Literature DB >> 4266429

[Erythrocytic pyruvate kinase. II. Enzymatic heterogeneity of deficiencies. Studies concerning 28 cases with congenital hemolytic anemia].

P Boivin, C Galand, M C Demartial.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1972        PMID： 4266429

Source DB:  PubMed          Journal:  Nouv Rev Fr Hematol        ISSN： 0029-4810


× No keyword cloud information.
  4 in total

Review 1.  Advances in hereditary red cell enzyme anomalies.

Authors:  A Kahn; J C Kaplan; J C Dreyfus
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

2.  Search for a relationship between molecular anomalies of the mutant erythrocyte pyruvate kinase variants and their pathological expression.

Authors:  A Kahn; J Marie; J L Vives-Corrons; P Maigret; A Najman
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

3.  Hereditary erythrocyte pyruvate-kinase (PK) deficiency and chronic hemolytic anemia: clinical, genetic and molecular studies in six new Spanish patients.

Authors:  J L Vives-Corrons; J Marie; M A Pujades; A Kahn
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

4.  Molecular mechanism of erythrocyte pyruvate kinase deficiency.

Authors:  A Kahn; J Marie; C Galand; P Boivin
Journal:  Humangenetik       Date:  1975-10-07
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.