Literature DB >> 13404286

Sickle-cell-thalassaemia disease in South Turkey.

M AKSOY, H LEHMANN.   

Abstract

Entities:  

Keywords:  ANEMIA, SICKLE CELL/case reports

Mesh:

Year:  1957        PMID: 13404286      PMCID: PMC1974735          DOI: 10.1136/bmj.1.5021.734

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


× No keyword cloud information.
  11 in total

1.  Studies on abnormal hemoglobins. XI. Sickle cell-thalassemia disease in the Negro; the significance of the S+A+F and S+A patterns obtained by hemoglobin analysis.

Authors:  K SINGER; L SINGER; S R GOLDBERG
Journal:  Blood       Date:  1955-05       Impact factor: 22.113

2.  Sickle-cell trait in South Turkey.

Authors:  M AKSOY
Journal:  Lancet       Date:  1955-03-19       Impact factor: 79.321

3.  A family illustrating the double inheritance of the sickle cell trait and of Mediterranean anaemia.

Authors:  J G HUMBLE; I ANDERSON; J C WHITE; T FREEMAN
Journal:  J Clin Pathol       Date:  1954-08       Impact factor: 3.411

4.  Chronic hemolytic anemia associated with thalassemia and sickling traits.

Authors:  P STURGEON; H A ITANO; W N VALENTINE
Journal:  Blood       Date:  1952-03       Impact factor: 22.113

5.  [Further research on genetics in sickle cell anemia].

Authors:  I GATTO; G PURRAZZELLA
Journal:  Pediatria (Napoli)       Date:  1951 Nov-Dec

6.  Chronic hemolytic anemia in a white child due to thalassemia and sicklemia; with a genealogic survey.

Authors:  C F WASSERMAN; V R PHELPS; A J HERTZOG
Journal:  Pediatrics       Date:  1952-03       Impact factor: 7.124

7.  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

8.  Presence of Foetal Haemoglobin in Cooley's anaemia.

Authors:  A M LIQUORI
Journal:  Nature       Date:  1951-06-09       Impact factor: 49.962

9.  The occurrence in a family of Sicilian ancestry of the traits for both sickling and thalassemia.

Authors:  W N POWELL; J G RODARTE; J V NEEL
Journal:  Blood       Date:  1950-10       Impact factor: 22.113

10.  Sickle cell anemia a molecular disease.

Authors:  L PAULING; H A ITANO
Journal:  Science       Date:  1949-11-25       Impact factor: 47.728

View more
  3 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.  Bibliography of human genetics.

Authors:  R H POST
Journal:  Am J Hum Genet       Date:  1958-06       Impact factor: 11.025

3.  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
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.