Editorial: Pathophysiology of Rare Hemolytic Anemias

von van Wijk, Richard, Bianchi, Paola
Veröffentlicht in Front Physiol (2020)

A Proposed Concept for Defective Mitophagy Leading to Late Stage Ineffective Erythropoiesis in Pyruvate Kinase Deficiency

von van Vuren, Annelies Johanna, van Beers, Eduard Johannes, van Wijk, Richard
Veröffentlicht in Front Physiol (2021)

Red blood cell vesiculation in hereditary hemolytic anemia

von Alaarg, Amr, Schiffelers, Raymond M., van Solinge, Wouter W., van Wijk, Richard
Veröffentlicht 2013

Rare Anemias: Are Their Names Just Smoke and Mirrors?

von Simionato, Greta, van Wijk, Richard, Quint, Stephan, Wagner, Christian, Bianchi, Paola, Kaestner, Lars
Veröffentlicht in Front Physiol (2021)

Liver Iron Retention Estimated from Utilization of Oral and Intravenous Radioiron in Various Anemias and Hemochromatosis in Humans

von van Vuren, Annelies J., van Wijk, Richard, van Beers, Eduard J., Marx, Joannes J.M.
Veröffentlicht in Int J Mol Sci (2020)

Squeezing for Life – Properties of Red Blood Cell Deformability

von Huisjes, Rick, Bogdanova, Anna, van Solinge, Wouter W., Schiffelers, Raymond M., Kaestner, Lars, van Wijk, Richard
Veröffentlicht in Front Physiol (2018)

A Unique Monocyte Transcriptome Discriminates Sickle Cell Disease From Other Hereditary Hemolytic Anemias and Shows the Particular Importance of Lipid and Interferon Signaling

von van Vuren, Annelies J., van Straaten, Stephanie, Mokry, Michal, van Wijk, Richard, van Beers, Eduard J.
Veröffentlicht in Hemasphere (2021)

First description of phosphofructokinase deficiency in spain: identification of a novel homozygous missense mutation in the PFKM gene

von Vives-Corrons, Joan-Lluis, Koralkova, Pavla, Grau, Josep M., Mañú Pereira, Maria del Mar, Van Wijk, Richard
Veröffentlicht 2013

First mutation in the red blood cell-specific promoter of hexokinase combined with a novel missense mutation causes hexokinase deficiency and mild chronic hemolysis

von de Vooght, Karen M.K., van Solinge, Wouter W., van Wesel, Annet C., Kersting, Sabina, van Wijk, Richard
Veröffentlicht 2009

Iron overload in patients with rare hereditary hemolytic anemia: Evidence‐based suggestion on whom and how to screen

von van Straaten, Stephanie, Biemond, Bart J., Kerkhoffs, Jean‐Louis, Gitz‐Francois, Jerney, van Wijk, Richard, van Beers, Eduard J.
Veröffentlicht in Am J Hematol (2018)

The EPO-FGF23 Signaling Pathway in Erythroid Progenitor Cells: Opening a New Area of Research

von van Vuren, Annelies J., Gaillard, Carlo A. J. M., Eisenga, Michele F., van Wijk, Richard, van Beers, Eduard J.
Veröffentlicht in Front Physiol (2019)

Erythrocytosis associated with a novel missense mutation in the HIF2A gene

von van Wijk, Richard, Sutherland, Scott, Van Wesel, Annet C.W., Huizinga, Eric G., Percy, Melanie J., Bierings, Marc, Lee, Frank S.
Veröffentlicht 2010

Red Blood Cells: Chasing Interactions

von Pretini, Virginia, Koenen, Mischa H., Kaestner, Lars, Fens, Marcel H. A. M., Schiffelers, Raymond M., Bartels, Marije, Van Wijk, Richard
Veröffentlicht in Front Physiol (2019)

The Interplay between Drivers of Erythropoiesis and Iron Homeostasis in Rare Hereditary Anemias: Tipping the Balance

von Grootendorst, Simon, de Wilde, Jonathan, van Dooijeweert, Birgit, van Vuren, Annelies, van Solinge, Wouter, Schutgens, Roger, van Wijk, Richard, Bartels, Marije
Veröffentlicht in Int J Mol Sci (2021)

Red blood cell phenotyping from 3D confocal images using artificial neural networks

von Simionato, Greta, Hinkelmann, Konrad, Chachanidze, Revaz, Bianchi, Paola, Fermo, Elisa, van Wijk, Richard, Leonetti, Marc, Wagner, Christian, Kaestner, Lars, Quint, Stephan
Veröffentlicht in PLoS Comput Biol (2021)

Mechanical Stress Induces Ca(2+)-Dependent Signal Transduction in Erythroblasts and Modulates Erythropoiesis

von Aglialoro, Francesca, Abay, Asena, Yagci, Nurcan, Rab, Minke A. E., Kaestner, Lars, van Wijk, Richard, von Lindern, Marieke, van den Akker, Emile
Veröffentlicht in Int J Mol Sci (2021)

The Complexity of Genotype-Phenotype Correlations in Hereditary Spherocytosis: A Cohort of 95 Patients: Genotype-Phenotype Correlation in Hereditary Spherocytosis

von van Vuren, Annelies, van der Zwaag, Bert, Huisjes, Rick, Lak, Nathalie, Bierings, Marc, Gerritsen, Egbert, van Beers, Eduard, Bartels, Marije, van Wijk, Richard
Veröffentlicht in Hemasphere (2019)

Hereditary Xerocytosis due to Mutations in PIEZO1 Gene Associated with Heterozygous Pyruvate Kinase Deficiency and Beta-Thalassemia Trait in Two Unrelated Families

von Fermo, Elisa, Vercellati, Cristina, Marcello, Anna Paola, Zaninoni, Anna, van Wijk, Richard, Mirra, Nadia, Curcio, Cristina, Cortelezzi, Agostino, Zanella, Alberto, Barcellini, Wilma, Bianchi, Paola
Veröffentlicht in Case Rep Hematol (2017)

Successful treatment of fetal hemolytic disease due to glucose phosphate isomerase deficiency (GPI) using repeated intrauterine transfusions: a case report

von Adama van Scheltema, Phebe N, Zhang, Ai, Ball, Lynne M, Steggerda, Sylke J, van Wijk, Richard, Fransen van de Putte, Dietje E, van Kamp, Inge L
Veröffentlicht in Clin Case Rep (2015)

Gene panel sequencing improves the diagnostic work-up of patients with idiopathic erythrocytosis and identifies new mutations

von Camps, Carme, Petousi, Nayia, Bento, Celeste, Cario, Holger, Copley, Richard R., McMullin, Mary Frances, van Wijk, Richard, Ratcliffe, Peter J., Robbins, Peter A., Taylor, Jenny C.
Veröffentlicht in Haematologica (2016)