Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Philip T. Smith"'
Autor:
C. Philip Beaman, Philip T. Smith, Caren A. Frosch, Rachel McCloy, Julian N. Marewski, Rüdiger F. Pohl, Oliver Vitouch
Publikováno v:
Judgment and Decision Making, Vol 5, Pp 258-271 (2010)
Inferences consistent with “recognition-based” decision-making may be drawn for various reasons other than recognition alone. We demonstrate that, for 2-alternative forced-choice decision tasks, less-is-more effects (reduced performance with addi
Externí odkaz:
https://doaj.org/article/462f5acc235846b7ba133331dd3d317e
Autor:
Katherine V. Sadler, Charlie F. Rowlands, Philip T. Smith, Claire L. Hartley, Naomi L. Bowers, Nicola Y. Roberts, Jade L. Harris, Andrew J. Wallace, D. Gareth Evans, Ludwine M. Messiaen, Miriam J. Smith
Publikováno v:
Human Mutation. 43:643-654
Missense variants in the NF2 gene result in variable NF2 disease presentation. Clinical classification of missense variants often represents a challenge, due to lack of evidence for pathogenicity and function. This study provides a summary of NF2 mis
Autor:
Cristina Perez‐Becerril, Andrew J. Wallace, Helene Schlecht, Naomi L. Bowers, Philip T. Smith, Carolyn Gokhale, Helen Eaton, Chris Charlton, Rachel Robinson, Ruth S. Charlton, D. Gareth Evans, Miriam J. Smith
Publikováno v:
Human mutation. 43(10)
Schwannomatosis comprises a group of hereditary tumor predisposition syndromes characterized by, usually benign, multiple nerve sheath tumors, which frequently cause severe pain that does not typically respond to drug treatments. The most common schw
Autor:
Omar N. Pathmanaban, Miriam J. Smith, Simon R. Freeman, Raji Anup, Mary Perry, D. Gareth Evans, Elaine F. Harkness, Emma Stapleton, Roger Laitt, Simon Tobi, Allyson Parry, Rupert Obholzer, Andrew T. King, Naomi L. Bowers, Philip T Smith, Shazia K. Afridi, Mark Kellett, Owen M. Thomas, Chris Duff, Grace Vassallo, Juliette Gair, Andrew J Wallace, Simon K W Lloyd, Scott A. Rutherford, Claire Hartley, Charlotte Hammerbeck-Ward, Stavros Stivaros, Patrick R. Axon, Dorothy Halliday
Publikováno v:
English Specialist NF research group 2019, ' Incidence of mosaicism in 1055 de novo NF2 cases: Much higher than previous estimates with high utility of Next Generation Sequencing. ', Genetics in Medicine . https://doi.org/10.1038/s41436-019-0598-7
PURPOSE: To evaluate the incidence of mosaicism in de novo neurofibromatosis 2 (NF2).METHODS: Patients fulfilling NF2 criteria, but with no known affected family member from a previous generation (n = 1055), were tested for NF2 variants in lymphocyte
Autor:
Susan M. Kemp-Wheeler, Philip T. Smith
Publikováno v:
Unsolved Mysteries of the Mind ISBN: 9781315784960
Unsolved Mysteries of the Mind
Unsolved Mysteries of the Mind
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5e6a50211c2286ef54aaad15b9ea0ae
https://doi.org/10.4324/9781315784960-6
https://doi.org/10.4324/9781315784960-6
Autor:
Adam Shaw, Simon R. Freeman, Miriam J. Smith, Amy E Taylor, Andrew T. King, Philip T Smith, Omar N. Pathmanaban, Simon Tobi, Claire Hartley, Naomi L. Bowers, D. Gareth Evans, Dorothy Halliday, Andrew J Wallace, Simon K W Lloyd, Emma Stapleton, Scott A. Rutherford, Katherine V Sadler, Charlotte Hammerbeck-Ward
Publikováno v:
Journal of medical genetics. 58(4)
ObjectivesCases of sporadic vestibular schwannoma (sVS) have a low rate of association with germline pathogenic variants. However, some individuals with sVS can represent undetected cases of neurofibromatosis type 2 (NF2) or schwannomatosis. Earlier
Autor:
D Gareth, Evans, Claire L, Hartley, Philip T, Smith, Andrew T, King, Naomi L, Bowers, Simon, Tobi, Andrew J, Wallace, Mary, Perry, Raji, Anup, Simon K W, Lloyd, Scott A, Rutherford, Charlotte, Hammerbeck-Ward, Omar N, Pathmanaban, Emma, Stapleton, Simon R, Freeman, Mark, Kellett, Dorothy, Halliday, Allyson, Parry, Juliette J, Gair, Patrick, Axon, Roger, Laitt, Owen, Thomas, Shazia K, Afridi, Rupert, Obholzer, Chris, Duff, Stavros M, Stivaros, Grace, Vassallo, Elaine F, Harkness, Miriam J, Smith
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 22(1)
To evaluate the incidence of mosaicism in de novo neurofibromatosis 2 (NF2).Patients fulfilling NF2 criteria, but with no known affected family member from a previous generation (n = 1055), were tested for NF2 variants in lymphocyte DNA and where ava
Publikováno v:
Mind & Language. 28:661-698
Motivated by accounts of concept use in autistic spectrum disorder (ASD), and a computational model of weak central coherence (O’Loughlin & Thagard, 2000) we examined comprehension and production vocabulary in typically-developing children, and tho
Autor:
Hillary B. Katz, Joseph Leach, Gemma Reynolds, Sue Wilkinson, Philip T. Smith, Victoria Clarke, Alice Jones, Oliver Robinson, Rory Allen, Dorothy Coombs, Annelies Vredeveldt
Publikováno v:
Psychology Learning & Teaching. 9:52-63
Autor:
Philip T. Smith
Publikováno v:
British Journal of Mathematical and Statistical Psychology. 62:195-199
Ranald Roderick Macdonald (1945-2007) was an important contributor to mathematical psychology in the UK, as a referee and action editor for British Journal of Mathematical and Statistical Psychology and as a participant and organizer at the British P