Literature DB >> 23049434

Comment on "The burden and quality of life of caregivers of sickle cell anemia patients taking hydroxyurea versus those not taking hydroxyurea".

José Carlos Souza1, Jucimara Zacarias M Silveira.   

Abstract

Entities:  

Year:  2012        PMID： 23049434      PMCID： PMC3460403          DOI： 10.5581/1516-8484.20120064

Source DB:  PubMed          Journal:  Rev Bras Hematol Hemoter        ISSN： 1516-8484


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  3 in total

Review 1.  [Quality of life and health: conceptual and methodological issues].

Authors:  Eliane Maria Fleury Seidl; Célia Maria Lana da Costa Zannon
Journal:  Cad Saude Publica       Date:  2004-04-06       Impact factor: 1.632

2.  The World Health Organization Quality of Life assessment (WHOQOL): position paper from the World Health Organization.

Authors: 
Journal:  Soc Sci Med       Date:  1995-11       Impact factor: 4.634

3.  The burden and quality of life of caregivers of sickle cell anemia patients taking hydroxyurea versus those not taking hydroxyurea.

Authors:  Luiz Bernardino Lima da Silva; Maria Lúcia Ivo; Albert Schiaveto de Souza; Elenir Rose Jardim Cury Pontes; Alexandra Maria Almeida Carvalho Pinto; Olinda Maria Rodrigues de Araujo
Journal:  Rev Bras Hematol Hemoter       Date:  2012
  3 in total

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