Mechanisms of the acquired erythrocyte enzyme deficiencies in blood diseases
- 1 September 1976
- journal article
- research article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 71 (3), 379-387
- https://doi.org/10.1016/0009-8981(76)90088-7
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Chronic Haemolytic Anaemia in Two Patients Heterozygous for Erythrocyte Pyruvate Kinase DeficiencyScandinavian Journal of Haematology, 1976
- Biochemical characteristics of “young” and “old” erythrocytes of the newborn infantThe Journal of Pediatrics, 1975
- Erythrocyte phosphofructokinase deficiency associated with an unstable variant of muscle phosphofructokinaseClinica Chimica Acta; International Journal of Clinical Chemistry, 1975
- Starch gel electrophoresis of phosphofructokinase in red cellsBiochemical Medicine, 1974
- Enzymatic Activities and Glutathione Content of Erythrocytes in the Newborn: Comparison with Red Cells of Older Normal Subjects and those with Comparable ReticulocytosisActa Haematologica, 1972
- Anomalies of Blood Group Antigens and Erythrocyte Enzymes in Two Types of Chronic Refractory AnaemiaBritish Journal of Haematology, 1969
- Enzymatic basis for the coexistence of myopathy and hemolytic disease in inherited muscle phosphofructokinase deficiencyBiochemical and Biophysical Research Communications, 1969
- Inherited variations in human phosphohexose isomeraseAnnals of Human Genetics, 1968
- Erythrocytenisolierung aus Blut mit BaumwolleKlinische Wochenschrift, 1966
- Phosphofructokinase deficiency in skeletal muscle. A new type of glycogenosisBiochemical and Biophysical Research Communications, 1965