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[Erythrocytapheresis for hereditary haemochromatosis].
Rombout-Sestrienkova E, van Deursen CT, Janssen MC, van Kraaij MG, de Leeuw PW, Koek GH. Rombout-Sestrienkova E, et al. Ned Tijdschr Geneeskd. 2012;156(26):A4745. Ned Tijdschr Geneeskd. 2012. PMID: 22759710 Dutch.
End-stage cardiomyopathy because of hereditary hemochromatosis successfully treated with erythrocytapheresis in combination with left ventricular assist device support.
Rombout-Sestrienkova E, De Jonge N, Martinakova K, Klöpping C, van Galen KP, Vink A, Wajon EM, Smit WM, van Bree C, Koek GH. Rombout-Sestrienkova E, et al. Circ Heart Fail. 2014 May;7(3):541-3. doi: 10.1161/CIRCHEARTFAILURE.114.001198. Circ Heart Fail. 2014. PMID: 24847131 No abstract available.
Erythrocytapheresis versus phlebotomy in the maintenance treatment of HFE hemochromatosis patients: results from a randomized crossover trial.
Rombout-Sestrienkova E, Winkens B, Essers BA, Nieman FH, Noord PA, Janssen MC, van Deursen CT, Boonen A, Reuser-Kaasenbrood EP, Heeremans J, van Kraaij M, Masclee A, Koek GH. Rombout-Sestrienkova E, et al. Transfusion. 2016 Jan;56(1):261-70. doi: 10.1111/trf.13328. Epub 2015 Sep 10. Transfusion. 2016. PMID: 26358375 Clinical Trial.
How we manage patients with hereditary haemochromatosis.
Rombout-Sestrienkova E, van Kraaij MG, Koek GH. Rombout-Sestrienkova E, et al. Br J Haematol. 2016 Dec;175(5):759-770. doi: 10.1111/bjh.14376. Epub 2016 Oct 10. Br J Haematol. 2016. PMID: 27723100 Free article. Review.
15 results