Diagnosis and management of hereditary haemochromatosis by Bokhoven, M A van, Deursen, C Th B M van, Swinkels, D W

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Neuromuscular manifestations in hereditary haemochromatosis by Wouthuis, S. F., van Deursen, C. Th. B. M., te Lintelo, M. P., Rozeman, C. A. M., Beekman, R.

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Does the hepatic iron index differentiate hereditary hemochromatosis from secondary hemochromatosis? by van Deursen, C. Th. B. M., Fickers, M. M. F., Brombacher, P. J., Bassett, Mark

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Erythrocytapheresis versus phlebotomy in the initial treatment of HFE hemochromatosis patients: results from a randomized trial by Rombout-Sestrienkova, Eva, Nieman, Fred H.M., Essers, Brigitte A.B., van Noord, Paulus A.H., Janssen, Mirian C.H., van Deursen, Cees Th.B.M., Bos, Laurens P., Rombout, Ferdinand, van den Braak, Rogier, de Leeuw, Peter W., Koek, Ger H.

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Severe Ankyrin-R deficiency results in impaired surface retention and lysosomal degradation of RhAG in human erythroblasts by Satchwell, Timothy J, Bell, Amanda J, Hawley, Bethan R, Pellegrin, Stephanie, Mordue, Kathryn E, van Deursen, Cees Th B M, Braak, Nicole Heitink-Ter, Huls, Gerwin, Leers, Mathie P G, Overwater, Eline, Tamminga, Rienk Y J, van der Zwaag, Bert, Fermo, Elisa, Bianchi, Paola, van Wijk, Richard, Toye, Ashley M

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Erythrocytapheresis versus phlebotomy in the maintenance treatment of HFE hemochromatosis patients: results from a randomized crossover trial by Rombout-Sestrienkova, Eva, Winkens, Bjorn, Essers, Brigitte A.B., Nieman, Fred H.M., Noord, Paulus A.H., Janssen, Mirian C.H., van Deursen, Cees Th.B.M., Boonen, Annelies, Reuser-Kaasenbrood, Ellen P.J.M., Heeremans, Judith, van Kraaij, Marian, Masclee, Ad, Koek, Ger H.

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Hyperferritinemia and liver iron content determined with MRI: Reintroduction of the liver iron index by Moris, Wenke, Verbeek, Jef, Bakers, Frans C., Rombout-Sestrienkova, Eva, Innocenti, Francesco, Masclee, Ad A.M., Koek, Ger H., van Deursen, Cees Th.B.M.

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Acute heart failure and iron deficiency: a prospective, multicentre, observational study by Dalen, Dirk H., Kragten, Johannes A., Emans, Mireille E., Ofwegen‐Hanekamp, Clara E.E., Klaarwater, Claudia C.R., Spanjers, Mireille H.A., Hendrick, Rémond, Deursen, Cees Th.B.M., Brunner‐La Rocca, Hans‐Peter

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A predictive model for estimating the number of erythrocytapheresis or phlebotomy treatments for patients with naïve hereditary hemochromatosis by Rombout‐Sestrienkova, Eva, Winkens, Bjorn, Kraaij, Marian, Deursen, Cees Th. B. M., Janssen, Mirian C. H., Rennings, Alexander M. J., Evers, Dorothea, Kerkhoffs, Jean‐Louis, Masclee, Ad, Koek, Ger H.

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Severity of iron overload of proband determines serum ferritin levels in families with HFE-related hemochromatosis: The HEmochromatosis FAmily Study by Jacobs, Esther M.G, Hendriks, Jan C.M, van Deursen, Cees Th.B.M, Kreeftenberg, Herman G, de Vries, Richard A, Marx, Joannes J.M, Stalenhoef, Anton F.H, Verbeek, André L.M, Swinkels, Dorine W

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Poster Discussions by Kraßler, J., Meier-Hellmann, A., Bloos, F., Reinhart, K., Heringlake, M., Sehested, J., de Munck, P. B., Rommes, J. H., van Deursen, Th. G. M. A., Bakker, J., Joynt, G. M., Gomersall, C. D., Oh, T. E., Lahtinen, P., Valta, P., Takala, J., de Abreu, M. Gama, Ragaller, M., Quintel, M., Albrecht, D. M.

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