Literature DB >> 13685016

Sickling of erythrocytes in a patient with thalassemia-hemoglobin-I disease.

J ATWATER, I R SCHWARTZ, A J ERSLEV, T L MONTGOMERY, L M TOCANTINS.   

Abstract

Entities:  

Keywords:  ANEMIA, ERYTHROBLASTIC/blood; ANEMIA, SICKLE CELL/case reports; HEMOGLOBIN

Mesh：

Substances：

Year:  1960        PMID： 13685016     DOI： 10.1056/NEJM196012152632402

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


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  11 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.  BETA THALASSEMIA-HEMOGLOBIN D ALPHA. A FAMILY REPORT.

Authors:  R C LEE; T H HUISMAN
Journal:  Am J Hum Genet       Date:  1965-03       Impact factor: 11.025

3.  [Hemoglobin anomalies].

Authors:  K BETKE
Journal:  Blut       Date:  1961

4.  Further studies on the isolation and properties of alpha-chain sub-units of haemoglobin.

Authors:  E R Huehns
Journal:  Biochem J       Date:  1966-12       Impact factor: 3.857

5.  Thalassaemia.

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

6.  An unusual hemoglobin anomaly and its relation to alpha-thalassemia and hemoglobin-H disease.

Authors:  G D Efremov; R N Wrightstone; T H Huisman; W A Schroeder; C Hyman; J Ortega; K Williams
Journal:  J Clin Invest       Date:  1971-08       Impact factor: 14.808

7.  Hb alpha 2glu beta 2 (Hb I) in a Caucasian family: independent mutation of common origin?

Authors:  E W Baur
Journal:  Humangenetik       Date:  1968

8.  Diminished synthesis of an alpha chain mutant, hemoglobin I (alpha-16 lys leads to glu).

Authors:  G J Esan; F J Morgan; J V O'Donnell; S Ford; A Bank
Journal:  J Clin Invest       Date:  1970-12       Impact factor: 14.808

9.  The suppression of haemoglobin E synthesis when hemoglobin H disease and hemoglobin E trait occur together.

Authors:  S Tuchinda; D Beale; H Lehman
Journal:  Humangenetik       Date:  1967

10.  Globin chain synthesis in the alpha thalassemia syndromes.

Authors:  Y W Kan; E Schwartz; D G Nathan
Journal:  J Clin Invest       Date:  1969-11       Impact factor: 14.808
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