Full text
PDFImages in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Arnold H., Blume K. G., Busch D., Lenkeit U., Löhr G. W., Lübs E. Klinische und biochemische Untersuchungen zur Glucosephosphatisomerase normaler menschlicher Erythrocyten und bei Glucosephosphatisomerase-Mangel. Klin Wochenschr. 1970 Nov 1;48(21):1299–1308. doi: 10.1007/BF01485522. [DOI] [PubMed] [Google Scholar]
- Baughan M. A., Valentine W. N., Paglia D. E., Ways P. O., Simons E. R., DeMarsh Q. B. Hereditary hemolytic anemia associated with glucosephosphate isomerase (GPI) deficiency--a new enzyme defect of human erythrocytes. Blood. 1968 Aug;32(2):236–249. [PubMed] [Google Scholar]
- Blume K. G., Hryniuk W., Powars D., Trinidad F., West C., Beutler E. Characterization of two new variants of glucose-phosphate-isomerase deficiency with hereditary nonspherocytic hemolytic anemia. J Lab Clin Med. 1972 Jun;79(6):942–949. [PubMed] [Google Scholar]
- Carter N. D., Yoshida A. Purification and characterization of human phosphoglucose isomerase. Biochim Biophys Acta. 1969 May;181(1):12–19. doi: 10.1016/0005-2795(69)90222-0. [DOI] [PubMed] [Google Scholar]
- Dacie J. V., Shinton N. K., Gaffney P. J., Jr, Lehmann H. Haemoglobin Hammersmith (beta-42 (CDI) Phe replaced by ser). Nature. 1967 Nov 18;216(5116):663–665. doi: 10.1038/216663a0. [DOI] [PubMed] [Google Scholar]
- Detter J. C., Ways P. O., Giblett E. R., Baughan M. A., Hopkinson D. A., Povey S., Harris H. Inherited variations in human phosphohexose isomerase. Ann Hum Genet. 1968 May;31(4):329–338. doi: 10.1111/j.1469-1809.1968.tb00565.x. [DOI] [PubMed] [Google Scholar]
- Paglia D. E., Holland P., Baughan M. A., Valentine W. N. Occurrence of defective hexosephosphate isomerization in human erythrocytes and leukocytes. N Engl J Med. 1969 Jan 9;280(2):66–71. doi: 10.1056/NEJM196901092800203. [DOI] [PubMed] [Google Scholar]
- Schröter W., Brittinger G., Zimmerschmitt E., König E., Schrader D. Combined glucosephosphate isomerase and glucose-6-phosphate dehydrogenase deficiency of the erythrocytes: a new haemolytic syndrome. Br J Haematol. 1971 Mar;20(3):249–261. doi: 10.1111/j.1365-2141.1971.tb07036.x. [DOI] [PubMed] [Google Scholar]