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Erythrocytapheresis versus phlebotomy in the initial treatment of HFE hemochromatosis patients: results from a randomized trial.
Rombout-Sestrienkova E, Nieman FH, Essers BA, van Noord PA, Janssen MC, van Deursen CT, Bos LP, Rombout F, van den Braak R, de Leeuw PW, Koek GH. Rombout-Sestrienkova E, et al. Among authors: van noord pa, van den braak r, van deursen ct. Transfusion. 2012 Mar;52(3):470-7. doi: 10.1111/j.1537-2995.2011.03292.x. Epub 2011 Aug 16. Transfusion. 2012. PMID: 21848963 Clinical Trial.
[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. Among authors: van kraaij mg, van deursen ct. Ned Tijdschr Geneeskd. 2012;156(26):A4745. Ned Tijdschr Geneeskd. 2012. PMID: 22759710 Dutch.
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. Among authors: van deursen ct, van kraaij m. Transfusion. 2016 Jan;56(1):261-70. doi: 10.1111/trf.13328. Epub 2015 Sep 10. Transfusion. 2016. PMID: 26358375 Clinical Trial.
A predictive model for estimating the number of erythrocytapheresis or phlebotomy treatments for patients with naïve hereditary hemochromatosis.
Rombout-Sestrienkova E, Winkens B, van Kraaij M, van Deursen CTBM, Janssen MCH, Rennings AMJ, Evers D, Kerkhoffs JL, Masclee A, Koek GH. Rombout-Sestrienkova E, et al. Among authors: van deursen ctbm, van kraaij m. J Clin Apher. 2021 Jun;36(3):340-347. doi: 10.1002/jca.21867. Epub 2020 Dec 24. J Clin Apher. 2021. PMID: 33368569 Free PMC article.
77 results