Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Vasanti Limbani"'
Autor:
Michael Kennedy, David A. Robinson, Sanjeev Madan, Alison Lewis, Eleanor Keeling, Elke Gemperle-Mannion, Marc J. Philippon, Jamila Kassam, Gavin Bartlett, Joanna Smith, Tahir Mehmood Khan, Mark Norton, Angelos Politis, Wael Dandachli, Venu Kavathapu, Lisa Brackenridge, Steven Borrill, Thomas Bergmann, Andrew MacCauley, Katie Monnington, Rebecca Rowland-Axe, Nicholas R. Parsons, Gayle Githens-Mazer, Tim N. Board, Vasanti Limbani, John O'Donnell, Charles E. Hutchinson, Emma L. Jones, Joanna Stanton, Fraser Pressdee, Thelma Commey, Marcus J K Bankes, Daniel B. Wright, Seb Sturridge, Jas Curtis, Anthony Lewis, Rebecca Fleck, Tracey Taylor, Alison Smeatham, Rebecca McKeown, Miles Callum, Helen Aughwan, Nigel Kiely, Lucie Gosling, Jaclyn Brown, David Cooke, Justine Amero, Felix A. Achana, Philippa Dolphin, Fiona Hammonds, Aresh Hashemi-Nejad, Ajay Malviya, Stephanie Atkinson, Darren Fern, Manoj Ramachandran, Rachel Hobson, Rachel Bray, Damian R. Griffin, Charlotte Nicholls, Marcus Jepson, Alanna Milne, Edward J. Dickenson, Sylvia Turner, Noel Harding, Joanna Whitworth, Dani Moore, Emma Stewart, Kim L Bennell, Charlotte Bryant, Claire Cleary, Karen Boulton, Helen Murray, Stavros Petrou, Faye Moore, Phillip Thomas, Paul Latimer, Jenny L Donovan, Christine Dobb, C. W. McBryde, Michael Cronin, Asim Rajpura, Veronica Cornes, Anna Fouracres, Maria Dubia, Gareth Dickinson, Matthew Wilson, Mark A. Williams, Sam Dawson, David J. Hunter, Martin Beck, Heather Maclintock, Rina Venter, Peter Wall, Katte MacFarlane, Julliet Ball, Peter Morrison, Kirsten Harris, Christopher Edward Bache, Siobhan Stevens, Kelly Bainbridge, Rachel Simmons, Max Fehily, Lynne Graves, Kathryn Poll, Joanna Benfield, Marc George, Craig White, Aslam Mohammed, Abdulkerim Gokturk, Evonne Smith, Jill Goss, Sanjeev Patil, Stephen Eastaugh-Waring, Louise Clarkson, Jo Armstrong, Jim E. Griffin, Giles H. Stafford, Simon Baker, Richard E. Field, John Paul Whitaker, Margaret Pilkington, J. D. Witt, Nadine E. Foster, Matthew Willis, Anna Grice, Alba Realpe, Megan Pinches, Ivor Hughes
Publikováno v:
Griffin, D R, Dickenson, E J, Wall, P D H, Achana, F, Donovan, J L, Griffin, J, Hobson, R, Hutchinson, C E, Jepson, M, Parsons, N R, Petrou, S, Realpe, A, Smith, J, Foster, N E 2018, ' Hip arthroscopy versus best conservative care for the treatment of femoroacetabular impingement syndrome (UK FASHIoN) : a multicentre randomised controlled trial ', Lancet, vol. 391, no. 10136, pp. 2225-2235 . https://doi.org/10.1016/S0140-6736(18)31202-9
Background\ud Femoroacetabular impingement syndrome is an important cause of hip pain in young adults. It can be treated by arthroscopic hip surgery, including reshaping the hip, or with physiotherapist-led conservative care. We aimed to compare the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe660fe24275cf2704ded31a05a38520
https://ora.ox.ac.uk/objects/uuid:65e42016-7e28-4264-9522-4a2e8d2fd518
https://ora.ox.ac.uk/objects/uuid:65e42016-7e28-4264-9522-4a2e8d2fd518
Autor:
Konstantinos, Hatzikotoulas, Andreas, Roposch, Karan M, Shah, Matthew J, Clark, Selina, Bratherton, Vasanti, Limbani, Julia, Steinberg, Eleni, Zengini, Kaltuun, Warsame, Madhushika, Ratnayake, Maria, Tselepi, Jeremy, Schwartzentruber, John, Loughlin, Deborah M, Eastwood, Eleftheria, Zeggini, Manoj, Ramachandran
Publikováno v:
Communications biology. 1
Developmental dysplasia of the hip (DDH) is the most common skeletal developmental disease. However, its genetic architecture is poorly understood. We conduct the largest DDH genome-wide association study to date and replicate our findings in indepen
Autor:
Selina Bratherton, Jeremy Mark Wilkinson, Eleftheria Zeggini, Julia Steinberg, Eleni Zengini, M. Tselepi, Andreas Roposch, Madhushika Ratnayake, M.J. Clark, Vasanti Limbani, Kaltuun Warsame, Konstantinos Hatzikotoulas, Jeremy Schwartzentruber, Karan M. Shah, John Loughlin, Deborah M. Eastwood, Wilkinson Jm
Background: Developmental dysplasia of the hip (DDH) is a common, heritable condition characterised by abnormal formation of the hip joint, but has a poorly understood genetic architecture due to small sample sizes. We apply a novel case-ascertainmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfc7efd86c806148d7df52f44e648bb1
Publikováno v:
Cytotherapy. :1-11