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Deficiency of fructokinase

Known as: Hepatic fructokinase deficiency, FRUCTOSURIA, ESSENTIAL, Ketohexokinase deficiency 
National Institutes of Health

Related topics

Related topics

7 relations
Autosomal recessive inheritanceFructose-1,6-Diphosphatase DeficiencyHereditary fructose intolerance syndromeKHK gene

Broader (1)

Fructokinases

Papers overview

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2020
2020
[ESSENTIAL FRUCTOSURIA].
Review
2007
Review
2007
Doctor, my son is so tired... about a case of hereditary fructose intolerance.
Highly Cited
1983
Highly Cited
1983
Essential fructosuria, hereditary fructose intolerance, and fructose-1,6-diphosphatase deficiency
1976
1976
3Disorders of fructose metabolism
1968
1968
Über die Verwertung und renale Ausscheidung von Fructose während ihrer langdauernden intravenösen Zufuhr
Zusammenfassung1. Vor der enzymatischen Bestimmung von Fructose wird Glucose mittels Glucoseoxydase zerstört, falls die zur… 
1966
1966
Black-copper reduction reaction simulating alkaptonuria. Occurrence after intravenous urography.
CERTAIN inborn errors of carbohydrate metabolism, including galactosuria, lactosuria and fructosuria, certain drugs, alkaptohuria… 
Review
1948
Review
1948
Essential fructosuria in two siblings.
ESSENTIAL fructosuria, apparently a harmless condition, is an extremely rare error of metabolism, the recognition of which is of… 
1947
1947
The diagnosis of the less common meliturias; including pentosuria and fructosuria.
1942
1942
ESSENTIAL FRUCTOSURIA: ITS PATHOPHYSIOLOGY
In 1876 Zumier 1 and Czapek 2 each reported the occurrence of fructose in the urine of a nondiabetic patient. Though it is clear… 
1934
1934
Essential fructosuria. Report of three cases with metabolic studies.
Fructosuria, otherwise termed "levulosuria," was recognized soon after polarization of urines for the detection of sugar became… 
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