Pain, quality of life, and coping in sickle cell disease.

Author:

Fuggle P,Shand P A,Gill L J,Davies S C

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference12 articles.

1. Mortality in children and adolescents with sickle cell disease;Leikin, S.L.; Gallagher, D.; Kinney, T.R.;Pediatrics,1989

2. Report on the VIth annual meeting of the WHO working group on the feasibility study of hereditary disease community control programmes (hereditary anaemia);World Health Organisation,1989

3. Sickle cell;Barnhart, M.I.; Henry, R.L.; Lusher, J.M.,1976

4. Psychological adjustment and family functioning in a group of British children with sickle cell disease: preliminary empirical findings, and a meta-analysis. BrJ Clin Psychol;Midence, K.; Fuggle, P.; Davies, S.C.; McManus, C.

5. Psychological and social concomitants of sickle cell anaemia in adolescents;Morgan, S.A.; Jackson, J.;J Pediatr Psychol,1986

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