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Plos One|October 2, 2010
Experimental generation of SNP haplotype signatures in patients with sickle cell anaemiaStephan Menzel, Jian Qin, Nisha Vasavda, et al.
British Journal of Haematology|September 4, 2008
The presence of alpha-thalassaemia trait blunts the response to hydroxycarbamide in patients with sickle cell diseaseNisha Vasavda, Sheela Badiger, David Rees, et al.
British Journal of Haematology|March 14, 2012
Renal iron load in sickle cell disease is influenced by severity of haemolysisNisha Vasavda, Lucía Gutiérrez, Michael J House, et al.
British Journal of Haematology|February 1, 2011
Blood transfusion usage among adults with sickle cell disease - a single institution experience over ten yearsEmma Drasar, Norris Igbineweka, Nisha Vasavda, et al.
The Journal of Allergy and Clinical Immunology|November 8, 2006
Expression of nonmuscle cofilin-1 and steroid responsiveness in severe asthmaNisha Vasavda, Thomas Eichholtz, Atsushi Takahashi, et al.
Analytical Biochemistry|October 28, 2008
Quantitation of hepcidin in human urine by liquid chromatography-mass spectrometrySukhvinder S Bansal, John M Halket, Adrian Bomford, 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.
Rapid Communications in Mass Spectrometry : RCM|April 29, 2009
Quantification of hepcidin using matrix-assisted laser desorption/ionization time-of-flight mass spectrometrySukhvinder S Bansal, John M Halket, Jane Fusova, et al.
Plos One|September 26, 2015
Tissue Iron Distribution Assessed by MRI in Patients with Iron Loading AnemiasLucía Gutiérrez, Michael J House, Nisha Vasavda, 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.
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