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Pentosuria

Known as: L-XYLULOSE REDUCTASE DEFICIENCY, L-XYLULOSURIA, Xylulosuria 
National Institutes of Health

Papers overview

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Review
2015
Review
2015
Dicarbonyl/l‐xylulose reductase (DCXR; SDR20C1), a member of the short‐chain dehydrogenase/reductase (SDR) superfamily catalyzes… 
Review
2008
Review
2008
SummaryGarrod presented his concept of ‘the inborn error of metabolism’ in the 1908 Croonian Lectures to the Royal College of… 
1985
1985
Essential pentosuria is the result of a partial deficiency of l-xylulose reductase. Red blood cells of normal individuals have… 
1970
1970
Abstract The enzyme defect in pentosuria has been assumed to be NADP-linked xylitol dehydrogenase, a specific enzyme found in… 
1961
1961
Endogenous serum l-xylulose concentration exceeds 1 mg. per 100 ml. in pontosuric patients, and the level rises several-fold… 
Review
1960
Review
1960
Dicusson Hemiatrophy of the body is usually facial, and not always progressive and unilateral. Like other hereditary… 
1959
1959
ESSENTIAL pentosuria is a rare, recessive genetic metabolic disorder characterized by the excretion of gram quantities of L… 
1956
1956
2. CHROMATOGRAPHIC STUDIES Examinations by paper chromatography were carried out on 43 specimens of 24-hour urine from 21…