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65. [Hereditary fructose intolerance (HFI) as cause of isolated gamma GT rise in a 5-year old boy with hepatomegaly]. Wössmann W; Wiemann J; Körber F; Gortner L Klin Padiatr; 2000; 212(3):108-9. PubMed ID: 10916780 [TBL] [Abstract][Full Text] [Related]
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68. A new aldolase B variant, N334K, is a common cause of hereditary fructose intolerance in Yugoslavia. Cross NC; Stojanov LM; Cox TM Nucleic Acids Res; 1990 Apr; 18(7):1925. PubMed ID: 2336380 [No Abstract] [Full Text] [Related]
69. Transferrin hypoglycosylation in hereditary fructose intolerance: using the clues and avoiding the pitfalls. Adamowicz M; Płoski R; Rokicki D; Morava E; Gizewska M; Mierzewska H; Pollak A; Lefeber DJ; Wevers RA; Pronicka E J Inherit Metab Dis; 2007 Jun; 30(3):407. PubMed ID: 17457694 [TBL] [Abstract][Full Text] [Related]
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72. The spectrum of aldolase B (ALDOB) mutations and the prevalence of hereditary fructose intolerance in Central Europe. Santer R; Rischewski J; von Weihe M; Niederhaus M; Schneppenheim S; Baerlocher K; Kohlschütter A; Muntau A; Posselt HG; Steinmann B; Schneppenheim R Hum Mutat; 2005 Jun; 25(6):594. PubMed ID: 15880727 [TBL] [Abstract][Full Text] [Related]
73. Mapping of a restriction fragment length polymorphism within the human aldolase B gene. Paolella G; Santamaria R; Buono P; Salvatore F Hum Genet; 1987 Oct; 77(2):115-7. PubMed ID: 2888717 [TBL] [Abstract][Full Text] [Related]
74. A possible case of transient hereditary fructose intolerance. Catto-Smith AG; Adams A J Inherit Metab Dis; 1993; 16(1):73-7. PubMed ID: 8487506 [TBL] [Abstract][Full Text] [Related]
75. Kinetic and immunological abnormalities of aldolase B in herediatry fructose intolerance. Schapira F Biochem Soc Trans; 1975; 3(2):232-4. PubMed ID: 805723 [No Abstract] [Full Text] [Related]
76. Molecular analysis of common aldolase B alleles for hereditary fructose intolerance in North Americans. Tolan DR; Brooks CC Biochem Med Metab Biol; 1992 Aug; 48(1):19-25. PubMed ID: 1524867 [TBL] [Abstract][Full Text] [Related]