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Pediatric Blood & Cancer|March 4, 2011
Neurocognitive deficits in children with sickle cell disease: a comprehensive profileChanna T Hijmans, Karin Fijnvandraat, Martha A Grootenhuis, et al.
Expert Review of Hematology|March 27, 2014
Neonatal thrombocytopenia: etiology, management and outcomeSuzanne F Gunnink, Roos Vlug, Karin Fijnvandraat, 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.
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.
British Journal of Haematology|October 11, 2021
Extended phenotyping does not preclude the occurrence of delayed haemolytic transfusion reactions in sickle cell diseaseJorn Gerritsma, Vera Bongaerts, Corien Eckhardt, 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.
Hemoglobin|February 2, 2010
Frequency of the MTHFR C677T polymorphism in Yemeni children with sickle cell diseaseAbdul-Wahab M Al-Saqladi, Greg Harper, Ali Delpisheh, et al.
Frontiers in Digital Health|November 13, 2023
Use of consumer wearables to monitor and predict pain in patients with sickle cell diseaseCaroline Vuong, Kumar Utkarsh, Rebecca Stojancic, et al.
Pediatric Blood & Cancer|March 30, 2023
Efficacy of non-pharmacological interventions to reduce pain in children with sickle cell disease: A systematic reviewSarah van Veelen, Caroline Vuong, Jorn J Gerritsma, et al.
Journal of Thrombosis and Haemostasis : JTH|June 26, 2026
The Diagnosis and Evaluation of Women and Girls with Hemophilia and Hemophilia Carriers: Guidance from the SSC of the ISTHLakshmi Srivaths, Jesus Ardila, Karin Fijnvandraat, et al.
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