The Dr Elizabeth Casson Memorial Lecture 2017: Life as an occupational being von Cox, Diane L

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The opportunities and challenges of implementing our research priorities von Watson, Jo, Cox, Diane L., Cowan, Katherine, Ford, Steve

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Sequence variation database for the Wilson disease copper transporter, ATP7B von Kenney, Susan M, Cox, Diane W

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Survey of UK sonographers on the prevention of work related muscular-skeletal disorder (WRMSD) von Bolton, Gareth C., Cox, Diane L.

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In vivo Reduction of Amyloid-β by a Mutant Copper Transporter von Phinney, Amie L., Drisaldi, Bettina, Schmidt, Stephen D., Lugowski, Stan, Coronado, Veronica, Liang, Yan, Horne, Patrick, Yang, Jing, Sekoulidis, Joannis, Coomaraswamy, Janaky, Chishti, M. Azhar, Cox, Diane W., Mathews, Paul M., Nixon, Ralph A., Carlson, George A., St George-Hyslop, Peter, Westaway, David

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Association of NPAS3 exonic variation with schizophrenia von Macintyre, Georgina, Alford, Tyler, Xiong, Lan, Rouleau, Guy A, Tibbo, Philip G, Cox, Diane W

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Response to the editorial by Dr Geraghty von White, Peter D, Chalder, Trudie, Sharpe, Michael, Angus, Brian J, Baber, Hannah L, Bavinton, Jessica, Burgess, Mary, Clark, Lucy V, Cox, Diane L, DeCesare, Julia C, Goldsmith, Kimberley A, Johnson, Anthony L, McCrone, Paul, Murphy, Gabrielle, Murphy, Maurice, O’Dowd, Hazel, Potts, Laura, Walwyn, Rebacca, Wilks, David

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Three atypical cases of Wilson disease: Assessment of the Leipzig scoring system in making a diagnosis von Xuan, Andy, Bookman, Ian, Cox, Diane W, Heathcote, Jenny

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Alphanumeric Paging: A Potential Source of Problems in Patient Care and Communication von Espino, Sasa, MD, Cox, Diane, MD, Kaplan, Brian, MD

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Intracellular trafficking of the human Wilson protein: the role of the six N-terminal metal-binding sites von Cater, Michael A, Forbes, John, La Fontaine, Sharon, Cox, Diane, Mercer, Julian F B

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Human microphthalmia associated with mutations in the retinal homeobox gene CHX10 von Sarfarazi, Mansoor, McInnes, Roderick R, Ferda Percin, E, Ploder, Lynda A, Yu, Jessica J, Arici, Kemal, Jonathan Horsford, D, Rutherford, Adam, Bapat, Bharati, Cox, Diane W, Duncan, Alessandra M.V, Kalnins, Vitauts I, Kocak-Altintas, Aysegul, Sowden, Jane C, Traboulsi, Elias

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A child with terminal 14q deletion syndrome: Consideration of genotype–phenotype correlations von Schlade‐Bartusiak, Kamilla, Ardinger, Holly, Cox, Diane W.

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The LEC rat has a deletion in the copper transporting ATPase gene homologous to the Wilson disease gene von Wu, Jingshi, Forbes, John R, Chen, Hai Shiene, Cox, Diane W

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Copper transporting P-type ATPases and human disease von Cox, Diane W, Moore, Steven D P

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Functional analysis of mutations in the ATP loop of the Wilson disease copper transporter, ATP7B von Luoma, Leiah M, Deeb, Taha M.M, Macintyre, Georgina, Cox, Diane W

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It's good to talk: auditing clinicians' interactions with patients in a primary care setting von Donnellon, Kay, Hurford, Grace, Cox, Diane L.

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The Wilson disease gene: spectrum of mutations and their consequences von Thomas, Gordon R, Forbes, John R, Roberts, Eve A, Walshe, John M, Cox, Diane W

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A comparison of the mutation spectra of Menkes disease and Wilson disease von HSI, Gloria, COX, Diane W

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Severe hepatic Wilson's disease in preschool-aged children von Wilson, David C., Phillips, M.James, Cox, Diane W., Roberts, Eve A.

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Sequence variation in the ATP‐binding domain of the Wilson disease transporter, ATP7B, affects copper transport in a yeast model system von Hsi, Gloria, Cullen, Lara M., Macintyre, Georgina, Chen, Matthew M., Glerum, D. Moira, Cox, Diane W.

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