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Items: 20

1.

Challenges of blood transfusions in β-thalassemia.

Shah FT, Sayani F, Trompeter S, Drasar E, Piga A.

Blood Rev. 2019 Sep;37:100588. doi: 10.1016/j.blre.2019.100588. Epub 2019 Jul 6. Review.

2.

Reducing inappropriately suspended VTE prophylaxis through a multidisciplinary shared learning programme and electronic prompting.

Brewer CF, Ip D, Drasar E, Aghakhani P.

BMJ Open Qual. 2019 Mar 1;8(1):e000474. doi: 10.1136/bmjoq-2018-000474. eCollection 2019.

3.

Increased prevalence of renal cysts in patients with sickle cell disease.

Meeks D, Navaratnarajah A, Drasar E, Jaffer O, Wilkins CJ, Thein SL, Sharpe CC.

BMC Nephrol. 2017 Sep 21;18(1):298. doi: 10.1186/s12882-017-0714-3.

4.

Interim assessment of liver damage in patients with sickle cell disease using new non-invasive techniques.

Drasar E, Fitzpatrick E, Gardner K, Awogbade M, Dhawan A, Bomford A, Suddle A, Thein SL.

Br J Haematol. 2017 Feb;176(4):643-650. doi: 10.1111/bjh.14462. Epub 2016 Dec 16.

5.

Survival in adults with sickle cell disease in a high-income setting.

Gardner K, Douiri A, Drasar E, Allman M, Mwirigi A, Awogbade M, Thein SL.

Blood. 2016 Sep 8;128(10):1436-8. doi: 10.1182/blood-2016-05-716910. Epub 2016 Jul 20. No abstract available.

PMID:
27439910
6.

Tissue Iron Distribution Assessed by MRI in Patients with Iron Loading Anemias.

Gutiérrez L, House MJ, Vasavda N, Drašar E, Gonzalez-Gascon Y Marin I, Kulasekararaj AG, St Pierre TG, Thein SL.

PLoS One. 2015 Sep 25;10(9):e0139220. doi: 10.1371/journal.pone.0139220. eCollection 2015.

7.

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 Study.

Mushemi-Blake S, Melikian N, Drasar E, Bhan A, Lunt A, Desai SR, Greenough A, Monaghan MJ, Thein SL, Shah AM.

PLoS One. 2015 Aug 13;10(8):e0135472. doi: 10.1371/journal.pone.0135472. eCollection 2015.

8.

The clinical significance of K-Cl cotransport activity in red cells of patients with HbSC disease.

Rees DC, Thein SL, Osei A, Drasar E, Tewari S, Hannemann A, Gibson JS.

Haematologica. 2015 May;100(5):595-600. doi: 10.3324/haematol.2014.120402. Epub 2015 Mar 6.

9.

Spectral domain optical coherence tomography in patients with sickle cell disease.

Mathew R, Bafiq R, Ramu J, Pearce E, Richardson M, Drasar E, Thein SL, Sivaprasad S.

Br J Ophthalmol. 2015 Jul;99(7):967-72. doi: 10.1136/bjophthalmol-2014-305532. Epub 2015 Jan 16.

PMID:
25595176
10.

Global genetic architecture of an erythroid quantitative trait locus, HMIP-2.

Menzel S, Rooks H, Zelenika D, Mtatiro SN, Gnanakulasekaran A, Drasar E, Cox S, Liu L, Masood M, Silver N, Garner C, Vasavda N, Howard J, Makani J, Adekile A, Pace B, Spector T, Farrall M, Lathrop M, Thein SL.

Ann Hum Genet. 2014 Nov;78(6):434-51. doi: 10.1111/ahg.12077. Epub 2014 Jul 29.

11.

Leucocyte telomere length in patients with sickle cell disease.

Drašar ER, Jiang J, Gardner K, Howard J, Vulliamy T, Vasavda N, Thein SL.

Br J Haematol. 2014 Jun;165(5):725-7. doi: 10.1111/bjh.12776. Epub 2014 Feb 14. No abstract available.

PMID:
24666270
12.

The effect of Duffy antigen receptor for chemokines on severity in sickle cell disease.

Drasar ER, Menzel S, Fulford T, Thein SL.

Haematologica. 2013 Aug;98(8):e87-9. doi: 10.3324/haematol.2013.089243. Epub 2013 Jun 10. No abstract available.

13.

Genetic determinants of haemolysis in sickle cell anaemia.

Milton JN, Rooks H, Drasar E, McCabe EL, Baldwin CT, Melista E, Gordeuk VR, Nouraie M, Kato GR, Minniti C, Taylor J, Campbell A, Luchtman-Jones L, Rana S, Castro O, Zhang Y, Thein SL, Sebastiani P, Gladwin MT; Walk-PHAAST Investigators, Steinberg MH.

Br J Haematol. 2013 Apr;161(2):270-8. doi: 10.1111/bjh.12245. Epub 2013 Feb 14. Erratum in: Br J Haematol. 2014 Aug;166(3):468. Kato, Gregory R [corrected to Kata, Gregory J]. Br J Haematol. 2014 Aug;166(3):468.

14.

Renal iron load in sickle cell disease is influenced by severity of haemolysis.

Vasavda N, Gutiérrez L, House MJ, Drašar E, St Pierre TG, Thein SL.

Br J Haematol. 2012 Jun;157(5):599-605. doi: 10.1111/j.1365-2141.2012.09093.x. Epub 2012 Mar 13.

PMID:
22409346
15.

Serum ferritin and total units transfused for assessing iron overload in adults with sickle cell disease.

Drasar E, Vasavda N, Igbineweka N, Awogbade M, Allman M, Thein SL.

Br J Haematol. 2012 Jun;157(5):645-7. doi: 10.1111/j.1365-2141.2012.09060.x. Epub 2012 Feb 15. Review. No abstract available.

PMID:
22332939
16.

Effects of co-existing α-thalassaemia in sickle cell disease on hydroxycarbamide therapy and circulating nucleic acids.

Vasavda N, Woodley C, Allman M, Drašar E, Awogbade M, Howard J, Thein SL.

Br J Haematol. 2012 Apr;157(2):249-52. doi: 10.1111/j.1365-2141.2011.08937.x. Epub 2011 Nov 15. No abstract available.

PMID:
22082280
17.

Association between hemolysis and albuminuria in adults with sickle cell anemia.

Day TG, Drasar ER, Fulford T, Sharpe CC, Thein SL.

Haematologica. 2012 Feb;97(2):201-5. doi: 10.3324/haematol.2011.050336. Epub 2011 Oct 11.

18.

Changing pattern of hospital admissions of children with sickle cell disease over the last 50 years.

Day TG, Thein SL, Drasar E, Dick MC, Height SE, O'Driscoll S, Rees DC.

J Pediatr Hematol Oncol. 2011 Oct;33(7):491-5. doi: 10.1097/MPH.0b013e31822543f4. Erratum in: J Pediatr Hematol Oncol. 2012 Jan;34(1):78.

PMID:
21941140
19.

Blood transfusion usage among adults with sickle cell disease - a single institution experience over ten years.

Drasar E, Igbineweka N, Vasavda N, Free M, Awogbade M, Allman M, Mijovic A, Thein SL.

Br J Haematol. 2011 Mar;152(6):766-70. doi: 10.1111/j.1365-2141.2010.08451.x. Epub 2011 Jan 31.

PMID:
21275951
20.

Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia.

Makani J, Menzel S, Nkya S, Cox SE, Drasar E, Soka D, Komba AN, Mgaya J, Rooks H, Vasavda N, Fegan G, Newton CR, Farrall M, Thein SL.

Blood. 2011 Jan 27;117(4):1390-2. doi: 10.1182/blood-2010-08-302703. Epub 2010 Nov 10.

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