Literature DB >> 5015374

Sickle-cell haemoglobin C disease in London.

A J Black, P I Condon, B M Gompels, R L Green, R G Huntsman, G C Jenkins.   

Abstract

The manifestations of the sickling disorders are becoming increasingly familiar to clinicians in Great Britain. One of these disorders, sickle-cell haemoglobin disease, has hitherto received little attention, being regarded as a relatively mild condition. This paper describes some of the distinctive clinical features of the disease as seen in a series of nine cases which have recently presented in London, two of which were fatal. The special hazards of the condition in relation to pregnancy, air travel, and general anaesthesia are discussed.

Mesh:

Year:  1972        PMID: 5015374      PMCID: PMC477220          DOI: 10.1136/jcp.25.1.49

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN: 0021-9746            Impact factor:   3.411


  25 in total

1.  THE COEXISTENCE OF ACUTE RHEUMATIC FEVER AND SICKLE CELL-HEMOGLOBIN C DISEASE.

Authors:  S A LISKER; D FINKELSTEIN; S SCHWARTZ; K MARULYALI; A VALDES-DAPENA
Journal:  Circulation       Date:  1965-01       Impact factor: 29.690

2.  Sickle cell-hemoglobin C disease. Quantitative determination of iron kinetics and hemoglobin synthesis.

Authors:  E R MOVITT; J F MANGUM; W R PORTER
Journal:  Blood       Date:  1963-05       Impact factor: 22.113

3.  The River Niger as a barrier in the spread eastwards of haemoglobin C: a survey of haemoglobins in the lbo.

Authors:  H LEHMANN; C NWOKOLO
Journal:  Nature       Date:  1959-06-06       Impact factor: 49.962

4.  The biophysics of the variants of sickle-cell disease.

Authors:  R C GRIGGS; J W HARRIS
Journal:  AMA Arch Intern Med       Date:  1956-03

5.  Clinical features of the genetic variants of sickle cell disease.

Authors:  E W SMITH; C L CONLEY
Journal:  Bull Johns Hopkins Hosp       Date:  1954-06

6.  Sickle-cell disease and monocular blindness in Africans.

Authors:  F I Konotey-Ahulu
Journal:  Lancet       Date:  1968-07-27       Impact factor: 79.321

7.  Anaesthetic deaths and the sickle-cell trait.

Authors:  F I Konotey-Ahulu
Journal:  Lancet       Date:  1969-02-01       Impact factor: 79.321

8.  Severe crises with jaundice in young non-pregnant adults with sickle-cell haemoglobin-C disease.

Authors:  G Onuaguluchi; E O Akande
Journal:  Lancet       Date:  1966-04-02       Impact factor: 79.321

9.  The management of anaesthesia in sickle cell states.

Authors:  A A Gilbertson; P A Ball; E J Watson-Williams
Journal:  Proc R Soc Med       Date:  1967-07-07

10.  Relatively benign sickle-cell anaemia in 60 patients aged over 30 in the West Indies.

Authors:  G R Serjeant; R Richards; P R Barbor; P F Milner
Journal:  Br Med J       Date:  1968-07-13
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  4 in total

1.  Top-down proteomics and direct surface sampling of neonatal dried blood spots: diagnosis of unknown hemoglobin variants.

Authors:  Rebecca L Edwards; Paul Griffiths; Josephine Bunch; Helen J Cooper
Journal:  J Am Soc Mass Spectrom       Date:  2012-09-20       Impact factor: 3.109

2.  General anaesthesia in sickle-cell disease.

Authors:  J Homi
Journal:  Br Med J       Date:  1979-09-22

3.  Intraoperative death during caesarian section in a patient with sickle-cell trait. The Anaesthesia Advisory Committee to the Chief Coroner of Ontario.

Authors: 
Journal:  Can J Anaesth       Date:  1987-01       Impact factor: 5.063

4.  Hemoglobin variant analysis via direct surface sampling of dried blood spots coupled with high-resolution mass spectrometry.

Authors:  Rebecca L Edwards; Andrew J Creese; Mark Baumert; Paul Griffiths; Josephine Bunch; Helen J Cooper
Journal:  Anal Chem       Date:  2011-02-22       Impact factor: 6.986

  4 in total

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