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12. Infantile lactic acidosis due to hereditary fructose 1,6-diphosphatase deficiency. Baerlocher K, Gitzelmann R, Nüssli R, Dumermuth G. Helv Paediatr Acta; 1971 Dec 13; 26(5):489-506. PubMed ID: 4335192 [No Abstract] [Full Text] [Related]
13. [Baker-Winegrad disease (hepatomegaly, hypoglycemia during fasting, hyperlactacidemic metabolic acidosis, hepatic fructose-1-6-diphosphatase deficiency). Presentation of the 1st Italian case and pathogenetic hypothesis]. De Prà M, Laudanna E. Minerva Pediatr; 1978 Dec 31; 30(24):1973-86. PubMed ID: 224299 [No Abstract] [Full Text] [Related]
14. [Hypoglycemia and metabolic acidosis with fructose 1-6 diphosphatase deficiency]. David M. Pediatrie; 1971 Mar 31; 26(2):223-5. PubMed ID: 4324355 [No Abstract] [Full Text] [Related]
15. Ketotic hypoglycemia and hypopituitarism. Lorentz WB. Pediatrics; 1979 Mar 31; 63(3):414-5. PubMed ID: 220586 [Abstract] [Full Text] [Related]
16. Fructose-1,6-diphosphatase deficiency in Israel. Moses SW, Bashan N, Flasterstein BF, Rachmel A, Gutman A. Isr J Med Sci; 1991 Jan 31; 27(1):1-4. PubMed ID: 1995492 [Abstract] [Full Text] [Related]
18. Biochemical observations on a case of hepatic fructose-1,6-diphosphatase deficiency. Hommes FA, Campbell R, Steinhart C, Roesel RA, Bowyer F. J Inherit Metab Dis; 1985 Jul 31; 8(4):169-73. PubMed ID: 3023747 [Abstract] [Full Text] [Related]
19. 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 31; 69(4):338-40. PubMed ID: 10870852 [Abstract] [Full Text] [Related]
20. 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 30; 55(1):41-7. PubMed ID: 4370029 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]