Editorial: Pathophysiology of Rare Hemolytic Anemias

por van Wijk, Richard, Bianchi, Paola
Publicado 2020

Editorial: New Methods for Red Blood Cell Research and Diagnosis

por Bianchi, Paola, van Wijk, Richard
Publicado 2021

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

por van Vuren, Annelies Johanna, van Beers, Eduard Johannes, van Wijk, Richard
Publicado 2021

Red blood cell vesiculation in hereditary hemolytic anemia

por Alaarg, Amr, Schiffelers, Raymond M., van Solinge, Wouter W., van Wijk, Richard
Publicado 2013

Rare Anemias: Are Their Names Just Smoke and Mirrors?

por Simionato, Greta, van Wijk, Richard, Quint, Stephan, Wagner, Christian, Bianchi, Paola, Kaestner, Lars
Publicado 2021

Facilitating EMA binding test performance using fluorescent beads combined with next‐generation sequencing

por Glenthøj, Andreas, Brieghel, Christian, Nardo‐Marino, Amina, van Wijk, Richard, Birgens, Henrik, Petersen, Jesper
Publicado 2021

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

por van Vuren, Annelies J., van Wijk, Richard, van Beers, Eduard J., Marx, Joannes J.M.
Publicado 2020

Squeezing for Life – Properties of Red Blood Cell Deformability

por Huisjes, Rick, Bogdanova, Anna, van Solinge, Wouter W., Schiffelers, Raymond M., Kaestner, Lars, van Wijk, Richard
Publicado 2018

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

por van Vuren, Annelies J., van Straaten, Stephanie, Mokry, Michal, van Wijk, Richard, van Beers, Eduard J.
Publicado 2021

Comment on: Oxygen gradient ektacytometry does not predict pain in children with sickle cell anaemia

por Sheehan, Vivien A., van Beers, Eduard J., Connes, Philippe, van Wijk, Richard, Rab, Minke A. E.
Publicado 2022

PB2509: RED BLOOD CELL PYRUVATE KINASE PROPERTIES IN SICKLE CELL DISEASE – OF MICE AND MEN

por Traets, Marissa, van Oirschot, Brigitte, Levine, Charles, Jans, Judith, Rab, Minke, Chen, Yu-Wei, Van Wijk, Richard
Publicado 2023

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

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

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

por van Straaten, Stephanie, Biemond, Bart J., Kerkhoffs, Jean‐Louis, Gitz‐Francois, Jerney, van Wijk, Richard, van Beers, Eduard J.
Publicado 2018

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

por van Vuren, Annelies J., Gaillard, Carlo A. J. M., Eisenga, Michele F., van Wijk, Richard, van Beers, Eduard J.
Publicado 2019

Red Blood Cells: Chasing Interactions

por Pretini, Virginia, Koenen, Mischa H., Kaestner, Lars, Fens, Marcel H. A. M., Schiffelers, Raymond M., Bartels, Marije, Van Wijk, Richard
Publicado 2019

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

por Grootendorst, Simon, de Wilde, Jonathan, van Dooijeweert, Birgit, van Vuren, Annelies, van Solinge, Wouter, Schutgens, Roger, van Wijk, Richard, Bartels, Marije
Publicado 2021

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

por Simionato, Greta, Hinkelmann, Konrad, Chachanidze, Revaz, Bianchi, Paola, Fermo, Elisa, van Wijk, Richard, Leonetti, Marc, Wagner, Christian, Kaestner, Lars, Quint, Stephan
Publicado 2021

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

por Aglialoro, Francesca, Abay, Asena, Yagci, Nurcan, Rab, Minke A. E., Kaestner, Lars, van Wijk, Richard, von Lindern, Marieke, van den Akker, Emile
Publicado 2021

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

por van Vuren, Annelies, van der Zwaag, Bert, Huisjes, Rick, Lak, Nathalie, Bierings, Marc, Gerritsen, Egbert, van Beers, Eduard, Bartels, Marije, van Wijk, Richard
Publicado 2019

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

por Fermo, Elisa, Vercellati, Cristina, Marcello, Anna Paola, Zaninoni, Anna, van Wijk, Richard, Mirra, Nadia, Curcio, Cristina, Cortelezzi, Agostino, Zanella, Alberto, Barcellini, Wilma, Bianchi, Paola
Publicado 2017