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Galactosuria
Known as:
Increased urinary galactose level
Elevated concentration of galactose in the urine. [HPO:probinson]
National Institutes of Health
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Related topics
Related topics
3 relations
Classical galactosemia
Deficiency of galactokinase
UDPglucose 4-epimerase deficiency disease
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
An intravenous galactose tolerance test and its use in hepatobiliary diseases.
B. Tengström
Acta Medica Scandinavica
2009
Corpus ID: 28287776
The paper describes an intravenous galactose tolerance test performed by a single injection of 350 mg of galactose per kg body…
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2003
2003
Capillary electrophoresis with laser-induced fluorescence detection for laboratory diagnosis of galactosemia.
C. J. Easley
,
L. Jin
,
K. B. Prestø Elgstøen
,
E. Jellum
,
J. Landers
,
J. Ferrance
Journal of Chromatography A
2003
Corpus ID: 23467333
1999
1999
Homogeneous bioluminescence assay for galactosuria: interference and kinetic analysis.
J. Eu
,
C. Wang
,
J. Andrade
Analytical Biochemistry
1999
Corpus ID: 44898806
Elevated galactose concentration in urine is an important clinical symptom of galactosemia and other metabolic disorders. A…
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Highly Cited
1994
Highly Cited
1994
Blood sugar levels and renal sugar excretion after the intake of high carbohydrate diets in cats.
E. Kienzle
Journal of NutriLife
1994
Corpus ID: 11607163
The effect of starch and sugars on blood sugar level and renal excretion of sugars and galactitol was investigated. Fifty-nine…
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Review
1979
Review
1979
Review of Metabolic Screening Program of Children's Hospital, Vancouver, British Columbia. 1971--1977.
L. Wong
,
D. Hardwick
,
D. Applegarth
,
A. Davidson
Clinical Biochemistry
1979
Corpus ID: 43747665
1971
1971
Hereditary galactokinase deficiency
J. Cook
,
N. Don
,
T. Mann
Archives of Disease in Childhood
1971
Corpus ID: 10588376
A baby with galactokinase deficiency, a recessive inborn error of galactose metabolism, is described. The case is exceptional in…
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Highly Cited
1968
Highly Cited
1968
Hypergalactosemia and galactosuria due to galactokinase deficiency in a newborn.
O. Thalhammer
,
R. Gitzelmann
,
M. Pantlitschko
Pediatrics
1968
Corpus ID: 42383242
The detection in a screening program of a newborn infant with galactokinase deficiency is reported. Hypergalactosemia…
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1961
1961
Mellituria, a paper chromatographic study.
H. Bickel
Jornal de Pediatria
1961
Corpus ID: 28105273
1960
1960
Cutaneous findings in phenylketonuria.
T. Fleisher
,
I. Zeligman
Archives of Dermatology
1960
Corpus ID: 45597600
Phenylpyruvic oligophrenia is a heritable disorder characterized by mental retardation and the excretion of large amounts of…
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Review
1950
Review
1950
Galactose diabetes (galactosemia)
L. S. Bell
,
W. C. Blair
,
S. Lindsay
,
S. J. Watson
1950
Corpus ID: 71407883
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