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Haematologica|March 17, 2018
Proteomic analysis of plasma from children with sickle cell anemia and silent cerebral infarctionSanjay Tewari, George Renney, John Brewin, et al.
British Journal of Haematology|June 27, 2007
The linear effects of alpha-thalassaemia, the UGT1A1 and HMOX1 polymorphisms on cholelithiasis in sickle cell diseaseNisha Vasavda, Stephan Menzel, Sheila Kondaveeti, et al.
Plos One|August 14, 2015
Pulmonary Haemodynamics in Sickle Cell Disease Are Driven Predominantly by a High-Output State Rather Than Elevated Pulmonary Vascular Resistance: A Prospective 3-Dimensional Echocardiography/Doppler StudySitali Mushemi-Blake, Narbeh Melikian, Emma Drasar, et al.
Plos One|June 8, 2018
A survey of genetic fetal-haemoglobin modifiers in Nigerian patients with sickle cell anaemiaTitilope A Adeyemo, Oyesola O Ojewunmi, Idat A Oyetunji, et al.
Blood Advances|October 19, 2018
The platelet NLRP3 inflammasome is upregulated in sickle cell disease via HMGB1/TLR4 and Bruton tyrosine kinaseSebastian Vogel, Taruna Arora, Xunde Wang, et al.
British Journal of Haematology|January 28, 2021
A phenotypic risk score for predicting mortality in sickle cell diseaseVandana Sachdev, Xin Tian, Yuan Gu, et al.
Haematologica|December 23, 2020
Genome wide association study of silent cerebral infarction in sickle cell disease (HbSS and HbSC)John N Brewin, Helen Rooks, Kate Gardner, et al.
British Journal of Haematology|September 28, 2007
Circulating DNA: a potential marker of sickle cell crisisNisha Vasavda, Pinar Ulug, Sheila Kondaveeti, et al.
Blood Advances|March 10, 2022
Genetic variants of PKLR are associated with acute pain in sickle cell diseaseXunde Wang, Kate Gardner, Mickias B Tegegn, et al.
Ebiomedicine|August 29, 2017
Fetal Hemoglobin is Associated with Peripheral Oxygen Saturation in Sickle Cell Disease in TanzaniaSiana Nkya, Josephine Mgaya, Florence Urio, et al.
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