Stephanie Van Straaten
Utrecht, UT, Netherlands
Last Updated: 09/26/2026
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Found 9 publications
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
AG-348 (Mitapivat), an allosteric activator of red blood cell pyruvate kinase, increases enzymatic activity, protein stability, and ATP levels over a broad range of PKLR genotypes.
Journal: Haematologica
Published: September 25, 2019
Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate Kinase Deficiency Natural History Study.
Journal: Haematologica
Published: September 15, 2018
Organ involvement occurs in all forms of hereditary haemolytic anaemia.
Journal: British journal of haematology
Published: September 06, 2018
Iron overload in patients with rare hereditary hemolytic anemia: Evidence-based suggestion on whom and how to screen.
Journal: American journal of hematology
Published: August 08, 2018
Worldwide study of hematopoietic allogeneic stem cell transplantation in pyruvate kinase deficiency.
Worldwide study of hematopoietic allogeneic stem cell transplantation in pyruvate kinase deficiency.
Journal: Haematologica
Published: December 16, 2017
Showing 1-9 of 9
Last Updated: 09/26/2026