A. S. Schneider

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Triosephosphate isomerase de ® ciency : historical perspectives and molecular aspects

A. S. Schneider, 2022 .

Sensitive fluorometry of heat-stable alkaline phosphatase (Regan enzyme) activity in serum from smokers and nonsmokers.

A. S. Schneider, H. Muensch, W. Maslow, 1983, Clinical chemistry.

Hereditary hemolytic anemia with triosephosphate isomerase deficiency: Studies in kindreds with coexistent sickle cell trait and erythrocyte glucose-6-phosphate dehydrogenase deficiency

W. Valentine, D. Paglia, A. S. Schneider, 1966 .

Optimization of reactant concentrations for maximizing sensitivities of competitive immunoassays

C. J. Halfman, A. S. Schneider, 1981 .

ERYTHROCYTE CARBOHYDRATE METABOLISM IN HEREDITARY SPHEROCYTOSIS.

E. L. Coe, K. Ibsen, A. S. Schneider, 1963, The Journal of clinical investigation.

Screening for homozygous and heterozygous alpha 1-antitrypsin deficiency. Protein electrophoresis on cellulose acetate membranes.

A. S. Schneider, J. Lieberman, C. Mittman, 1969, JAMA.

HEREDITARY HEMOLYTIC ANEMIA WITH TRIOSEPHOSPHATE ISOMERASE DEFICIENCY.

W. Valentine, A S SCHNEIDER, W N VALENTINE, 1965, The New England journal of medicine.

The effect of dodecyl sulfate on immunoglobulin hapten binding.

C. J. Halfman, A. S. Schneider, R. Dowe, 1986, Molecular immunology.

Triosephosphate isomerase deficiency: historical perspectives and molecular aspects.

A. S. Schneider, 2000, Bailliere's best practice & research. Clinical haematology.

Hereditary hemolytic anemia with hexokinase deficiency. Role of hexokinase in erythrocyte aging.

F. Oski, W. Valentine, D. Paglia, 1967, The New England journal of medicine.

STUDIES ON CHROMATED ERYTHROCYTES. EFFECT OF SODIUM CHROMATE ON ERYTHROCYTE GLUTATHIONE REDUCTASE.

W. Valentine, A. S. Schneider, F. G. Ebaugh, 1964, The Journal of clinical investigation.

Studies on Chromated Erythrocytes. MECHANISMS OF CHROMATE INHIBITION OF GLUTATHIONE REDUCTASE

W. Valentine, A. S. Schneider, G. Koutras, 1965, British journal of haematology.

An unusual hematological syndrome with pyruvate-kinase deficiency and thalassemia minor in the kindreds.

W. Valentine, D. Paglia, A. S. Schneider, 1968, Acta haematologica.

Triose phosphate isomerase deficiency in 3 French families: two novel null alleles, a frameshift mutation (TPI Alfortville) and an alteration in the initiation codon (TPI Paris).

M. Mayer, D. Heron, C. Valentin, 2000, Blood.

Hereditary Nonspherocytic Hemolytic Anemia with Pyruvate Kinase Deficiency.

A. S. Schneider, K. Tanaka, W. N. Valentine, 1963 .

Direct measurement of fluorescence polarization or anisotropy

C. J. Halfman, A. S. Schneider, 1982 .