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Archives of Disease in Childhood|July 8, 2010
Portacaths are safe for long-term regular blood transfusion in children with sickle cell anaemiaJack L Bartram, Sandra O'Driscoll, Austin G Kulasekararaj, et al.Nature Chemistry|March 24, 2018
Organic synthesis provides opportunities to transform drug discoveryDavid C Blakemore, Luis Castro, Ian Churcher, et al.Bioorganic & Medicinal Chemistry Letters|February 23, 2002
Anionic cyclophanes as potential reversal agents of muscle relaxants by chemical chelationKenneth S Cameron, Lee Fielding, Rona Mason, et al.Blood|December 2, 2006
The effect of deoxygenation on whole-cell conductance of red blood cells from healthy individuals and patients with sickle cell diseaseJoseph A Browning, Henry M Staines, Hannah C Robinson, et al.Journal of Pediatric Hematology/Oncology|September 24, 2011
Changing pattern of hospital admissions of children with sickle cell disease over the last 50 yearsThomas G Day, Swee Lay Thein, Emma Drasar, et al.JIMD Reports|February 22, 2017
An Audit of the Use of Gonadorelin Analogues to Prevent Recurrent Acute Symptoms in Patients with Acute Porphyria in the United KingdomDanja Schulenburg-Brand, Tricia Gardiner, Simon Guppy, et al.British Journal of Haematology|June 22, 2010
Outcome of adults with sickle cell disease admitted to critical care - experience of a single institution in the UKKate Gardner, Cathy Bell, Jack L Bartram, et al.Annals of Hematology|May 21, 2009
Stroke prevention in the young child with sickle cell anaemiaLara Roberts, Sandra O'Driscoll, Moira C Dick, et al.American Journal of Hematology|July 11, 2008
Hydroxyurea therapy lowers circulating DNA levels in sickle cell anemiaPinar Ulug, Nisha Vasavda, Rohan Kumar, et al.British Journal of Haematology|February 22, 2011
Soluble CD163 levels in children with sickle cell diseaseHolger Jon Moller, Marianne Jensby Nielsen, Jack Bartram, et al.Pageof 16