Sickle-Cell Disease and Stroke: Quality of Life of Patients in a Chronic Transfusion Regimen from the Caregivers’ Perspective
Author:
Affiliation:
1. Hematology and Hemotherapy Center of Piauí, Teresina, PI, Brazil
2. State University of Piauí, Teresina, PI, Brazil
3. Fernandes Figueira National Institute of Women’s, Children’s and Adolescents’ Health (IFF-FIOCRUZ), Rio de Janeiro, RJ, Brazil
Publisher
Informa UK Limited
Subject
Oncology,Hematology,Pediatrics, Perinatology and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.1080/08880018.2022.2148030
Reference25 articles.
1. Epidemiology and disease burden of sickle cell disease in France: A descriptive study based on a French nationwide claim database
2. Brasil. Ministério da Saúde. Secretaria de Atenção à Saúde. Secretaria de Ciência, Tecnologia e Insumos Estratégicos. Portaria Conjunta no 05, de 19 de fevereiro de 2018. Aprova o Protocolo Clínico e Diretrizes Terapêuticas da Doença Falciforme. Disponível em https://www.gov.br/saude/pt-br/assuntos/protocolos-clinicos-e-diretrizes-terapeuticas-pcdt/arquivos/2018/doenca-falciforme-pcdt.pdf/view. Acessado em 17 de janeiro de 2022]
3. Sickle cell disease: A primary care update
4. Neurologic Complications of Sickle Cell Disease
5. Prevention of a First Stroke by Transfusions in Children with Sickle Cell Anemia and Abnormal Results on Transcranial Doppler Ultrasonography
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