Factors influencing disease phenotype and penetrance in HFE haemochromatosis von Rochette, J, Le Gac, G, Lassoued, K, Férec, C, Robson, K. J. H

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Elemental mapping of Mg/Ca intensity ratios in marine mollusc shells using laser-induced breakdown spectroscopy von Hausmann, N, Siozos, P, Lemonis, A, Colonese, A. C, Robson, H. K, Anglos, D

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The origin and spread of the HFE-C282Y haemochromatosis mutation von DISTANTE, S, ROBSON, K. J. H, GRAHAM-CAMPBELL, J, ARNAIZ-VILLENA, A, BRISSOT, P, WORWOOD, Mark

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Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer’s disease von Robson, K J H, Lehmann, D J, Wimhurst, V L C, Livesey, K J, Combrinck, M, Merryweather-Clarke, A T, Warden, D R, Smith, A D

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Iron genes, iron load and risk of Alzheimer’s disease von Lehmann, D J, Worwood, M, Ellis, R, Wimhurst, V L J, Merryweather-Clarke, A T, Warden, D R, Smith, A D, Robson, K J H

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A targeted approach significantly increases the identification rate of patients with undiagnosed haemochromatosis von Cadet, E., Capron, D., Perez, A. S., Crépin, S. N., Arlot, S., Ducroix, J.‐P., Dautréaux, M., Fardellone, P., Leflon, P., Merryweather‐Clarke, A. T., Livesey, K. J., Pointon, J. J., Rose, P., Harcourt, J., Emery, J., Sueur, J. M., Feyt, R., Robson, K. J. H., Rochette, J.

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Recent advances in understanding haemochromatosis: a transition state von Robson, K J H, Merryweather-Clarke, A T, Cadet, E, Viprakasit, V, Zaahl, M G, Pointon, J J, Weatherall, D J, Rochette, J

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Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases? von Cadet, E, Capron, D, Gallet, M, Omanga-Léké, M-L, Boutignon, H, Julier, C, Robson, K J H, Rochette, J

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The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading von Livesey, K J, Wimhurst, V L C, Carter, K, Worwood, M, Cadet, E, Rochette, J, Roberts, A G, Pointon, J J, Merryweather-Clarke, A T, Bassett, M L, Jouanolle, A-M, Mosser, A, David, V, Poulton, J, Robson, K J H

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Global prevalence of putative haemochromatosis mutations von Merryweather-Clarke, A T, Pointon, J J, Shearman, J D, Robson, K J

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Multicentric Origin of Hemochromatosis Gene ( HFE) Mutations von Rochette, J., Pointon, J.J., Fisher, C.A., Perera, G., Arambepola, M., Arichchi, D. S. Kodikara, De Silva, S., Vandwalle, J.L., Monti, J.P., Old, J.M., Merryweather-Clarke, A.T., Weatherall, D.J., Robson, K.J.H.

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Thrombospondin related anonymous protein (TRAP) of Plasmodium falciparum binds specifically to sulfated glycoconjugates and to HepG2 hepatoma cells suggesting a role for this molec... von Müller, H.M., Reckmann, I., Hollingdale, M.R., Bujard, H., Robson, K.J., Crisanti, A.

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The effect of HFE mutations on serum ferritin and transferrin saturation in the Jersey population von Merryweather‐Clarke, Alison T., Worwood, Mark, Parkinson, Lisa, Mattock, Chris, Pointon, Jennifer J., Shearman, Jeremy D., Robson, Kathryn J. H.

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Identification of conserved antigenic components for a cytotoxic T lymphocyte-inducing vaccine against malaria von Aidoo, M, Lalvani, A, Allsopp, C.E.M, Plebanski, M, Krausa, P, Browning, M, Gotch, F, Robson, K.J.H, Hill, A.V.S, Meisner, S.J, Morris Jones, S, Greenwood, B.M, Whittle, H.C, Fidock, D.A, Druilhe, P, Takiguchi, M

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New polymorphic microsatellite markers place the haemochromatosis gene telomeric to D6S105 von Raha-Chowdhury, Ruma, Bowen, Derrick J., Stone, Caroline, Pointon, Jennifer J., Terwilliger, Joseph D., Shearman, Jeremy D., Robson, Kathryn J.H., Bomford, Adrian, Worwood, Mark

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Gene symbol: SLC40A1. Disease: Primary iron overload von Zaahl, M G, Merryweather-Clarke, A T, Kotze, M J, van der Merwe, S, Warnich, L, Robson, K J H

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Sequence comparison of rat liver phenylalanine hydroxylase and its cDNA clones von Robson, K. J. H, Beattie, W, James, R. J, Cotton, R. C. H, Morgan, F. J, Woo, S. L. C

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Plasmodium falciparum malaria: the contribution of basic science to treatment and control von Robson, K J. H, Berendt, A R

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DIAGNOSIS AND MANAGEMENT OF HAEMOCHROMATOSIS SINCE THE DISCOVERY OF THE HFE GENE: A EUROPEAN EXPERIENCE von Robson, K J H, Merryweather, A T, Pointon, J J, Shearman, J D

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A rapid non‐invasive method for the detection of the haemochromatosis C282Y mutation von Merryweather‐Clarke, Alison T., Liu, Yan‐Tat, Shearman, Jeremy D., Pointon, Jennifer J., Robson, Kathryn J. H.

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