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Katugampola, Ruwani P., Anstey, Alexander Vincent, Finlay, Andrew Yule, Whatley, Sharon D., Woolf, Jacqueline, Mason, Nicola G., Deybach, J. C., Puy, H., Ged, C., de Verneuil, H., Hanneken, S., Minder, E., Schneider-Yin, X. and Badminton, Michael Norman 2012. A management algorithm for congenital erythropoietic porphyria derived from a study of 29 cases. British Journal Of Dermatology 167 (4) , pp. 888-900. 10.1111/j.1365-2133.2012.11154.x

Katugampola, Ruwani P., Badminton, Michael Norman, Finlay, Andrew Yule, Whatley, Sharon D., Woolf, Jacqueline, Mason, Nicola G., Deybach, J. C., Puy, H., Ged, C., de Verneuil, H., Hanneken, S., Minder, E., Schneider-Yin, X. and Anstey, Alexander Vincent 2012. Congenital erythropoietic porphyria: A single-observer clinical study of 29 cases. British Journal Of Dermatology 167 (4) , pp. 901-913. 10.1111/j.1365-2133.2012.11160.x

Whatley, Sharon D., Mason, Nicola G., Woolf, Jacqueline, Newcombe, Robert Gordon, Elder, George H. and Badminton, Michael Norman 2009. Diagnostic strategies for autosomal dominant acute porphyrias: retrospective analysis of 467 unrelated patients referred for mutational analysis of the HMBS, CPOX, or PPOX gene. Clinical Chemistry 55 (7) , pp. 1406-1414. 10.1373/clinchem.2008.122564

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