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Items: 1 to 20 of 25

1.

Interventions for treating neuropathic pain in people with sickle cell disease.

Asnani MR, Francis DK, Brandow AM, Hammond Gabbadon CE, Ali A.

Cochrane Database Syst Rev. 2019 Jul 5;7:CD012943. doi: 10.1002/14651858.CD012943.pub2. Review.

PMID:
31273755
2.

The additional genetic diagnosis of homozygous sickle cell disease in a patient with Waardenburg-Shah syndrome: a case report.

Rankine-Mullings AE, Serjeant G, Ramsay Z, Hanchard NA, Asnani M.

J Med Case Rep. 2019 Jan 13;13(1):10. doi: 10.1186/s13256-018-1953-z.

3.

Causes of death and early life determinants of survival in homozygous sickle cell disease: The Jamaican cohort study from birth.

Serjeant GR, Chin N, Asnani MR, Serjeant BE, Mason KP, Hambleton IR, Knight-Madden JM.

PLoS One. 2018 Mar 1;13(3):e0192710. doi: 10.1371/journal.pone.0192710. eCollection 2018.

4.

Twelve tips for teaching a comprehensive disease-focused course with a global perspective: A sickle cell disease example.

Bulgin D, Tanabe P, Asnani M, Royal CDM.

Med Teach. 2019 Mar;41(3):275-281. doi: 10.1080/0142159X.2017.1420151. Epub 2018 Jan 15.

5.

Disease Knowledge, Illness Perceptions, and Quality of Life in Adolescents With Sickle Cell Disease: Is There a Link?

Asnani MR, Barton-Gooden A, Grindley M, Knight-Madden J.

Glob Pediatr Health. 2017 Nov 7;4:2333794X17739194. doi: 10.1177/2333794X17739194. eCollection 2017.

6.

Stigma and illness uncertainty: adding to the burden of sickle cell disease.

Blake A, Asnani V, Leger RR, Harris J, Odesina V, Hemmings DL, Morris DA, Knight-Madden J, Wagner L, Asnani MR.

Hematology. 2018 Mar;23(2):122-130. doi: 10.1080/10245332.2017.1359898. Epub 2017 Aug 2. Erratum in: Hematology. 2018 Mar;23(2):i.

PMID:
28766464
7.

Socio-environmental exposures and health outcomes among persons with sickle cell disease.

Asnani MR, Knight Madden J, Reid M, Greene LG, Lyew-Ayee P.

PLoS One. 2017 Apr 6;12(4):e0175260. doi: 10.1371/journal.pone.0175260. eCollection 2017.

8.

Interventions for patients and caregivers to improve knowledge of sickle cell disease and recognition of its related complications.

Asnani MR, Quimby KR, Bennett NR, Francis DK.

Cochrane Database Syst Rev. 2016 Oct 6;10:CD011175. Review.

9.

Increased rates of body dissatisfaction, depressive symptoms, and suicide attempts in Jamaican teens with sickle cell disease.

Bhatt-Poulose K, James K, Reid M, Harrison A, Asnani M.

Pediatr Blood Cancer. 2016 Dec;63(12):2159-2166. doi: 10.1002/pbc.26091. Epub 2016 Jul 9.

PMID:
27393908
10.

Predictors of renal function progression in adults with homozygous sickle cell disease.

Asnani M, Serjeant G, Royal-Thomas T, Reid M.

Br J Haematol. 2016 May;173(3):461-8. doi: 10.1111/bjh.13967. Epub 2016 Mar 27.

PMID:
27018388
11.

'The white blood cell always eat the red': how Jamaicans with sickle cell disease understand their illness.

Anderson M, Asnani M.

Ethn Health. 2016;21(2):103-17. doi: 10.1080/13557858.2015.1028522. Epub 2015 Apr 2.

PMID:
25833758
12.

Renal function in adult Jamaicans with homozygous sickle cell disease.

Asnani MR, Reid ME.

Hematology. 2015 Aug;20(7):422-8. doi: 10.1179/1607845414Y.0000000213. Epub 2014 Nov 28.

PMID:
25431929
13.

Cystatin C: a useful marker of glomerulopathy in sickle cell disease?

Asnani M, Reid M.

Blood Cells Mol Dis. 2015 Jan;54(1):65-70. doi: 10.1016/j.bcmd.2014.07.018. Epub 2014 Oct 6.

PMID:
25300191
14.

Risky behaviours of Jamaican adolescents with sickle cell disease.

Asnani MR, Bhatt K, Younger N, McFarlane S, Francis D, Gordon-Strachan G, Reid ME.

Hematology. 2014 Oct;19(7):373-9. doi: 10.1179/1607845413Y.0000000136. Epub 2013 Nov 25.

PMID:
24165755
15.

Determining glomerular filtration rate in homozygous sickle cell disease: utility of serum creatinine based estimating equations.

Asnani MR, Lynch O, Reid ME.

PLoS One. 2013 Jul 19;8(7):e69922. doi: 10.1371/journal.pone.0069922. Print 2013.

16.

"You just have to live with it": coping with sickle cell disease in Jamaica.

Anderson M, Asnani M.

Qual Health Res. 2013 May;23(5):655-64. doi: 10.1177/1049732313480048. Epub 2013 Mar 4.

PMID:
23459927
17.

Locus of control, depression and quality of life among persons with sickle cell disease in Jamaica.

Gibson RC, Morgan KA, Abel WD, Sewell CA, Martin JS, Lowe GA, Haye Wde L, Edwards CL, O'Garo KN, Reid ME, Asnani MR.

Psychol Health Med. 2013;18(4):451-60. doi: 10.1080/13548506.2012.749353. Epub 2013 Jan 16.

PMID:
23324018
18.

Splenic enlargement in adults with homozygous sickle cell disease: the Jamaican experience.

Asnani MR, Williams A, Reid M.

Hematology. 2013 Jan;18(1):46-9. doi: 10.1179/1607845412Y.0000000036. Epub 2012 Nov 15.

PMID:
23321548
19.

Excess risk of maternal death from sickle cell disease in Jamaica: 1998-2007.

Asnani MR, McCaw-Binns AM, Reid ME.

PLoS One. 2011;6(10):e26281. doi: 10.1371/journal.pone.0026281. Epub 2011 Oct 24.

20.

Higher rates of hemolysis are not associated with albuminuria in Jamaicans with sickle cell disease.

Asnani MR, Fraser RA, Reid ME.

PLoS One. 2011 Apr 14;6(4):e18863. doi: 10.1371/journal.pone.0018863.

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