Author:
Arnold H.,Dodinval-Versie J.,Lambotte C.,L�hr G. W.,Hofstadt J.
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine,Hematology
Reference10 articles.
1. Arnold, H., Engelhardt, R., Löhr, G. W., Jacobi, H., Liebold, I.: Glucosephosphat-Isomerase Typ Recklinghausen: Eine neue Defectvariante mit hämolytischer Anämie. Klin. Wschr.51, 1198?1204 (1973)
2. Arnold, H., Blume, K.G., Löhr, G.W., Schröter, W., Koch, H.H., Wonneberger, B.: Glucosephosphate isomerase deficiency with congenital nonspherocytic hemolytic anemia: A new variant (Type Nordhorn). II. Purification and biochemical properties of the defective enzyme. Pediat. Res.8, 26?30 (1974)
3. Arnold, H., Blume, K.G., Engelhardt, R., Löhr, G.W.: Glucosephosphate isomerase deficiency: Evidence for in vivo instability of an enzyme variant with hemolysis. Blood41, 691?699 (1973)
4. Arnold, H., Seiberling, M., Blume, K.G., Löhr, G.W.: Immunological studies on glucosephosphate isomerase deficiency Instability and impaired synthesis of the defective enzyme. Klin. Wschr.53, 1135?1136 (1975)
5. Baughan, M.A., Valentine, W.N., Paglia, D.E., Ways, P.R., Simon, E.R., DeMarsh, Q.B.: Hereditary hemolytic anemia associated with glucosephosphate isomerase deficiency-A new enzyme defect of human erythrocytes. Blood30, 550 (1967)
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