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8. Fructose-1,6-diphosphatase deficiency: another enzyme defect which can present itself with the clinical features of "tyrosinosis". Bakker HD; de Bree PK; van Sprang FJ; Wadman SK Clin Chim Acta; 1974 Aug; 55(1):41-7. PubMed ID: 4370029 [No Abstract] [Full Text] [Related]
9. [Recurrent acidosis with hypoglycemia in an infant: fructose-1,6-diphosphatase deficiency]. Fischer PJ; Hecker W Klin Padiatr; 1990; 202(2):73-5. PubMed ID: 2325353 [TBL] [Abstract][Full Text] [Related]
10. Urinary lactate excretion in normal children and in children with enzyme defects of carbohydrate metabolism. Fernandes J; Blom W Clin Chim Acta; 1976 Feb; 66(3):345-52. PubMed ID: 174840 [TBL] [Abstract][Full Text] [Related]
11. Fasting hypoglycaemia and metabolic acidosis associated with deficiency of hepatic fructose-1,6-diphosphatase activity. Baker L; Winegrad AI Lancet; 1970 Jul; 2(7662):13-6. PubMed ID: 4193749 [No Abstract] [Full Text] [Related]
12. Fructose-1,6-diphosphatase deficiency and glyceroluria: one possible etiology for GIS. Beatty ME; Zhang YH; McCabe ER; Steiner RD Mol Genet Metab; 2000 Apr; 69(4):338-40. PubMed ID: 10870852 [TBL] [Abstract][Full Text] [Related]
13. Inhibition of phosphorylase-a by fructose-1-phosphate, alpha-glycerophosphate and fructose-1,6-diphosphate: explanation for fructose-induced hypoglycaemia in hereditary fructose intolerance and fructose-1,6-diphosphatase deficiency. Kaufmann U; Froesch ER Eur J Clin Invest; 1973 Sep; 3(5):407-13. PubMed ID: 4359036 [No Abstract] [Full Text] [Related]