Glykogenose Typ I mit normaler Aktivität der Glucose-6-Phosphatase in vitro

Author:

Stegner H.,Evert W.,Gaedicke G.

Publisher

Springer Berlin Heidelberg

Reference18 articles.

1. Badouel, J., Lestradet, H v Tichet, J., Sonna, N., Grenet, P.: Glycogenose hepatique sans deficit enzymatique reconnu se compantant cliniquement et biologiquement comme le type I de cori. Ann.Pédiatr. 19, 507 (1972)

2. Bondy, P.K., Felig, P.: Disorders of carbohydrate metabolism. In: Duncan’s diseases of metabolism, Bondy, P.K., Rosenberg, L.E. (eds.). Philadelphia: Saunders 1974

3. Briggs, J.N., Harworth, J.C.: Liver glycogen disease. Report of a case of hyperuricaemia, renal calculi, and no demonstrable enzyme defect. Ann. J. Med. 36, 443 (1964)

4. Bührdel, P., Zimmermann, G., Braun, W., Beyreiss, K.: Zur Klinik und enzymatischen Diagnostik der Glykogenose Typ I. Kinderärztl. Prax. 5, 211 (1977)

5. Chalmers, R.A., Ryman, B.E., Watts, R.W.E.: Studies on a patient with in vivo evidence of Type I glycogenosis and normal enzyme activities in vitro. Acta Paediatr. Scand. 67, 201 (1978)

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Glycogen storage disease type Ib;European Journal of Pediatrics;1983-09

2. Glycogenosis type Ib complicated by severe granulocytopenia resembling inherited neutropenia;European Journal of Pediatrics;1981-09

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