The use of leucocytes as an aid in the diagnosis of glycogen storage disease type II (Pompe's disease).
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Antibodies↗
Biomedical subjects
J F Koster
Publications and source records attributed to J F Koster.
Hepatic phosphorylase deficiency. Its differentiation from other hepatic glycogenoses.
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Administration, Oral↗
On the molecular basis of pyruvate kinase deficiency. I. Primary defect or conseqence of increased glutathione disulfide concentration.
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Adult↗
Some kinetic properties of the allosteric M-type pyruvate kinase from rat liver; influence of pH and the nature of amino acid inhibition.
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Adenosine Triphosphate↗
Hepatic phosphorylase deficiency: a biochemical study.
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Adenosine Monophosphate↗
Two interconvertible forms of L-type pyruvate kinase from rat liver.
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Allosteric Regulation↗
M-type pyruvate kinase of leucocytes: an allosteric enzyme.
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Allosteric Regulation↗
Distribution of L- and M-type pyruvate kinase between parenchymal and Kupffer cells of rat liver.
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Animals↗
Human erythrocyte phosphofructokinase: its purification and some properties.
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Adenosine Triphosphate↗
Influence of 2,3-diphosphoglycerate on phosphofructokinase of human erythrocytes?
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Adenosine Diphosphate↗
The influence of glucose I,6-diphosphate on the enzymatic activity of pyruvate kinase.
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Adenosine Triphosphate↗
A new variant of red blood cell pyruvate kinase deficiency.
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Allosteric Regulation↗
Pyruvate kinase in cultivated amniotic fluid cells.
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Amniotic Fluid↗
The electrophoretic pattern and activities of acid and neutral maltase of cultivated fibroblasts and amniotic fluid cells from controls and patients with the variant of glycogen storage disease type II (Pompe's disease).
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Amniotic Fluid↗
The use of leucocytes as an aid in the diagnosis of a variant of glycogen storage disease type II (Pompe's disease).
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Cardiomegaly↗
The effect of urea and temperature on red blood cell pyruvate kinase.
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Chemical Phenomena↗
Human erythrocyte pyruvate kinase. Its purification and some properties.
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Adenine Nucleotides↗
Choice of leucocyte preparation in the diagnosis of glycogen storage disease type II (Pompe's disease).
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Cardiomegaly↗