[Muscle lactic dehydrogenase in myopathy: apparent persistence of the fetal type].
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Disease↗
Biomedical subjects
F SCHAPIRA
Publications and source records attributed to F SCHAPIRA.
[Preliminary note on the clinical, biological, histochemical and enzymatic study of essential familial fructosuria].
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Body Fluids↗
[The length of stay in the plasma of aldolase in the rabbit: study aided by aldolase labelled with radioactive iodine].
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Animals↗
[Fructose-1-phospho-aldolase of the serum].
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Fructose↗
[Hyperaldolasemia, a biological sign of primary cancer of the liver].
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Fructose-Bisphosphate Aldolase↗
[Aldolase activity & age of erythrocytes].
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Aldehyde-Lyases↗
Serum enzymes in the physiopathology of muscle.
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Enzymes↗
[Distribution and activity of 1-phosphofructoaldolase].
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Lyases↗
Genetics of haemochromatosis.
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Hemochromatosis↗
[Blood aldolases & transaminases during glycogen storage disease].
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Aldehyde-Lyases↗
[Presence of two aldolases of different types in blood].
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Aldehyde-Lyases↗
[Aldolase excess in blood in myopathic mice].
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Animals↗
Factors of hyperaldolasemia during myopathies.
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Disease↗
Hyperaldolasemia caused by glycyrrhinic acid.
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Flavoring Agents↗
[Hyperaldolasemia and hypertransaminasemia caused by desoxycorticosterone].
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Desoxycorticosterone↗
Biochemical study of muscle in progressive muscular dystrophy.
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Humans↗
[Calcemia; technical errors and interpretations to avoid; methods with complexes].
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Blood↗
[Elevation of the serum aldolase level; biochemical test in myopathy].
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Fructose-Bisphosphate Aldolase↗