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D-GLYCERIC ACIDURIA
An autosomal recessive genetic disorder caused by mutations in the GLYCTK gene, encoding glycerate kinase. The condition is characterized by…
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National Institutes of Health
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Related topics
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11 relations
Autosomal recessive inheritance
Cerebral atrophy
Encephalopathies
Failure to Thrive
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
1993
1993
A new case of hyperoxaluria type II
L. Vilarinho
,
R. Araujo
,
+5 authors
D. Rabier
Journal of Inherited Metabolic Disease
1993
Corpus ID: 31442058
Hyperoxaluria type II (McKusick 260000) is a very rare metabolic disorder characterized by renal disease and excessive excretion…
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1988
1988
Primary hyperoxaluria andl-glyceric aciduria in the cat
W. Blakemore
,
M. Heath
,
M. Bennett
,
C. Cromby
,
R. Pollitt
Journal of Inherited Metabolic Disease
1988
Corpus ID: 29292698
L-Glyceric aciduria (primary hyperoxaluria type 2; McKusick 26000) is a rare inherited disorder characterized in man by recurrent…
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Review
1988
Review
1988
Primary Hyperoxaiuria in Children
T. Barratt
,
V. Sperling
,
G. A. Rose
,
R. Trompeter
1988
Corpus ID: 74854187
Primary hyperoxaluria is an uncommon autosomal recessive disorder. The clinical features consist of nephrocalcinosis, recurrent…
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1984
1984
In vivo studies on the metabolic derangement in a patient with D-glyceric acidaemia and hyperglycinaemia
S. Kolvraa
,
N. Gregersen
,
E. Christensen
Journal of Inherited Metabolic Disease
1984
Corpus ID: 2488913
In a mentally retarded boy, who excreted elevated amounts of glycine,d-glyceric acid and acylglycines and whose cells exhibited…
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1978
1978
The synthesis of oxylate from hydroxypyruvate by isolated perfused rat liver. The mechanism of hyperoxaluria in L-glyceric aciduria.
L. L. Liao
,
K. E. Richardson
Biochimica et Biophysica Acta
1978
Corpus ID: 29961319
Hydroxypyruvate and glycolate inhibited the oxidation of [U-14C]glyoxylate to [14C]oxalate in isolated perfused rat liver, but…
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1977
1977
D-Glyceric-Acidaemia in Non-Ketotic Hyperglycinaemia: A New Inborn Error of Metabolism
N. Brandt
,
E. Christensen
,
S. Kolvraa
,
K. Rasmussen
Annals of Clinical Biochemistry
1977
Corpus ID: 5863738
The patient, a boy, was born of healthy parents after a normal pregnancy. Birth was uncomplicated; birth weight 3350 g. In the…
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1966
1966
Use of vinyl magnesium bromide in the synthesis of labeled compounds: new preparations of glycerol-1-C14 and glyceric acid-1-C14.
L. Pichat
,
M. Herbert
,
F. Aubert
Advances in tracer methodology
1966
Corpus ID: 33098492
The biological importance of glycerol and glyceric acid is well known; as a consequence, it is very useful to have methods for…
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1964
1964
D-5-1 Synthesis of ^ C Labelled Compounds for Radioisotope Studies of Fatty Acid Metabolism : Glycerol-1-^ C, Glyceric Acid-1-^ C, Palmitic Acid-16-^ C, Stearic Acid-18-^ C, Caprylic Acid-8-^ C(Amino…
L. Pichat
,
M. Herbert
,
J. Guermont
,
F. Aubert
1964
Corpus ID: 82545850
1962
1962
The stereochemistry of the reaction catalyzed by D-glyceric 3-dehydrogenase.
G. Krakow
,
S. Udaka
,
B. Vennesland
Biochemistry
1962
Corpus ID: 27308851
1937
1937
Specific Action of Ferricyanide on Ærobic Glycolysis of Tumour Cells
B. Mendel
,
F. Strelitz
Nature
1937
Corpus ID: 4111067
IT has been found1 that ferricyanide (10−2 mol./litre) stops œrobic glycolysis of mammalian tumour cells, but it does not affect…
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