Literature DB >> 13810006

Persistence of haemoglobin "Bart's" beyond infancy in a child with thalassaemia.

C CHOREMIS, L ZANNOS-MARIOLEA, J A AGER, H LEHMANN.   

Abstract

Entities:  

Keywords:  ANEMIA, ERYTHROBLASTIC; HEMOGLOBIN

Mesh：

Substances：

Year:  1959        PMID： 13810006      PMCID： PMC1991551          DOI： 10.1136/bmj.2.5148.348

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


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  7 in total

1.  THE COEXISTENCE OF THE GENES FOR HEMOGLOBIN E AND ALPHA-THALASSEMIA IN THAIS, WITH RESULTANT SUPPRESSION OF HEMOGLOBIN E SYNTHESIS.

Authors:  S TUCHINDA; D L RUCKNAGEL; V MINNICH; U BOONYAPRAKOB; K BALANKURA; V SUVATEE
Journal:  Am J Hum Genet       Date:  1964-09       Impact factor: 11.025

2.  Haemoglobin 'Barts'--a rare abnormality in the newborn.

Authors:  D H BARROW; H G KOHLER
Journal:  Arch Dis Child       Date:  1960-08       Impact factor: 3.791

3.  The abnormal haemoglobins in haemoglobin-H disease.

Authors:  N DANCE; E R HUEHNS; G H BEAVEN
Journal:  Biochem J       Date:  1963-05       Impact factor: 3.857

4.  Haemoglobin H disease with persistent haemoglobin "Bart's" in an Oriental Jewess and her daughter: a dual alpha-chain deficiency of human haemoglobin.

Authors:  B RAMOT; C SHEBA; S FISHER; J A AGER; H LEHMANN
Journal:  Br Med J       Date:  1959-12-05

5.  Thalassaemia.

Authors:  E R Huehns
Journal:  Postgrad Med J       Date:  1965-12       Impact factor: 2.401

6.  Reaction of haemoglobin alpha-A with haemoglobins beta-A4, gamma-F4 and delta-A2.

Authors:  E R Huehns; G H Beaven; B L Stevens
Journal:  Biochem J       Date:  1964-08       Impact factor: 3.857

7.  [Alpha-thalassemia with HbH and Hb Bart's in a German family].

Authors:  P Rönisch; E Kleihauer
Journal:  Klin Wochenschr       Date:  1967-12-01
  7 in total

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