Literature DB >> 17365983

Sickle cell disease in North Europe.

J Howard1, S C Davies.   

Abstract

The numbers of patients with sickle cell disease in Northern Europe are steadily increasing due to migration, leading to a need for improved healthcare services for these patients. We outline the role of neonatal and antenatal screening programmes in the diagnosis of sickle cell disease, clinical aspects of care and the therapeutic options available. The clinical areas discussed in detail are pain management, the management of stroke and other neurological complications and the management of pulmonary and splenic complications. The role of hydroxyurea, blood transfusion and bone marrow transplantation are also discussed.

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Year:  2007        PMID: 17365983     DOI: 10.1080/00365510601046441

Source DB:  PubMed          Journal:  Scand J Clin Lab Invest        ISSN: 0036-5513            Impact factor:   1.713


  3 in total

1.  Correlating transcranial arterial Doppler velocities with haematologic parameters and haemolytic indices of Nigerian children with sickle cell anaemia.

Authors:  Anas Ismail; Aminu Abba Yusuf; Aisha Kuliya-Gwarzo; Sagir Gumel Ahmed; Abdulkadir Musa Tabari; Shehi Ali Abubakar
Journal:  Ultrasound       Date:  2019-03-09

2.  The challenge of differentiating vaso-occlusive crises from osteomyelitis in children with sickle cell disease and bone pain: A 15-year retrospective review.

Authors:  A Fontalis; K Hughes; M P Nguyen; M Williamson; A Yeo; D Lui; Y Gelfer
Journal:  J Child Orthop       Date:  2019-02-01       Impact factor: 1.548

3.  Hemoglobinopathy prevention in primary care: a reflection of underdetection and difficulties with accessibility of medical care, a quantitative study.

Authors:  Cornelis L Harteveld; Elisa J F Houwink; Margo E van Vliet; Jean-Louis H Kerkhoffs
Journal:  Eur J Hum Genet       Date:  2022-02-25       Impact factor: 5.351

  3 in total

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