The burden and quality of life of caregivers of sickle cell anemia patients taking hydroxyurea versus those not taking hydroxyurea
about
Burden and quality of life of mothers of children and adolescents with chronic illnesses: an integrative review.Comment on "The burden and quality of life of caregivers of sickle cell anemia patients taking hydroxyurea versus those not taking hydroxyurea".Family caregiving for adults with sickle cell disease and extremely high hospital use.The impact of the oral condition of children with sickle cell disease on family quality of life.
P2860
The burden and quality of life of caregivers of sickle cell anemia patients taking hydroxyurea versus those not taking hydroxyurea
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2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
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2012年學術文章
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2012年學術文章
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name
The burden and quality of life ...... s those not taking hydroxyurea
@ast
The burden and quality of life ...... s those not taking hydroxyurea
@en
type
label
The burden and quality of life ...... s those not taking hydroxyurea
@ast
The burden and quality of life ...... s those not taking hydroxyurea
@en
prefLabel
The burden and quality of life ...... s those not taking hydroxyurea
@ast
The burden and quality of life ...... s those not taking hydroxyurea
@en
P2093
P2860
P1476
The burden and quality of life ...... s those not taking hydroxyurea
@en
P2093
Albert Schiaveto de Souza
Alexandra Maria Almeida Carvalho Pinto
Elenir Rose Jardim Cury Pontes
Luiz Bernardino Lima da Silva
Maria Lúcia Ivo
Olinda Maria Rodrigues de Araujo
P2860
P304
P356
10.5581/1516-8484.20120070
P577
2012-01-01T00:00:00Z