The role of religious leaders and faith organisations in haemoglobinopathies: a review

Author:

Toni-Uebari Thelma K,Inusa Baba PD

Publisher

Springer Science and Business Media LLC

Subject

Hematology,Molecular Biology

Reference32 articles.

1. WHO: Sickle-cell disease and other haemoglobin disorders, Fact sheet N°308. [ http://www.who.int/mediacentre/factsheets/fs308/en/ ]

2. Anie KA, Steptoe A, Ball S, Dick M, Smalling BM: Coping and health service utilisation in a UK study of paediatric sickle cell pain. Arch Dis Child. 2002, 86: 325-329. 10.1136/adc.86.5.325.

3. Lucas SB, Mason DG, Mason M, Weyman D: A Sickle Crisis? A report of the National Confidential Enquiry into Patient Outcome and Death. London. 2008, [ http://www.ncepod.org.uk/2008report1/Downloads/Sickle_report.pdf ]

4. Sickle cell disease in childhood: Standards and guidelines for clinical care, NHS Sickle Cell and Thalassaemia Screening Programme. [ http://sct.screening.nhs.uk/cms.php?folder=2493#fileid10762 ]

5. Streetly A, Latinovic R, Hall K, Henthorn J: Implementation of universal newborn bloodspot screening for sickle cell disease and other clinically significant haemoglobinopathies in England: screening results for 2005–7. Journal of Clinical Pathology. 2009, 62 (1): 26-30. 10.1136/jcp.2008.058859.

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