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Blood Advances|January 4, 2018
Pharmacotherapeutical strategies in the prevention of acute, vaso-occlusive pain in sickle cell disease: a systematic reviewJoep W R Sins, David J Mager, Shyrin C A T Davis, et al.Blood Advances|March 10, 2023
Natural history and rate of progression of retinopathy in adult patients with sickle cell disease: an 11-year follow-up studyRajani P Brandsen, Roselie M H Diederen, Siham Bakhlakh, et al.Annals of Hematology|June 17, 2021
Priapism in patients with hemolytic disorders: a nationwide retrospective cohort studyStinne Tranekær, Dennis Lund Hansen, Bart J Biemond, et al.American Journal of Hematology|January 31, 2024
Neutrophils in sickle cell disease: Exploring their potential role as a therapeutic targetLydian A de Ligt, Aafke E Gaartman, Bart J Biemond, et al.Circulation|January 1, 1996
Comparison of sustained antithrombotic effects of inhibitors of thrombin and factor Xa in experimental thrombosisB J Biemond, P W Friederich, M Levi, et al.Retina (Philadelphia, Pa.)|August 20, 2024
MACULAR NEURODEGENERATIVE AND VASCULAR CHANGES ON OPTICAL COHERENCE TOMOGRAPHIC ANGIOGRAPHY IN SICKLE CELL DISEASE ARE NOT RELATED TO ITS OCULAR AND SYSTEMIC COMPLICATIONSRajani P Brandsen, Bart J Biemond, Gulsum Z Nasim, et al.Journal of Pediatric Hematology/Oncology|May 18, 2021
Mortality and Causes of Death From Sickle Cell Disease in The Netherlands, 1985-2017Eva Rettenbacher, Joëlle Zaal, Harriët Heijboer, et al.Clinical Epidemiology|June 18, 2020
Prevalence of Congenital Hemolytic Disorders in Denmark, 2000-2016Dennis Lund Hansen, Andreas Glenthøj, Sören Möller, et al.The Netherlands Journal of Medicine|June 27, 2013
Chest pain in sickle cell diseaseS H Tonino, E Nur, H M Otten, et al.Journal of Magnetic Resonance Imaging : JMRI|January 25, 2022
Comparative Analysis of Blood T2 Values Measured by T2 -TRIR and TRUSTKoen P A Baas, Bram F Coolen, Esben T Petersen, et al.Pageof 21