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Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|September 29, 2007
Hepatic dysfunction in sickle cell disease: a new system of classification based on global assessmentPhilip A Berry, Timothy J S Cross, Swee Lay Thein, et al.
British Journal of Haematology|June 29, 2005
The measurement of urinary hydroxyurea in sickle cell anaemiaR Neil Dalton, Charles Turner, Moira Dick, et al.
British Journal of Haematology|January 6, 2009
Ethnic differences in F cell levels in Jamaica: a potential tool for identifying new genetic loci controlling fetal haemoglobinLisa E Creary, Colin A McKenzie, Stephan Menzel, et al.
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|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.
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