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Retina (Philadelphia, Pa.)|January 6, 2025
Longitudinal changes of macular neurodegenerative and vascular abnormalities on OCTA in sickle cell diseaseRajani P Brandsen, Bart J Biemond, Erfan Nur, et al.
Haematologica|December 20, 2024
Clinical and laboratory risk factors for sickle cell retinopathy and maculopathy: a scoping review of the current evidenceRajani P Brandsen, Roselie M H Diederen, Gizem Kocabas, et al.
Optics Express|July 20, 2010
Skin color independent assessment of aging using skin autofluorescenceM Koetsier, Erfan Nur, Han Chunmao, et al.
Retina (Philadelphia, Pa.)|April 22, 2025
LONGITUDINAL CHANGES OF MACULAR NEURODEGENERATIVE AND VASCULAR ABNORMALITIES ON OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY IN SICKLE CELL DISEASERajani P Brandsen, Bart J Biemond, Erfan Nur, et al.
British Journal of Haematology|August 4, 2010
Plasma levels of advanced glycation end products are associated with haemolysis-related organ complications in sickle cell patientsErfan Nur, Dees P Brandjes, John-John B Schnog, et al.
Pediatric Blood & Cancer|December 12, 2023
Hoping for a normal life: Decision-making on hematopoietic stem cell transplantation by patients with a hemoglobinopathy and their caregiversHilda Mekelenkamp, Martine de Vries, Ineke Saalmink, et al.
Transplantation and Cellular Therapy|September 19, 2021
Haploidentical Allogeneic Stem Cell Transplantation in Sickle Cell Disease: A Systematic Review and Meta-AnalysisMesire Aydin, Elisabeth Dovern, Mariska M G Leeflang, et al.
British Journal of Haematology|February 20, 2026
Circulating angiogenesis-related biomarkers in sickle cell retinopathy and maculopathyRajani P Brandsen, Ingeborg Klaassen, Renée de Caluwe, et al.
American Journal of Hematology|October 1, 2010
Urinary markers of bone resorption, pyridinoline and deoxypyridinoline, are increased in sickle cell patients with further increments during painful crisisErfan Nur, Willem Mairuhu, Bart J Biemond, et al.
American Journal of Hematology|October 20, 2023
Cerebral hemodynamics and oxygenation in adult patients with sickle cell disease after stem cell transplantationLiza Afzali-Hashemi, Elisabeth Dovern, Koen P A Baas, et al.
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