Literature DB >> 14363321

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.

K SINGER, L SINGER, S R GOLDBERG.   

Abstract

Entities:  

Keywords:  ANEMIA, ERYTHROBLASTIC; ANEMIA, SICKLE CELL; HEMOGLOBIN/diseases

Mesh:

Substances:

Year:  1955        PMID: 14363321

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


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  7 in total

Review 1.  HUMAN HAEMOGLOBINS.

Authors:  E R HUEHNS; E M SHOOTER
Journal:  J Med Genet       Date:  1965-03       Impact factor: 6.318

2.  Hereditary elliptocytosis. Study of a Turkish family.

Authors:  A I CETINGIL; M AKSOY
Journal:  Blut       Date:  1962-04

3.  The sickle cell disease: current status and preliminary research observations.

Authors:  H W KENNEY; R T SMOOT; J D TRADER; C R DOWE; C C ALLAIN
Journal:  J Natl Med Assoc       Date:  1961-03       Impact factor: 1.798

4.  Studies on the destruction of red blood cells. XII. Factors influencing the role of S hemoglobin in the pathologic physiology of sickle cell anemia and related disorders.

Authors:  M S GREENBERG; E H KASS; W B CASTLE
Journal:  J Clin Invest       Date:  1957-06       Impact factor: 14.808

5.  Sickle-cell-thalassaemia disease in South Turkey.

Authors:  M AKSOY; H LEHMANN
Journal:  Br Med J       Date:  1957-03-30

6.  Sickle-cell trait and malaria in Africa.

Authors:  G M EDINGTON; H LEHMANN
Journal:  Bull World Health Organ       Date:  1956       Impact factor: 9.408

7.  [Abnormal human hemoglobin].

Authors:  K BETKE
Journal:  Klin Wochenschr       Date:  1956-02-01
  7 in total

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