Literature DB >> 14760272

A six-month-old infant with liver steatosis.

Michael O Stormon1, Ernest Cutz, Katryn Furuya, Melanie Bedford, Laura Yerkes, Dean R Tolan, Annette Feigenbaum.   

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Year:  2004        PMID： 14760272      PMCID： PMC2954655          DOI： 10.1016/j.jpeds.2003.11.037

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  32 in total

1.  Activation of liver pyruvate kinase by fructose-1-phosphate.

Authors:  L V. Eggleston; H F. Woods
Journal:  FEBS Lett       Date:  1970-01-15       Impact factor: 4.124

2.  Phosphomannose isomerase deficiency: a carbohydrate-deficient glycoprotein syndrome with hepatic-intestinal presentation.

Authors:  J Jaeken; G Matthijs; J M Saudubray; C Dionisi-Vici; E Bertini; P de Lonlay; H Henri; H Carchon; E Schollen; E Van Schaftingen
Journal:  Am J Hum Genet       Date:  1998-06       Impact factor: 11.025

3.  Decrease and inhibition of liver glycogen phosphorylase after fructose. An experimental model for the study of hereditary fructose intolerance.

Authors:  J H Thurston; E M Jones; R E Hauhart
Journal:  Diabetes       Date:  1974-07       Impact factor: 9.461

4.  Depletion of liver adenosine phosphates and metabolic effects of intravenous infusion of fructose or sorbitol in man and in the rat.

Authors:  J C Bode; O Zelder; H J Rumpelt; U Wittkamp
Journal:  Eur J Clin Invest       Date:  1973-09       Impact factor: 4.686

5.  Urine uric acid to creatinine rtio--a screening test for inherited disorders of purine metabolism. Phosphoribosyltransferase (PRT) deficiency in X-linked cerebral palsy and in a variant of gout.

Authors:  J M Kaufman; M L Greene; J E Seegmiller
Journal:  J Pediatr       Date:  1968-10       Impact factor: 4.406

6.  Ultrastructural hepatocellular alterations induced by in vivo fructose infusion.

Authors:  M J Phillips; G Hetenyi; F Adachi
Journal:  Lab Invest       Date:  1970-04       Impact factor: 5.662

7.  Identification of a novel mutation (Leu 256-->Pro) in the human aldolase B gene associated with hereditary fructose intolerance.

Authors:  M Ali; G Sebastio; T M Cox
Journal:  Hum Mol Genet       Date:  1994-01       Impact factor: 6.150

8.  Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy.

Authors:  R Niehues; M Hasilik; G Alton; C Körner; M Schiebe-Sukumar; H G Koch; K P Zimmer; R Wu; E Harms; K Reiter; K von Figura; H H Freeze; H K Harms; T Marquardt
Journal:  J Clin Invest       Date:  1998-04-01       Impact factor: 14.808

9.  Features of carnitine palmitoyltransferase type I deficiency.

Authors:  S E Olpin; J Allen; J R Bonham; S Clark; P T Clayton; J Calvin; M Downing; K Ives; S Jones; N J Manning; R J Pollitt; S J Standing; M S Tanner
Journal:  J Inherit Metab Dis       Date:  2001-02       Impact factor: 4.982

10.  Liver adenine nucleotides: fructose-induced depletion and its effect on protein synthesis.

Authors:  P H Mäenpää; K O Raivio; M P Kekomäki
Journal:  Science       Date:  1968-09-20       Impact factor: 47.728
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  1 in total

1.  Increased prevalence of mutant null alleles that cause hereditary fructose intolerance in the American population.

Authors:  Erin M Coffee; Laura Yerkes; Elizabeth P Ewen; Tiffany Zee; Dean R Tolan
Journal:  J Inherit Metab Dis       Date:  2009-12-23       Impact factor: 4.982
  1 in total

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