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Hereditary spectrin deficiency in Golden Retriever dogs.
Slappendel RJ, van Zwieten R, van Leeuwen M, Schneijdenberg CT. Slappendel RJ, et al. Among authors: van leeuwen m, van zwieten r. J Vet Intern Med. 2005 Mar-Apr;19(2):187-92. doi: 10.1892/0891-6640(2005)19<187:hsdigr>2.0.co;2. J Vet Intern Med. 2005. PMID: 15822562 Free article.
A family with complement factor D deficiency.
Biesma DH, Hannema AJ, van Velzen-Blad H, Mulder L, van Zwieten R, Kluijt I, Roos D. Biesma DH, et al. Among authors: van zwieten r, van velzen blad h. J Clin Invest. 2001 Jul;108(2):233-40. doi: 10.1172/JCI12023. J Clin Invest. 2001. PMID: 11457876 Free PMC article.
Hereditary spherocytosis due to band 3 deficiency: 15 novel mutations in SLC4A1.
Van Zwieten R, François JJ, Van Leeuwen K, Van Wesel AC, Van Bruggen R, Van Solinge WW, Roos D, Verhoeven AJ, Van Wijk R. Van Zwieten R, et al. Among authors: van leeuwen k, van bruggen r, van wesel ac, van wijk r, van solinge ww. Am J Hematol. 2013 Feb;88(2):159-60. doi: 10.1002/ajh.23363. Epub 2012 Dec 17. Am J Hematol. 2013. PMID: 23255290 Free article. No abstract available.
Comparison of Spectrophotometry, Chromate Inhibition, and Cytofluorometry Versus Gene Sequencing for Detection of Heterozygously Glucose-6-Phosphate Dehydrogenase-Deficient Females.
Peters AL, Veldthuis M, van Leeuwen K, Bossuyt PMM, Vlaar APJ, van Bruggen R, de Korte D, Van Noorden CJF, van Zwieten R. Peters AL, et al. Among authors: van zwieten r. J Histochem Cytochem. 2017 Nov;65(11):627-636. doi: 10.1369/0022155417730021. Epub 2017 Sep 13. J Histochem Cytochem. 2017. PMID: 28902532 Free PMC article.
Intrinsic defects in erythroid cells from familial hemophagocytic lymphohistiocytosis type 5 patients identify a role for STXBP2/Munc18-2 in erythropoiesis and phospholipid scrambling.
Kostova EB, Beuger BM, Veldthuis M, van der Werff Ten Bosch J, Kühnle I, van den Akker E, van den Berg TK, van Zwieten R, van Bruggen R. Kostova EB, et al. Among authors: van den akker e, van den berg tk, van zwieten r, van der werff ten bosch j, van bruggen r. Exp Hematol. 2015 Dec;43(12):1072-1076.e2. doi: 10.1016/j.exphem.2015.08.007. Epub 2015 Aug 28. Exp Hematol. 2015. PMID: 26320718 Free article. Clinical Trial.
A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic Anemia.
Klei TRL, Kheradmand Kia S, Veldthuis M, Dehbozorgian J, Karimi M, Geissler J, Sellink E, Thiel-Valkhof M, Burger P, van Alphen F, Meijer AB, van Bruggen R, van Zwieten R. Klei TRL, et al. Among authors: van zwieten r. Hemoglobin. 2019 Mar;43(2):77-82. doi: 10.1080/03630269.2019.1601107. Epub 2019 Jun 13. Hemoglobin. 2019. PMID: 31190578
59 results