Augsburg-type glucosephosphate isomerase deficiency
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine,Hematology
Link
http://link.springer.com/content/pdf/10.1007/BF01013693.pdf
Reference19 articles.
1. Arnold H, Blume KG, Busch D, Lenkeit U, Löhr GW, Lübs E (1970) Klinische und biochemische Untersuchungen zur Glucosephosphatisomerase normaler menschlicher Erythrozyten und bei Glucosephosphatisomerase-Mangel. Klin Wochenschr 48: 1299?1308
2. Arnold H, Engelhardt R, Löhr GW, Jacobi H, Liebold I (1973) Glucosephosphat-Isomerase Typ Recklinghausen: eine neue Defektvariante mit hämolytischer Anämie. Klin Wochenschr 51: 1198?1204
3. Arnold H, Blume KG, Engelhardt R, Löhr GW (1973) Glucose-phosphate isomerase deficiency: Evidence for in vivo instability of an enzyme variant with hemolysis. Blood 41: 691?699
4. Arnold H, Blume KG, Löhr GW, Schröter W, Koch HH, Wonneberger B (1974) Glucose phosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia: A new variant (type Nordhorn). II. Purification and biochemical properties of the defective enzyme. Pediatr Res 8: 26?30
5. Arnold H (1979) Inherited glucosephospate isomerase deficiency. A review of known variants and some aspects of the pathomechanism of the deficiency. Blut 39: 405?417
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3. GPI Mount Scopus — a variant of glucosephosphate isomerase deficiency;Annals of Hematology;1993-10
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5. Enzyme Activities in Blood Cells of Man and Dogs after Separation on a Discontinuous Percoli Gradient;Enzyme;1983
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