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A Screening Method for Liver Glycogen Diseases

Overview
Journal Arch Dis Child
Specialty Pediatrics
Date 1969 Jun 1
PMID 5254302
Citations 12
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References
1.
OCKERMAN P . The diagnosis of glycogen storage disease in clinical practice. Isr J Med Sci. 1967; 3(3):494-7. View

2.
Hug G . Glucagon tolerance test in glycogen storage disease. J Pediatr. 1962; 60:545-9. DOI: 10.1016/s0022-3476(62)80116-4. View

3.
LOWE C, Sokal J, Mosovich L, Sarcione E, Doray B . Studies in liver glycogen disease. Effects of glucagon and other agents on metabolic pattern and clinical status. Am J Med. 1962; 33:4-19. DOI: 10.1016/0002-9343(62)90272-3. View

4.
HARTMANN Sr A, WOHLTMANN H, PURKERSON M, WESLEY M . Lactate metabolism. Studies of a child with a serious congenital deviation. J Pediatr. 1962; 61:165-80. DOI: 10.1016/s0022-3476(62)80251-0. View

5.
Huijing F . AMYLO-1,6-GLUCOSIDASE ACTIVITY IN NORMAL LEUCOCYTES AND IN LEUCOCYTES OF PATIENTS WITH GLYCOGEN-STORAGE DISEASE. Clin Chim Acta. 1964; 9:269-72. DOI: 10.1016/0009-8981(64)90106-8. View