Literature DB >> 402762

Quantitation of Hb a2 with DE-52 microchromatography in whole blood as screening test for beta-thalassemia heterozygotes.

R Galanello, M A Melis, P Muroni, A Cao.   

Abstract

HB A2 was assayed by means of DE-52 microchromatography in hemolysates from 285 normal subjects and 223 beta-thalassemia heterozygotes. No overlap was found between both groups. Comparable results were observed analyzing whole blood samples collected in capillary tubes from 550 normal subjects and 295 beta-thalassemia heterozygotes. Our results demonstrate that this technique is useful in a screening program for beta-thalassemia trait.

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Year:  1977        PMID: 402762     DOI: 10.1159/000207857

Source DB:  PubMed          Journal:  Acta Haematol        ISSN: 0001-5792            Impact factor:   2.195


  4 in total

1.  Prevention of homozygous beta-thalassemia by carrier screening and prenatal diagnosis in Sardinia.

Authors:  A Cao; M Furbetta; R Galanello; M A Melis; A Angius; A Ximenes; C Rosatelli; R Ruggeri; M Addis; T Tuveri; A M Falchi; E Paglietti; M T Scalas
Journal:  Am J Hum Genet       Date:  1981-07       Impact factor: 11.025

2.  Thalassaemia types and their incidence in Sardinia.

Authors:  A Cao; R Galanello; M Furbetta; P P Muroni; L Garbato; C Rosatelli; M T Scalas; M Addis; R Ruggeri; L Maccioni; M A Melis
Journal:  J Med Genet       Date:  1978-12       Impact factor: 6.318

Review 3.  Transition of Thalassaemia and Friedreich ataxia from fatal to chronic diseases.

Authors:  Annita Kolnagou; Christina N Kontoghiorghe; George J Kontoghiorghes
Journal:  World J Methodol       Date:  2014-12-26

4.  Haemoglobinopathies in eastern Indian states: a demographic evaluation.

Authors:  Rachana Nagar; Sujata Sinha; Rajiva Raman
Journal:  J Community Genet       Date:  2014-07-25
  4 in total

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