Deficiency of fructokinase

Known as: Hepatic fructokinase deficiency, FRUCTOSURIA, ESSENTIAL, Ketohexokinase deficiency 
 

Topic mentions per year

Topic mentions per year

1946-2017
02419462016

Papers overview

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2015
2015
Elevated blood fructose concentrations constitute the basis for organ dysfunction in fructose-induced metabolic syndrome. We… (More)
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2003
2003
Alternative splicing of the ketohexokinase (fructokinase) gene generates a "central" predominantly hepatic isoform… (More)
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2001
2001
Ketohexokinase (KHK; E.C. 2.7.1.3) catalyses the (reversible) phosphorylation of fructose to fructose-1-phosphate. KHK is the… (More)
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1994
1994
Essential fructosuria is one of the oldest known inborn errors of metabolism. It is a benign condition which is believed to… (More)
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1992
1992
Erythrocytes of 3 adult siblings with essential fructosuria contained 45-200 mumol/l fructose 3-phosphate (Fru-3-P), i.e. 3-15… (More)
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1987
1987
Apart from classical X-linked ornithine transcarbamylase (OTC) deficiency (McKusick 31125), several clinically and biochemically… (More)
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1981
1981
Hereditary fructose intolerance (HFI) is a potentially life-threatening disorder and can be suspected from a detailed nutritional… (More)
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1969
1969
 
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1965
1965
 
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1947
1947
 
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