Literature DB >> 4642791

Benign obstetric history in women with sickle-cell anaemia associated with -thalassaemia.

A van Enk, A Lang, J M White, H Lehmann.   

Abstract

Two Ghanaian women with sickle-cell anaemia and alpha-thalassaemia were found to have an unusually benign obstetric history. In addition to two factors present which are known to moderate the clinical course of sickle-cell anaemia, good socioeconomic status and a relatively high Hb F level, it is suggested that alpha-thalassaemia may act among other things by lowering the haemoglobin concentration in the red cells and thereby lowering their tendency to sickle in vivo.

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Year:  1972        PMID: 4642791      PMCID: PMC1788764          DOI: 10.1136/bmj.4.5839.524

Source DB:  PubMed          Journal:  Br Med J        ISSN: 0007-1447


  14 in total

1.  Amelioration of sickle cell disease by persistent fetal hemoglobin.

Authors:  J F JACKSON; J L ODOM; W N BELL
Journal:  JAMA       Date:  1961-09-23       Impact factor: 56.272

2.  Intraerythrocytic precipitations of haemoglobins S and C.

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Journal:  Nat New Biol       Date:  1972-01-19

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Authors:  K Nierhaus; K Betke
Journal:  Klin Wochenschr       Date:  1968-01-01

4.  A new sickling disorder resulting from interaction of the genes for haemoglobin S and alpha-thalassaemia.

Authors:  D J Weatherall; J B Clegg; J Blankson; J R McNeil
Journal:  Br J Haematol       Date:  1969-12       Impact factor: 6.998

5.  Abnormal haemoglobins in Zambia. A new haemoglobin Zambia alpha-60 (E9) lysine--asparagine.

Authors:  G P Barclay; D Charlesworth; H Lehmann
Journal:  Br Med J       Date:  1969-12-06

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Authors:  A J Marengo-Rowe
Journal:  J Clin Pathol       Date:  1965-11       Impact factor: 3.411

7.  Studies on the heterogeneity of hemoglobin. IX. The use of Tris(hydroxymethyl)aminomethanehcl buffers in the anion-exchange chromatography of hemoglobins.

Authors:  T H Huisman; A M Dozy
Journal:  J Chromatogr       Date:  1965-07

8.  Characterization of alpha23GluNH2 in hemoglobin Memphis. Hemoglobin Memphis/S, a new variant of molecular disease.

Authors:  L M Kraus; T Miyaji; I Iuchi; A P Kraus
Journal:  Biochemistry       Date:  1966-11       Impact factor: 3.162

9.  -thalassemia in the American Negro.

Authors:  E Schwartz; J Atwater
Journal:  J Clin Invest       Date:  1972-02       Impact factor: 14.808

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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  7 in total

1.  Haemoglobinopathies in pregnancy.

Authors:  R G Huntsman
Journal:  J Clin Pathol Suppl (R Coll Pathol)       Date:  1976

2.  On the nature of sickle-cell disease in the Arabian Peninsula.

Authors:  M A El-Hazmi
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

3.  Heterogeneity of sickle-cell anemia based on a profile of hematological variables.

Authors:  D J Odenheimer; C F Whitten; D L Rucknagel; S A Sarnaik; C F Sing
Journal:  Am J Hum Genet       Date:  1983-11       Impact factor: 11.025

4.  Alpha thalassemia among sickle cell anaemia patients in Kampala, Uganda.

Authors:  Irene Lubega; Christopher M Ndugwa; Edison A Mworozi; James K Tumwine
Journal:  Afr Health Sci       Date:  2015-06       Impact factor: 0.927

5.  Sickle cell disease in Saudi Arabs in early childhood.

Authors:  R P Perrine; P John; M Pembrey; S Perrine
Journal:  Arch Dis Child       Date:  1981-03       Impact factor: 3.791

6.  Lack of influence of fetal hemoglobin levels or erythrocyte indices on the severity of sickle cell anemia.

Authors:  D R Powars; W A Schroeder; J N Weiss; L S Chan; S P Azen
Journal:  J Clin Invest       Date:  1980-03       Impact factor: 14.808

7.  Modification of hemoglobin H disease by sickle trait.

Authors:  K K Matthay; W C Mentzer; A M Dozy; Y W Kan; D F Bainton
Journal:  J Clin Invest       Date:  1979-10       Impact factor: 14.808

  7 in total

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