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MeSH Review

Fructose-1,6-Diphosphatase Deficiency

 
 
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Disease relevance of Fructose-1,6-Diphosphatase Deficiency

 

High impact information on Fructose-1,6-Diphosphatase Deficiency

 

Chemical compound and disease context of Fructose-1,6-Diphosphatase Deficiency

References

  1. Triosidines: novel Maillard reaction products and cross-links from the reaction of triose sugars with lysine and arginine residues. Tessier, F.J., Monnier, V.M., Sayre, L.M., Kornfield, J.A. Biochem. J. (2003) [Pubmed]
  2. Inborn errors of fructose metabolism. Hommes, F.A. Am. J. Clin. Nutr. (1993) [Pubmed]
  3. Deficiency of glucose-6-phosphate dehydrogenase found in a case of hepatic fructose-1,6-diphosphatase deficiency. Kinugasa, A., Kusunoki, T., Iwashima, A. Pediatr. Res. (1979) [Pubmed]
  4. Detection of heterozygotes for fructose-1,6-diphosphatase deficiency by measuring fructose-1,6-diphosphatase activity in monocytes cultured with calcitriol. Kikawa, Y., Takano, T., Nakai, A., Shigematsu, Y., Sudo, M. Clin. Chim. Acta (1993) [Pubmed]
  5. Fructose and glucagon loading in siblings with fructose-1,6-diphosphatase deficiency in fed state. Nagai, T., Yokoyama, T., Hasegawa, T., Tsuchiya, Y., Matsuo, N. J. Inherit. Metab. Dis. (1992) [Pubmed]
  6. Inherited disorders of carbohydrate metabolism in children studied by 13C-labelled precursors, NMR and GC-MS. Lapidot, A. J. Inherit. Metab. Dis. (1990) [Pubmed]
  7. Hepatic metabolites and uric acid excretion in fructose-1,6-diphosphatase deficiency. Velázquez, A., DeCéspedes, C., DeVivo, D.C., Costin, G., Shaw, K.N. J. Inherit. Metab. Dis. (1988) [Pubmed]
  8. Glycerol-3-phosphate excretion in fructose-1,6-diphosphatase deficiency. Krywawych, S., Katz, G., Lawson, A.M., Wyatt, S., Brenton, D.P. J. Inherit. Metab. Dis. (1986) [Pubmed]
  9. Fructose-1,6-diphosphatase deficiency: glycerol excretion during fasting test. Dremsek, P.A., Sacher, M., Stögmann, W., Gitzelmann, R., Bachmann, C. Eur. J. Pediatr. (1985) [Pubmed]
 
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