Rob Van Zwieten
Amsterdam, NH, Netherlands
Last Updated: 09/26/2026
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Found 24 publications
Cryopreservation of Red Blood Cells From Sickle Cell Disease Patients for Comparison of Oxygen Gradient Ektacytometry Parameters Between Laboratories to Enable Data Harmonization.
Journal: International journal of laboratory hematology
Published: October 29, 2025
Elevated haemoglobin A1c confounds thalassaemia diagnosis by lowering HbA2 levels.
Journal: Annals of clinical biochemistry
Published: October 27, 2025
Dynamics of neutrophil phenotype and function in sickle cell disease.
Journal: Frontiers in immunology
Published: March 10, 2025
The role of red blood cell characteristics and viscosity in sickle cell retinopathy and maculopathy.
The role of red blood cell characteristics and viscosity in sickle cell retinopathy and maculopathy.
Journal: British journal of haematology
Published: October 28, 2024
Low-dose iron chelation as anti-oxidative therapy in patients with sickle cell disease: A single-centre pilot study.
Journal: British journal of haematology
Published: April 26, 2024
Rapid diagnosis of hereditary haemolytic anaemias using automated rheoscopy and supervised machine learning.
Journal: British journal of haematology
Published: July 07, 2020
Glucose-6-phosphate dehydrogenase deficiency-associated hemolysis and methemoglobinemia in a COVID-19 patient treated with chloroquine.
Journal: American journal of hematology
Published: April 26, 2020
A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic Anemia.
Journal: Hemoglobin
Published: June 14, 2019
Severe hemolytic anemia due to transient acquired G6PD deficiency after ingestion of sodium chlorite.
Journal: Clinical toxicology (Philadelphia, Pa.)
Published: September 21, 2018
Last Updated: 09/26/2026