Glucose‐6‐phosphate dehydrogenase deficiency‐associated hemolysis and methemoglobinemia in a COVID‐19 patient treated with chloroquine von Kuipers, Maria T., Zwieten, Rob, Heijmans, Jarom, Rutten, Caroline E., Heer, Koen, Kater, Arnon P., Nur, Erfan

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Analysis of a cohort of 101 CDAII patients: description of 24 new molecular variants and genotype‐phenotype correlations von Bianchi, Paola, Schwarz, Klaus, Högel, Josef, Fermo, Elisa, Vercellati, Cristina, Grosse, Regine, Wijk, Richard, Zwieten, Rob, Barcellini, Wilma, Zanella, Alberto, Heimpel, Hermann

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Rapid diagnosis of hereditary haemolytic anaemias using automated rheoscopy and supervised machine learning von Moura, Pedro L., Dobbe, Johannes G. G., Streekstra, Geert J., Rab, Minke A. E., Veldthuis, Martijn, Fermo, Elisa, van Wijk, Richard, van Zwieten, Rob, Bianchi, Paola, Toye, Ashley M., Satchwell, Timothy J.

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P1450: VOXELOTOR TREATMENT LEADS TO IMPROVED VIABILITY OF SICKLE ERYTHROCYTES von Konté, Kadère, Gaartman, Aafke, Zwieten, Rob, Veldthuis, Martijn, Bruggen, Robin, Biemond, Bart, Nur, Erfan

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The cholesterol content of the erythrocyte membrane is an important determinant of phosphatidylserine exposure von van Zwieten, Rob, Bochem, Andrea E., Hilarius, Petra M., van Bruggen, Robin, Bergkamp, Ferry, Hovingh, G. Kees, Verhoeven, Arthur J.

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Mild dyserythropoiesis and beta-like globin gene expression imbalance due to the loss of histone chaperone ASF1B von Papadopoulos, Petros, Kafasi, Athanassia, De Cuyper, Iris M., Barroca, Vilma, Lewandowski, Daniel, Kadri, Zahra, Veldthuis, Martijn, Berghuis, Jeffrey, Gillemans, Nynke, Benavente Cuesta, Celina Maria, Grosveld, Frank G., van Zwieten, Rob, Philipsen, Sjaak, Vernet, Muriel, Gutierrez, Laura, Patrinos, George P.

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Two novel haemoglobin variants that affect haemoglobin A1c measurement by ion-exchange chromatography von Bots, Michael, Stroobants, An K., Delzenne, Barend, Soeters, Maarten R., de Vries, Johan E., Weykamp, Cas W., Norg, Roelf J.C., Veldthuis, Martijn, Zwieten, Rob van

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Inherited glutathione reductase deficiency and Plasmodium falciparum malaria--a case study von Gallo, Valentina, Schwarzer, Evelin, Rahlfs, Stefan, Schirmer, R Heiner, van Zwieten, Rob, Roos, Dirk, Arese, Paolo, Becker, Katja

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Inborn defects in the antioxidant systems of human red blood cells von van Zwieten, Rob, Verhoeven, Arthur J., Roos, Dirk

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Hemolysis in the spleen drives erythrocyte turnover von Klei, T.R.L, Dalimot, J., Nota, B., Veldthuis, M., Mul, F.P.J, Rademakers, T., Hoogenboezem, M., Nagelkerke, S.Q., van IJcken, W.F.J, Oole, E., Svendsen, P., Moestrup, S.K., van Alphen, F.P.J, Meijer, A.B., Kuijpers, T.W., van Zwieten, R., van Bruggen, R.

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The Effect of Voxelotor on Erythrocyte Deformability, Neutrophil Phenotype and Endothelial Activation von Konté, Kadère, Gaartman, Aafke E., Tanwar, Isha, Beuger, Boukje, Veldthuis, Martijn, Van Zwieten, Rob, van Bruggen, Robin, Biemond, Bart J., Nur, Erfan

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Glucose-6-phosphate dehydrogenase deficiency-associated hemolysis and methemoglobinemia in aCOVID-19 patient treated with chloroquine von Kuipers, Maria T., van Zwieten, Rob, Heijmans, Jarom, Rutten, Caroline E., de Heer, Koen, Kater, Arnon P., Nur, Erfan

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Neutrophil FcγRIIIb Deficiency, Nature, and Clinical Consequences: A Study of 21 Individuals From 14 Families von Haas, Masja de, Kleijer, Marion, Zwieten, Rob van, Roos, Dirk, Borne, Albert E.G.Kr. von dem

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Voxelotor Treatment Leads to Improved Viability of Sickle Erythrocytes and Altered Neutrophil Phenotype von Konté, Kadère, Gaartman, Aafke E., Beuger, Boukje M., Veldthuis, Martijn, van Zwieten, Rob, Van Bruggen, Robin, Biemond, Bart J., Nur, Erfan

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The Rh complex exports ammonium from human red blood cells von Hemker, Mirte B., Cheroutre, Goedele, Van Zwieten, Rob, Maaskant‐van Wijk, Petra A., Roos, Dirk, Loos, Johannes A., Van Der Schoot, C. Ellen, Von Dem Borne, Albert E. G. Kr

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Pleiotropic Effects of Hydroxyurea on Red Blood Cell and Neutrophil Phenotype in Patients with Sickle Cell Disease; Data from the Notice Study von Gaartman, Aafke E., de Ligt, Lydian A., Tool, Anton T.J., Beuger, Boukje M., Veldthuis, Martijn, Kuijpers, Taco W., van Zwieten, Rob, Biemond, Bart J., Van Bruggen, Robin, Nur, Erfan

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Hemolysis in the Spleen Drives Erythrocyte Turnover von Klei, Thomas, Van Bruggen, Robin, Dalimot, Jill, Veldthuis, Martijn, Mul, Erik, Rademakers, Timo, Hoogenboezem, Mark, Nagelkerke, Sietse Quirijn, Van Ijcken, Wilfred, Moestrup, Soren K., van Alphen, Floris, Meijer, Sander, Kuijpers, Taco, van Zwieten, Rob, Svendsen, Pia

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β-globin mutation detection by tagged single-base extension and hybridization to universal glass and flow-through microarrays von VAN MOORSEL, Coline H. M, VAN WIJNGAARDEN, Erwin E, FOKKEMA, Ivo F. A. C, DEN DUNNEN, Johan T, ROOS, Dirk, VAN ZWIETEN, Rob, GIORDANO, Piero C, HARTEVELD, Cornelis L

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Comparison of Spectrophotometry, Chromate Inhibition, and Cytofluorometry Versus Gene Sequencing for Detection of Heterozygously Glucose-6-Phosphate Dehydrogenase-Deficient Females von Peters, Anna L., Veldthuis, Martijn, van Leeuwen, Karin, Bossuyt, Patrick M.M., Vlaar, Alexander P.J., van Bruggen, Robin, de Korte, Dirk, Van Noorden, Cornelis J.F., van Zwieten, Rob

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Partial pyruvate kinase deficiency aggravates the phenotypic expression of band 3 deficiency in a family with hereditary spherocytosis von Zwieten, Rob, Oirschot, Brigitte A., Veldthuis, Martijn, Dobbe, Johannes G., Streekstra, Geert J., Solinge, Wouter W., Schutgens, Roger E.G., Wijk, Richard

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