof, Bertario, Lucio, MD, Bisgaard, Marie-Luise, MD, Dunlop, Malcolm G, Prof, Ho, Judy WC, MD, Hodgson, Shirley V, Prof, Lindblom, Annika, Prof, Lubinski, Jan, Prof, Morrison, Patrick J, Prof, Murday, Victoria, MD, Ramesar, Raj, Prof, Side, Lucy, MD, Scott, Rodney J, Prof, Thomas, Huw JW, Prof, Vasen, Hans F, Prof, Barker, Gail, Crawford, Gillian, Elliott, Faye, Movahedi, Mohammad, PhD, Pylvanainen, Kirsi, Wijnen, Juul T, PhD, Fodde, Riccardo, Prof, Lynch, Henry T, Prof, Mathers, John C, Prof, Bishop, D Timothy, Prof

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Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study von Movahedi, Mohammad, Bishop, D Timothy, Macrae, Finlay, Mecklin, Jukka-Pekka, Moeslein, Gabriela, Olschwang, Sylviane, Eccles, Diana, Evans, D Gareth, Maher, Eamonn R, Bertario, Lucio, Bisgaard, Marie-Luise, Dunlop, Malcolm G, Ho, Judy W C, Hodgson, Shirley V, Lindblom, Annika, Lubinski, Jan, Morrison, Patrick J, Murday, Victoria, Ramesar, Raj S, Side, Lucy, Scott, Rodney J, Thomas, Huw J W, Vasen, Hans F, Burn, John, Mathers, John C

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Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome) von Mansour, Sahar, Ostergaard, Pia, Simpson, Michael A, Connell, Fiona C, Steward, Colin G, Brice, Glen, Woollard, Wesley J, Dafou, Dimitra, Kilo, Tatjana, Smithson, Sarah, Lunt, Peter, Murday, Victoria A, Hodgson, Shirley, Keenan, Russell, Pilz, Daniela T, Martinez-Corral, Ines, Makinen, Taija, Mortimer, Peter S, Jeffery, Steve, Trembath, Richard C

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Can Self-Forming Actions Dispel Worries about Luck? von Murday, Brendan

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Individual differences in social interaction contexts: Examining the role of personality traits in the degree of self-other integration von Campos-Moinier, Kévin, Murday, Vincent, Brunel, Lionel

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Injury Patterns in Highly Specialized Youth Athletes: A Comparison of 2 Pathways to Specialization von Murday, Patrick F, McLoughlin, Daniel E, Wild, Jacob T, Kwon, Soyang, Burgess, Jamie, LaBella, Cynthia R

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Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2 von Jeffery, Steve, Afzal, Ali R, Rajab, Anna, Fenske, Christiane D, Oldridge, Michael, Elanko, Navaratnam, Ternes-Pereira, Eliana, Tüysüz, Beyhan, Murday, Victoria A, Patton, Michael A, Wilkie, Andrew O.M

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Clinical Presentation and Penetrance of Pheochromocytoma/Paraganglioma Syndromes von Benn, Diana E., Gimenez-Roqueplo, Anne-Paule, Reilly, Jennifer R., Bertherat, Jérôme, Burgess, John, Byth, Karen, Croxson, Michael, Dahia, Patricia L. M., Elston, Marianne, Gimm, Oliver, Henley, David, Herman, Philippe, Murday, Victoria, Niccoli-Sire, Patricia, Pasieka, Janice L., Rohmer, Vincent, Tucker, Kathy, Jeunemaitre, Xavier, Marsh, Deborah J., Plouin, Pierre-François, Robinson, Bruce G.

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Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24 von Brice, G, Mansour, S, Bell, R, Collin, J R O, Child, A H, Brady, A F, Sarfarazi, M, Burnand, K G, Jeffery, S, Mortimer, P, Murday, V A

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Translational nanomedicine: status assessment and opportunities von Murday, James S., PhD, Siegel, Richard W., PhD, Stein, Judith, PhD, Wright, J. Fraser, PhD

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Interleukin‐18 activates Vγ9Vδ2+ T cells from HIV‐positive individuals: recovering the response to phosphoantigen von Murday, Alanna S., Chaudhry, Suchita, Pauza, C. David

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N-terminal pro-brain natriuretic peptide. A new gold standard in predicting mortality in patients with advanced heart failure von Gardner, R S, Ozalp, F, Murday, A J, Robb, S D, McDonagh, T A

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Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome von Laugel, V, Dalloz, C, Durand, M, Sauvanaud, F, Kristensen, U, Vincent, M.C, Pasquier, L, Odent, S, Cormier-Daire, V, Gener, B, Tobias, E.S, Tolmie, J.L, Martin-Coignard, D, Drouin-Garraud, V, Heron, D, Journel, H, Raffo, E, Vigneron, J, Lyonnet, S, Murday, V, Gubser-Mercati, D, Funalot, B, Brueton, L, Sanchez del Pozo, J, Muñoz, E, Gennery, A.R, Salih, M, Noruzinia, M, Prescott, K, Ramos, L, Stark, Z, Fieggen, K, Chabrol, B, Sarda, P, Edery, P, Bloch-Zupan, A, Fawcett, H, Pham, D, Egly, J.M, Lehmann, A.R, Sarasin, A, Dollfus, H

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Virtual reality and its use in post-operative pain following laparoscopy: a feasibility study von Payne, Olivia, Smith, Vinayak, Rolnik, Daniel L., Davies-Tuck, Miranda, Warty, Ritesh, Seo, Densearn, Wetherell, Lima, Murday, Hamsaveni Kalina, Nair, Amrish, Kaur, Rashvinder, Vollenhoven, Beverley

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Long-term effect of resistant starch on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial von Mathers, John C, Prof, Movahedi, Mohammad, PhD, Macrae, Finlay, Prof, Mecklin, Jukka-Pekka, MD, Moeslein, Gabriela, MD, Olschwang, Sylviane, MD, Eccles, Diana, Prof, Evans, Gareth, Prof, Maher, Eamonn R, Prof, Bertario, Lucio, MD, Bisgaard, Marie-Luise, MD, Dunlop, Malcolm, Prof, Ho, Judy WC, MD, Hodgson, Shirley, Prof, Lindblom, Annika, MD, Lubinski, Jan, Prof, Morrison, Patrick J, Prof, Murday, Victoria, MD, Ramesar, Raj, Prof, Side, Lucy, MD, Scott, Rodney J, PhD, Thomas, Huw JW, PhD, Vasen, Hans, MD, Gerdes, Anne-Marie, Prof, Barker, Gail, Crawford, Gillian, MSc, Elliott, Faye, MSc, Pylvanainen, Kirsi, CRA, Wijnen, Juul, PhD, Fodde, Riccardo, Prof, Lynch, Henry, Prof, Bishop, D Timothy, PhD, Burn, John, Prof Sir

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P-D10 IL-18 Reconstitutes Vg9Vd2 T Cells in HIV+ Patient Samples von Murday, Alanna, Pauza, C. David

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Long-term follow-up for keystone design perforator island flap for closure of myelomeningocele von Donaldson, Christopher, Murday, Hamsaveni K. M., Gutman, Matthew J., Maher, Rory, Goldschlager, Tony, Xenos, Chris, Danks, R. Andrew

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Evidence for 28 genetic disorders discovered by combining healthcare and research data von Kaplanis, Joanna, Samocha, Kaitlin E., Wiel, Laurens, Zhang, Zhancheng, Arvai, Kevin J., Eberhardt, Ruth Y., Gallone, Giuseppe, Lelieveld, Stefan H., Martin, Hilary C., McRae, Jeremy F., Short, Patrick J., Torene, Rebecca I., de Boer, Elke, Danecek, Petr, Gardner, Eugene J., Huang, Ni, Lord, Jenny, Martincorena, Iñigo, Pfundt, Rolph, Reijnders, Margot R. F., Yeung, Alison, Yntema, Helger G., Vissers, Lisenka E. L. M., Juusola, Jane, Wright, Caroline F., Brunner, Han G., Firth, Helen V., FitzPatrick, David R., Barrett, Jeffrey C., Hurles, Matthew E., Gilissen, Christian, Retterer, Kyle

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Cost of Hospitalizations During The First Five Years After The Onset Of Spinal Cord Injury: A Population-Based Study Using Billing Records von Cao, Yue, Murday, David, Corley, Elizabeth, DiPiro, Nicole, Krause, James

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