Three Differing Cases of Glycogen Storage Disease

Author:

Walker D. G.,Ziai M.,Bowman J. E.

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference20 articles.

1. Miscellaneous disorders of metabolism: V. Glycogen storage diseases and galactosaemia;Andersen, D.H.,1957

2. The colorimetric determination of lactic acid in biological material;Barker, S.B.; Summerson, W.H.;J. biol. Chem,1941

3. Biochemical investigation of a case of glycogenstorage disease (von Gierke's disease);Calderbank, A.; Kent, P.W.; Lorber, J.; Manners, D.J.; Wright, A.;Biochem. J,1960

4. Glycogen structure and enzyme deficiencies in glycogen storage disease;T, Cori G.;Harvey Lect,1954

5. Glucose-6-phosphatase of the liver in glycogen storage disease;T., Cori G.; Cori, C.F.;J. biol. Chem,1952

Cited by 3 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. Enzyme patterns in glycogen storage disease type II (Pompe's disease);Metabolism;1966-07

2. Liver glycogen disease in two generations of a family;The American Journal of Medicine;1964-06

3. Medical genetics 1961;Journal of Chronic Diseases;1962-05

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