Sickle cell disease in children: chronic complications and search of predictive factors for adverse outcomes

Author:

Silva Inês Vaz1,Reis Ana Filipa2,Palaré Maria João3,Ferrão Anabela3,Rodrigues Teresa4,Morais Anabela3

Affiliation:

1. Department of Paediatrics; Hospital Vila Franca de Xira; Vila Franca de Xira Portugal

2. Department of Paediatrics; Hospital Garcia de Orta; Almada Portugal

3. Unit of Paediatric Haematology; Department of Paediatrics; Hospital de Santa Maria; Centro Hospitalar Lisboa Norte; EPE; Lisboa Portugal

4. Laboratory of Biomathematics; Faculdade de Medicina de Lisboa; Lisboa Portugal

Publisher

Wiley

Subject

Hematology,General Medicine

Reference16 articles.

1. Prevalence of rare diseases: Bibliographic data, Orphanet Report Series, Rare Diseases collection, Nov 2013, Number 1: Listed in alphabetical order of disease or group of diseases http://www.orpha.net/orphacom/cahiers/docs/GB/Prevalence_of_

2. A network model to predict the risk of death in sickle cell disease;Sebastiani;Blood,2007

3. Prognostic significance of early vaso-occlusive complications in children with sickle cell anemia;Quinn;Blood,2007

4. Sickle cell disease: an overview;Ogedegbe;Lab Med,2002

5. Mortality in sickle cell disease. Life expectancy and risk factors for early death in sickle cell disease;Platt;N Engl J Med,1994

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