Long-term cornstarch therapy in glycogen storage disease types I, Ib and III
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF01799729
Reference7 articles.
1. Burr, I. N., O'Neall, T. A., Karson, D. B., Howard, L. J. and Green, H. L. Comparison of the effect of total enteral nutrition, continuous intragastric feeding and portocaval shunt on a patient with type I glycogen storage disease.J. Pediatr. 85 (1979) 792
2. Chen, Y. T., Cornblath, M. and Sidbury, T. B. Cornstarch therapy in type I glycogen storage disease.N. Engl. J. Med. 310 (1984) 171
3. Fernandes, J., Berger, R. and Smit, G. P. A. Lactate as a cerebral meta10545c fuel for glucose-6-phosphatase deficient children.Pediatr. Res. 18 (1984a) 335
4. Fernandes, J., Smit, G. P. A. and Berger, R. Dietary treatment of children with liver glycogenosis. In Benson, P. F. (ed.)Screening and Management of Potentially Treatable Genetic Meta10545c Disorders. MTP Press, Lancaster, 1984b, pp. 161–176
5. Greene, H. L., Slonin, A. E., Burr, J. M. and Moran, R. Type I glycogen storage disease: five years of management with nocturnal intragastric feeding.J. Pediatr. 96 (1980) 590
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. Type I glycogen storage disease: Nine years of management with cornstarch;European Journal of Pediatrics;1993-01
2. Pathophysiology and Dietary Treatment of the Glycogen Storage Diseases;Journal of Pediatric Gastroenterology and Nutrition;1990-08
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