Showing 1 - 20 results of 21 for search 'Williamson K', query time: 0.06s
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Editorial: further evidence for the role of serum alkaline phosphatase as a useful surrogate marker of prognosis in PSC. by Williamson, K, Chapman, R
Published 2015Journal article -
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Are dominant strictures in primary sclerosing cholangitis a risk factor for cholangiocarcinoma? by Chapman, R, Williamson, K
Published 2017Journal article -
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The Rapid Assessment Interface and Discharge service and its implications for patients with dementia by Singh I, Ramakrishna S, Williamson K
Published 2013-08-01
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Lesson of the week: Danger of stereotyping in suspected osteomalacia. by Sheikh, S, Williamson, K, Kearley, K, Bassindale, S, Lancaster, T
Published 2001Journal article -
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Biliary transporter gene mutations in severe intrahepatic cholestasis of pregnancy: Diagnostic and management implications by Yeap, S, Harley, H, Thompson, R, Williamson, K, Bate, J, Sethna, F, Farrell, G, Hague, W
Published 2018Journal article -
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A novel prognostic model for transplant-free survival in primary sclerosing cholangitis by de Vries, E, Wang, J, Williamson, K, Leeflang, M, Boonstra, K, Weersma, R, Beuers, U, Chapman, R, Geskus, R, Ponsioen, C
Published 2017Journal article -
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Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects. by Williamson, K, Rainger, J, Floyd, J, Ansari, M, Meynert, A, Aldridge, K, Rainger, J, Anderson, C, Moore, A, Hurles, M, Clarke, A, van Heyningen, V, Verloes, A, Taylor, MS, Wilkie, A, Fitzpatrick, DR
Published 2014Journal article -
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International experience of vedolizumab in primary sclerosing cholangitis and inflammatory bowel disease by Williamson, K, Lytvyak, E, De Krijger, M, Trivedi, P, Estes, D, Yu, L, Pratt, D, De Vries, A, Daretti, L, Liu, C, Bowlus, C, Marschall, H, Montano-Loza, A, Chapman, R, Van Der Woude, C, Marzioni, M, Keshav, S, Ponsioen, C, Hirschfield, G, Levy, C
Published 2018Conference item -
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Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism by Ansari, M, Poke, G, Ferry, Q, Williamson, K, Aldridge, R, Meynert, A, Bengani, H, Chan, C, Kayserili, H, Avci, Ş, Hennekam, R, Lampe, A, Redeker, E, Homfray, T, Ross, A, Smeland, M, Mansour, S, Parker, M, Cook, J, Splitt, M, Fisher, R, Fryer, A, Magee, A, Wilkie, A, Barnicoat, A
Published 2014Journal article -
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Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism. by Ansari, M, Poke, G, Ferry, Q, Williamson, K, Aldridge, R, Meynert, A, Bengani, H, Chan, C, Kayserili, H, Avci, S, Hennekam, R, Lampe, A, Redeker, E, Homfray, T, Ross, A, Falkenberg Smeland, M, Mansour, S, Parker, M, Cook, J, Splitt, M, Fisher, R, Fryer, A, Magee, A, Wilkie, A, Barnicoat, A
Published 2014Journal article -
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Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations. by Rainger, J, Pehlivan, D, Johansson, S, Bengani, H, Sanchez-Pulido, L, Williamson, K, Ture, M, Barker, H, Rosendahl, K, Spranger, J, Horn, D, Meynert, A, Floyd, J, Prescott, T, Anderson, C, Rainger, J, Karaca, E, Gonzaga-Jauregui, C, Jhangiani, S, Muzny, D, Seawright, A, Soares, D, Kharbanda, M, Murday, V, Finch, A
Published 2014Journal article -
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Validation of the prognostic value of histologic scoring systems in primary sclerosing cholangitis: An international cohort study. by de Vries, E, de Krijger, M, Färkkilä, M, Arola, J, Schirmacher, P, Gotthardt, D, Goeppert, B, Trivedi, P, Hirschfield, G, Ytting, H, Vainer, B, Buuren, H, Biermann, K, Harms, M, Chazouilleres, O, Wendum, D, Kemgang, A, Chapman, R, Wang, L, Williamson, K, Gouw, A, Paradis, V, Sempoux, C, Beuers, U, Hübscher, S, Verheij, J, Ponsioen, C
Published 2016Journal article