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Environmental determinants of severity in sickle cell diseaseThe clinical significance of K-Cl cotransport activity in red cells of patients with HbSC diseaseSpinal versus general anesthesia for Cesarean section in patients with sickle cell anemia.A validated measure of adherence to antibiotic prophylaxis in children with sickle cell disease.Community engagement to inform the development of a sickle cell counselor training and certification program in GhanaGene therapy for monogenic disorders of the bone marrow.Sickle cell disease in adults: developing an appropriate care planThe significance of inadequate transcranial Doppler studies in children with sickle cell disease.Sickle cell disease: Status with particular reference to India.Dynamics of von Willebrand factor reactivity in sickle cell disease during vaso-occlusive crisis and steady state.Vitamin D deficiency and its correction in children with sickle cell anaemia.Challenges of vascular access in red cell exchange in sickle cell patients.Proteomic analysis of plasma from children with sickle cell anemia and silent cerebral infarction.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Management of sickle cell disease in the community.
@en
type
label
Management of sickle cell disease in the community.
@en
prefLabel
Management of sickle cell disease in the community.
@en
P2860
P356
P1433
P1476
Management of sickle cell disease in the community.
@en
P2093
Valentine Brousse
P2860
P356
10.1136/BMJ.G1765
P407
P577
2014-03-10T00:00:00Z