[Aldolase excess in blood in myopathic mice].
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Animals↗
Biomedical subjects
F SCHAPIRA
Publications and source records attributed to F SCHAPIRA.
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↗
[Incorporation of radionitrogen-labeled glycine into myosin; role of muscle atrophy and topography].
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Atrophy↗
[Enzyme activity in human muscles; research on comparative biochemistry in normal and myopathic men, and in rats].
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Animals↗
[Rapid micro determination of serum calcium].
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Blood↗
[Muscle enzymes in experimental and human pathology].
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Enzymes↗
[Studies on the biochemical aspects of human muscle diseases].
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Disease↗
[Adaptive enzymes in higher animals].
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Animals↗
[Serum lactic dehydrogenase from mothers of children with muscular dystrophy].
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Child↗
[The enzymatic defect of benign fructosuria].
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Fructokinases↗
[Rapid method of determining the iron-saturation capacity of transferrin in the serum].
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Hematologic Tests↗
[Biological anomalies in the apparently healthy transmitters of muscular dystrophy].
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Clinical Enzyme Tests↗
[DETERMINATION OF SERUM CREATINE KINASE].
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Adenosine Triphosphate↗