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Computer and mobile technology interventions to promote medication adherence and disease management in people with thalassemia

BACKGROUND: Thalassemia syndromes are inherited hemoglobin disorders that result when the synthesis of normal hemoglobin is lacking or significantly reduced. For people with thalassemia, long‐term red blood cell transfusion remains the mainstay of therapy, which may lead to iron overload causing sev...

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Dettagli Bibliografici
Pubblicato in:Cochrane Database Syst Rev
Autori principali: Badawy, Sherif M, Morrone, Kerry, Thompson, Alexis, Palermo, Tonya M
Natura: Artigo
Lingua:Inglês
Pubblicazione: John Wiley & Sons, Ltd 2019
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6598413/
https://ncbi.nlm.nih.gov/pubmed/31250923
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/14651858.CD012900.pub2
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