Literature DB >> 13230170

Thalassemia in Jews from Kurdistan.

Y MATOTH, Z SHAMIR, E FREUNDLICH.   

Abstract

Entities:  

Keywords:  ANEMIA, ERYTHROBLASTIC/heredity; HEREDITY

Mesh:

Year:  1955        PMID: 13230170

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


× No keyword cloud information.
  6 in total

1.  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

2.  Haemolytic anaemia in sickle-cell trait.

Authors:  A A CHAZAN; J G MCSORLEY
Journal:  Br Med J       Date:  1956-08-04

3.  [Abnormal human hemoglobin].

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

Review 4.  Diseases of Jews.

Authors:  D M Krikler
Journal:  Postgrad Med J       Date:  1970-12       Impact factor: 2.401

5.  Sodium potassium, water, and haemoglobin in the packed red cells of severe thalassaemia.

Authors:  C CHOREMIS; C ECONOMOU-MAVROU; C TSENGHI
Journal:  J Clin Pathol       Date:  1961-11       Impact factor: 3.411

6.  PLASMA TRAPPING IN THE CENTRIFUGED RED CELLS OF CHILDREN WITH SEVERE THALASSAEMIA.

Authors:  C ECONOMOU-MAVROU; C TSENGHI
Journal:  J Clin Pathol       Date:  1965-03       Impact factor: 3.411

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.