Literature DB >> 4045957

Evaluation of haematological findings in 50 Bahraini patients with sickle cell disease and in some of their parents.

M A Buhazza, A B Bikhazi, F P Khouri.   

Abstract

The haematological findings in 50 Bahrainis with sickle cell disease are reported. This establishes the existence of the Hb S gene in Bahrain. The mean Hb F level in the Bahraini patients was 13.8%, a value lower than that encountered in sickle cell homozygotes from Kuwait and Saudi Arabia.

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Year:  1985        PMID： 4045957      PMCID： PMC1049452          DOI： 10.1136/jmg.22.4.293

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


  10 in total

1.  A rapid method for microelectrophoresis and quantitation of hemoglobins on cellulose acetate.

Authors:  J L GRAHAM; B W GRUNBAUM
Journal:  Am J Clin Pathol       Date:  1963-06       Impact factor: 2.493

2.  Rapid celluose acetate electrophoresis. II. Qualitative and quantitative hemoglobin fractionation.

Authors:  R C BARTLETT
Journal:  Clin Chem       Date:  1963-06       Impact factor: 8.327

3.  Qunatitative determination of the minor hemoglobin component Hb-A2 by DEAE-cellulose chromatography.

Authors:  T H HUISMAN; A M DOZY
Journal:  Anal Biochem       Date:  1961-08       Impact factor: 3.365

4.  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

5.  The human hemoglobins in health and disease.

Authors:  A I CHERNOFF
Journal:  N Engl J Med       Date:  1955-09-01       Impact factor: 91.245

6.  Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.

Authors:  K SINGER; A I CHERNOFF; L SINGER
Journal:  Blood       Date:  1951-05       Impact factor: 22.113

7.  Benign sickle cell disease in Saudi Arabia: survival estimate and population dynamics.

Authors:  A P Gelpi
Journal:  Clin Genet       Date:  1979-04       Impact factor: 4.438

8.  Milder variant of sickle-cell disease in Arabs in Kuwait associated with unusually high level of foetal haemoglobin.

Authors:  S A Ali
Journal:  Br J Haematol       Date:  1970-11       Impact factor: 6.998

9.  Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjects.

Authors:  R P Perrine; M E Pembrey; P John; S Perrine; F Shoup
Journal:  Ann Intern Med       Date:  1978-01       Impact factor: 25.391

10.  Hb F synthesis in sickle cell anaemia: a comparison of Saudi Arab cases with those of African origin.

Authors:  W G Wood; M E Pembrey; G R Serjeant; R P Perrine; D J Weatherall
Journal:  Br J Haematol       Date:  1980-07       Impact factor: 6.998
  10 in total
  1 in total

Review 1.  Sickle cell disease in Middle East Arab countries.

Authors:  Mohsen A F El-Hazmi; Ali M Al-Hazmi; Arjumand S Warsy
Journal:  Indian J Med Res       Date:  2011-11       Impact factor: 2.375
  1 in total

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