Rezultati pretrage - van Wijk, Richard

Editorial: Pathophysiology of Rare Hemolytic Anemias od van Wijk, Richard, Bianchi, Paola

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Editorial: New Methods for Red Blood Cell Research and Diagnosis od Bianchi, Paola, van Wijk, Richard

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A Proposed Concept for Defective Mitophagy Leading to Late Stage Ineffective Erythropoiesis in Pyruvate Kinase Deficiency od van Vuren, Annelies Johanna, van Beers, Eduard Johannes, van Wijk, Richard

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Red blood cell vesiculation in hereditary hemolytic anemia od Alaarg, Amr, Schiffelers, Raymond M., van Solinge, Wouter W., van Wijk, Richard

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Rare Anemias: Are Their Names Just Smoke and Mirrors? od Simionato, Greta, van Wijk, Richard, Quint, Stephan, Wagner, Christian, Bianchi, Paola, Kaestner, Lars

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Facilitating EMA binding test performance using fluorescent beads combined with next‐generation sequencing od Glenthøj, Andreas, Brieghel, Christian, Nardo‐Marino, Amina, van Wijk, Richard, Birgens, Henrik, Petersen, Jesper

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Liver Iron Retention Estimated from Utilization of Oral and Intravenous Radioiron in Various Anemias and Hemochromatosis in Humans od van Vuren, Annelies J., van Wijk, Richard, van Beers, Eduard J., Marx, Joannes J.M.

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Squeezing for Life – Properties of Red Blood Cell Deformability od Huisjes, Rick, Bogdanova, Anna, van Solinge, Wouter W., Schiffelers, Raymond M., Kaestner, Lars, van Wijk, Richard

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A Unique Monocyte Transcriptome Discriminates Sickle Cell Disease From Other Hereditary Hemolytic Anemias and Shows the Particular Importance of Lipid and Interferon Signaling od van Vuren, Annelies J., van Straaten, Stephanie, Mokry, Michal, van Wijk, Richard, van Beers, Eduard J.

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Comment on: Oxygen gradient ektacytometry does not predict pain in children with sickle cell anaemia od Sheehan, Vivien A., van Beers, Eduard J., Connes, Philippe, van Wijk, Richard, Rab, Minke A. E.

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First description of phosphofructokinase deficiency in spain: identification of a novel homozygous missense mutation in the PFKM gene od Vives-Corrons, Joan-Lluis, Koralkova, Pavla, Grau, Josep M., Mañú Pereira, Maria del Mar, Van Wijk, Richard

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First mutation in the red blood cell-specific promoter of hexokinase combined with a novel missense mutation causes hexokinase deficiency and mild chronic hemolysis od de Vooght, Karen M.K., van Solinge, Wouter W., van Wesel, Annet C., Kersting, Sabina, van Wijk, Richard

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Iron overload in patients with rare hereditary hemolytic anemia: Evidence‐based suggestion on whom and how to screen od van Straaten, Stephanie, Biemond, Bart J., Kerkhoffs, Jean‐Louis, Gitz‐Francois, Jerney, van Wijk, Richard, van Beers, Eduard J.

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The EPO-FGF23 Signaling Pathway in Erythroid Progenitor Cells: Opening a New Area of Research od van Vuren, Annelies J., Gaillard, Carlo A. J. M., Eisenga, Michele F., van Wijk, Richard, van Beers, Eduard J.

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Erythrocytosis associated with a novel missense mutation in the HIF2A gene od van Wijk, Richard, Sutherland, Scott, Van Wesel, Annet C.W., Huizinga, Eric G., Percy, Melanie J., Bierings, Marc, Lee, Frank S.

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Red Blood Cells: Chasing Interactions od Pretini, Virginia, Koenen, Mischa H., Kaestner, Lars, Fens, Marcel H. A. M., Schiffelers, Raymond M., Bartels, Marije, Van Wijk, Richard

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The Interplay between Drivers of Erythropoiesis and Iron Homeostasis in Rare Hereditary Anemias: Tipping the Balance od Grootendorst, Simon, de Wilde, Jonathan, van Dooijeweert, Birgit, van Vuren, Annelies, van Solinge, Wouter, Schutgens, Roger, van Wijk, Richard, Bartels, Marije

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Red blood cell phenotyping from 3D confocal images using artificial neural networks od Simionato, Greta, Hinkelmann, Konrad, Chachanidze, Revaz, Bianchi, Paola, Fermo, Elisa, van Wijk, Richard, Leonetti, Marc, Wagner, Christian, Kaestner, Lars, Quint, Stephan

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Mechanical Stress Induces Ca(2+)-Dependent Signal Transduction in Erythroblasts and Modulates Erythropoiesis od Aglialoro, Francesca, Abay, Asena, Yagci, Nurcan, Rab, Minke A. E., Kaestner, Lars, van Wijk, Richard, von Lindern, Marieke, van den Akker, Emile

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The Complexity of Genotype-Phenotype Correlations in Hereditary Spherocytosis: A Cohort of 95 Patients: Genotype-Phenotype Correlation in Hereditary Spherocytosis od van Vuren, Annelies, van der Zwaag, Bert, Huisjes, Rick, Lak, Nathalie, Bierings, Marc, Gerritsen, Egbert, van Beers, Eduard, Bartels, Marije, van Wijk, Richard

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