Editorial: Pathophysiology of Rare Hemolytic Anemias

Por van Wijk, Richard, Bianchi, Paola
Publicado no Front Physiol (2020)

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 no Front Physiol (2021)

Red blood cell vesiculation in hereditary hemolytic anemia

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

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 no Int J Mol Sci (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 no 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

Por van Vuren, Annelies J., van Straaten, Stephanie, Mokry, Michal, van Wijk, Richard, van Beers, Eduard J.
Publicado no Hemasphere (2021)

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 em 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

Por de Vooght, Karen M.K., van Solinge, Wouter W., van Wesel, Annet C., Kersting, Sabina, van Wijk, Richard
Publicado em 2009

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 no Am J Hematol (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 no Front Physiol (2019)

Erythrocytosis associated with a novel missense mutation in the HIF2A gene

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

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 no Front Physiol (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 no Int J Mol Sci (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 no 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

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 no Hemasphere (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 no Case Rep Hematol (2017)

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

Por 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
Publicado no Clin Case Rep (2015)

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

Por 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.
Publicado no Haematologica (2016)

Loss-of-function zinc finger mutation in the EGLN1 gene associated with erythrocytosis

Por Sinnema, Margje, Song, Daisheng, Guan, Wei, Janssen, Johanna W. H., van Wijk, Richard, Navalsky, Bradleigh E., Peng, Kai, Donker, Albertine E., Stegmann, Alexander P. A., Lee, Frank S.
Publicado no Blood (2018)

Red Blood Cell Membrane Conductance in Hereditary Haemolytic Anaemias

Por Petkova-Kirova, Polina, Hertz, Laura, Danielczok, Jens, Huisjes, Rick, Makhro, Asya, Bogdanova, Anna, Mañú-Pereira, Maria del Mar, Vives Corrons, Joan-Lluis, van Wijk, Richard, Kaestner, Lars
Publicado no Front Physiol (2019)