Fructose and glucagon loading in siblings with fructose-1,6-diphosphatase deficiency in fed state

Author:

Nagai T.,Yokoyama T.,Hasegawa T.,Tsuchiya Y.,Matsuo N.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference8 articles.

1. Baerlocher K, Gitzelmann R, Nussli R et al (1971). Infantile lactic acidosis due to hereditary fructose-1,6-diphosphatase deficiency.Helv Pediatr Acta 26: 489–506.

2. Baker L, Winegrad AI (1970). Fasting hypoglycemia and metabolic acidosis with deficiency of hepatic fructose-1,6-diphosphatase.Lancet 2: 13–16.

3. Gitzelmann R, Steinmann B, Van den Berghe G (1989). Disorders of fructose metabolism. In Scriver CR, Beaudet AL, Sly WS, Valle D, eds.The Metabolic Basis of Inherited Diseases. 6th Edn. New York: McGraw-Hill, 399–424.

4. Kaufmann U, Froesch ER (1973). Inhibition of phosphorylase-a by fructose-1-phosphate, alpha-glycerophosphate and fructose-1,6-diphosphatase deficiency.Eur J Clin Invest 3: 407–413.

5. Maenpaa PH, Raivio KO, Keromaki MP (1968). Liver adenine nucleotides: Fructose-induced depletion and its effect on protein synthesis.Science 161: 1253–1254.

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