Annelies J. Van Vuren
Utrecht, UT, Netherlands
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 16 publications
In-depth analysis of osmotic gradient ektacytometry parameters across different genotypes in hereditary spherocytosis.
Journal: British journal of haematology
Published: November 12, 2025
Proton pump inhibition for secondary hemochromatosis in hereditary anemia: a phase III placebo-controlled randomized cross-over clinical trial.
Journal: American journal of hematology
Published: April 07, 2022
Lactate dehydrogenase to carboxyhemoglobin ratio as a biomarker of heme release to heme processing is associated with higher tricuspid regurgitant jet velocity and early death in sickle cell disease.
Journal: American journal of hematology
Published: February 01, 2021
The Interplay between Drivers of Erythropoiesis and Iron Homeostasis in Rare Hereditary Anemias: Tipping the Balance.
Journal: International journal of molecular sciences
Published: January 31, 2021
A Proposed Concept for Defective Mitophagy Leading to Late Stage Ineffective Erythropoiesis in Pyruvate Kinase Deficiency.
Journal: Frontiers in physiology
Published: September 22, 2020
A Unique Monocyte Transcriptome Discriminates Sickle Cell Disease From Other Hereditary Hemolytic Anemias and Shows the Particular Importance of Lipid and Interferon Signaling.
Journal: HemaSphere
Published: March 27, 2020
Liver Iron Retention Estimated from Utilization of Oral and Intravenous Radioiron in Various Anemias and Hemochromatosis in Humans.
Journal: International journal of molecular sciences
Published: January 08, 2020
The Complexity of Genotype-Phenotype Correlations in Hereditary Spherocytosis: A Cohort of 95 Patients: Genotype-Phenotype Correlation in Hereditary Spherocytosis.
Journal: HemaSphere
Published: March 08, 2019
Last Updated: 09/26/2026