Enzymdefekte in Glykolyse und Nukleotidstoffwechsel roter Blutzellen bei nichtsph�rocyt�ren h�molytischen An�mien

Author:

Waller H. D.,Ben�hr H. Chr

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Genetics (clinical),Drug Discovery,Molecular Medicine

Reference191 articles.

1. Akatsuka, J., Nishina, T.: Phosphoglycerate kinase deficiency. Igaku-no-Ayumi83, 638 (1972)

2. Alagille, D., Fleury, J., Odievre, M.: Deficit congenital en 2,3-diphosphoglyceromutase. Bull. Mem. Soc. Med. Hop. Paris115, 493 (1964)

3. Angelman, H., Brain, M.C., MacIver, J.E.: A case of triose phosphate isomerase deficiency with sudden death. Proc. XIII. Int. Congr. Hemat. München 1970, S. 122

4. Arese, P., Bozia, A., Gallo, E., Mazza, U., Pescarmona, G.P.: Red cell glycolysis in a case of 3-phosphoglycerate kinase deficiency. Europ. J. clin. Invest.3, 86 (1973)

5. Arnold, H., Blume, K.G., Busch, D., Lenkeit, U., Löhr, G.W., Lübs, E.: Clinical and biochemical investigations of glucosephosphateisomerase of normal human red cells and in glucosephosphateisomerase deficiency. Klin. Wschr.48, 1299 (1970)

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