| P2093 | author name string | S. Marstein | |
| P2860 | cites work | Tissue sulfhydryl groups | Q26778486 |
| | Glutathione synthetase deficiency, an inborn error of metabolism involving the gamma-glutamyl cycle in patients with 5-oxoprolinuria (pyroglutamic aciduria). | Q37449843 |
| | The reduction of disulphides by human erythrocytes | Q41960234 |
| | The inhibitory effect at the hexokinase level of disulphides on glucose metabolism in human erythrocytes | Q42553907 |
| | A family with pyroglutamic aciduria (author's transl) | Q44192184 |
| | Pyroglutamic aciduria. Studies in an infant with chronic metabolic acidosis | Q47867627 |
| | Pyroglutamic aciduria--a new inborn error of metabolism | Q48881161 |
| | Glutathione Synthetase Deficiency as a Cause of Hereditary Hemolytic Disease | Q54975433 |
| | Protection of Granulocytes by Vitamin E in Glutathione Synthetase Deficiency | Q66930563 |
| | 5-oxoprolinuria: biochemical observations and case report | Q67587365 |
| | Enzymic method for quantitative determination of nanogram amounts of total and oxidized glutathione: applications to mammalian blood and other tissues | Q68732983 |
| | Disulfide reduction in rat liver. I. Evidence for the presence of nonspecific nucleotide-dependent disulfide reductase and GSH-disulfide transhydrogenase activities in the high-speed supernatant fraction | Q68744280 |
| | Pyroglutamic aciduria (5-oxoprolinuria), an inborn error in glutathione metabolism | Q68794819 |
| | Studies of amino acid content and transport in glutathione-deficient erythrocytes from a patient with pyroglutamic acidemia (5-Oxoprolinemia) | Q72455894 |
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 347-352 | |
| P577 | publication date | 1981-06-01 | |
| P1433 | published in | Scandinavian Journal of Clinical and Laboratory Investigation | Q15760785 |
| P1476 | title | Disulphide reduction in glutathione-deficient erythrocytes from a patient with pyroglutamic acidemia | |
| P478 | volume | 41 | |