Literature DB >> 6799049

Survey of sickle-cell disease in England and Wales.

L R Davis, E R Huehns, J M White.   

Abstract

The incidence and the clinical course of patients suffering from sickle-cell syndrome (Hb SS; Hb SC; Hb S thal) in England and Wales are not known. In 1979 an ad hoc committee was formed to investigate these problems. Initially, a questionnaire was sent to 227 haematologists in England and Wales to determine the number of cases in these countries. The replies have indicated that 1367 cases were seen in 1978 and 1979. Probably this may represent only half the total number of cases. From this survey it has been possible to draw up a composite map showing the location of patients, which has provided a basis to determine the clinical course of the disease, and for further studies into the complications and management of sickle-cell disease in England and Wales. From a second questionnaire preliminary data about the general management and mortality in England and Wales have been recorded.

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Year:  1981        PMID: 6799049      PMCID: PMC1507884          DOI: 10.1136/bmj.283.6305.1519

Source DB:  PubMed          Journal:  Br Med J (Clin Res Ed)        ISSN: 0267-0623


  6 in total

1.  Natural history of sickle cell disease--the first ten years.

Authors:  D R Powars
Journal:  Semin Hematol       Date:  1975-07       Impact factor: 3.851

2.  Deaths in children with sickle cell anemia. A clinical analysis of 19 fatal instances in Chicago.

Authors:  R A Seeler
Journal:  Clin Pediatr (Phila)       Date:  1972-11       Impact factor: 1.168

3.  Effect of introducing antenatal diagnosis on reproductive behaviour of families at risk for thalassaemia major.

Authors:  B Modell; R H Ward; D V Fairweather
Journal:  Br Med J       Date:  1980-06-07

4.  Sickle cell haemoglobinopathies in England.

Authors:  J R Mann
Journal:  Arch Dis Child       Date:  1981-09       Impact factor: 3.791

5.  Admissions to hospital of children with sickle-cell anaemia: a study in south London.

Authors:  L N Murtaza; C E Stroud; L R Davis; D J Cooper
Journal:  Br Med J (Clin Res Ed)       Date:  1981-03-28

6.  Sickle-cell disease in a British urban community.

Authors:  E Anionwu; D Walford; M Brozović; B Kirkwood
Journal:  Br Med J (Clin Res Ed)       Date:  1981-01-24
  6 in total
  7 in total

1.  Gall stones in sickle cell disease in the United Kingdom.

Authors:  L R Bond; S R Hatty; M E Horn; M Dick; H B Meire; A J Bellingham
Journal:  Br Med J (Clin Res Ed)       Date:  1987-07-25

2.  Neonatal screening for sickle cell diseases in Camberwell: results and recommendations of a two year pilot study.

Authors:  M E Horn; M C Dick; B Frost; L R Davis; A J Bellingham; C E Stroud; J W Studd
Journal:  Br Med J (Clin Res Ed)       Date:  1986-03-15

3.  Paediatrics among ethnic minorities. Afro-Caribbean and African families.

Authors:  J Black
Journal:  Br Med J (Clin Res Ed)       Date:  1985-03-30

4.  Acute admissions of patients with sickle cell disease who live in Britain.

Authors:  M Brozović; S C Davies; A I Brownell
Journal:  Br Med J (Clin Res Ed)       Date:  1987-05-09

5.  Bone disorders in sickle-cell disease.

Authors:  O Onuba
Journal:  Int Orthop       Date:  1993-12       Impact factor: 3.075

6.  Sickle cell disease in Britain.

Authors:  M Brozović; E Anionwu
Journal:  J Clin Pathol       Date:  1984-12       Impact factor: 3.411

7.  Exchange transfusion in life-threatening sickling crises.

Authors:  J E Van de Pette; T C Pearson; N G Slater
Journal:  J R Soc Med       Date:  1982-10       Impact factor: 18.000

  7 in total

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