Literature DB >> 14071632

HAEMOGLOBIN H DISEASE IN AN ENGLISH FAMILY.

J C WOODROW, R L NOBLE, J H MARTINDALE.   

Abstract

Keywords:  ADOLESCENCE; ANEMIA, HEMOLYTIC; ENGLAND; GENETICS, HUMAN; HEMOGLOBINS, ABNORMAL; SPLENECTOMY; THALASSEMIA

Mesh：

Substances：

Year:  1964        PMID： 14071632      PMCID： PMC1813043          DOI： 10.1136/bmj.1.5374.36

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


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  5 in total

1.  Genetic basis of the thalassaemia diseases.

Authors:  V M INGRAM; A O STRETTON
Journal:  Nature       Date:  1959-12-19       Impact factor: 49.962

2.  Decreased erythrocyte survival in hemoglobin H disease as a result of the abnormal properties of hemoglobin H: the benefit of splenectomy.

Authors:  D A RIGAS; R D KOLER
Journal:  Blood       Date:  1961-07       Impact factor: 22.113

3.  Genetics of haemoglobin H.

Authors:  R D KOLER; D A RIGAS
Journal:  Ann Hum Genet       Date:  1961-05       Impact factor: 1.670

4.  Abnormal human haemoglobins. I. The comparison of normal human and sickle-cell haemoglobins by fingerprinting.

Authors:  V M INGRAM
Journal:  Biochim Biophys Acta       Date:  1958-06

5.  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
  5 in total
  6 in total

1.  Alpha thalassemia: five cases of hemoglobin H disease in three Oriental-Canadian families.

Authors:  R Y Ing; J H Crookston
Journal:  Can Med Assoc J       Date:  1968-07-13       Impact factor: 8.262

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

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

3.  Haemoglobin-H disease presenting with microcytic hypochromic anaemia in an 81 year old woman.

Authors:  O M Jolobe
Journal:  Postgrad Med J       Date:  1993-12       Impact factor: 2.401

4.  Hematologic improvement following splenectomy for hemoglobin-H disease.

Authors:  G M Wagner; S A Liebhaber; H O Cutting; S H Embury
Journal:  West J Med       Date:  1982-10

5.  Family studies of thalassemia in Arabia.

Authors:  J R McNiel
Journal:  Am J Hum Genet       Date:  1967-03       Impact factor: 11.025

6.  Alpha thalassaemia in British people.

Authors:  D R Higgs; H Ayyub; J B Clegg; A V Hill; R D Nicholls; H Teal; J S Wainscoat; D J Weatherall
Journal:  Br Med J (Clin Res Ed)       Date:  1985-05-04
  6 in total

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