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Journal Articles

Hereditary Hemolytic Anemia Associated With Abnormal Membrane Lipid. II. Ion Permeability and Transport Abnormalities

Stephen B. Shohet, M.D., David G. Nathan, M.D., Barbara M. Livermore, Stephen A. Feig, Ernst R. Jaffé, M.D.

Blood (1973) 42 (1): 1–8.

https://doi.org/10.1182/blood.V42.1.1.1

Published: 1973

Journal Articles

Studies on Human Erythrocyte Nucleotide Metabolism. II. Nonspherocytic Hemolytic Anemia, High Red Cell ATP, and Ribosephosphate Pyrophosphokinase (RPK, E.C. 2.7.6.1) Deficiency

William N. Valentine, M.D., Helen M. Anderson, M.D., Donald E. Paglia, M.D., Ernst R. Jaffé, M.D., Patricia N. Konrad, M.D., Susan R. Harris, M.D., Klaus K. Kürschner

Blood (1972) 39 (5): 674–684.

https://doi.org/10.1182/blood.V39.5.674.674

Published: 1972

Journal Articles

G6PD Deficiency and Chronic Hemolysis: Four New Mutants—Relationships Between Clinical Syndrome and Enzyme Kinetics

MARIO C. RATTAZZI, M.D., LAURENCE M. CORASH, M.D., GEORGE E. VAN ZANEN, M.D., ERNST R. JAFFÉ, M.D., SERGIO PIOMELLI, M.D.

Blood (1971) 38 (2): 205–218.

https://doi.org/10.1182/blood.V38.2.205.205

Published: 1971

Journal Articles

Reduction of Oxidized Glutathione in Normal and Glucose-6-Phosphate Dehydrogenase Deficient Erythrocytes and Their Hemolysates

EGMOND E. RIEBER, M.D., ERNST R. JAFFÉ, M.D.

Blood (1970) 35 (2): 166–172.

https://doi.org/10.1182/blood.V35.2.166.166

Published: 1970

Journal Articles

Clinical Profile: Hereditary Hemolytic Disorders and Enzymatic Deficiencies of Human Erythrocytes

ERNST R. JAFFÉ

Blood (1970) 35 (1): 116–134.

https://doi.org/10.1182/blood.V35.1.116.116

Published: 1970

Journal Articles

The Reduction of Methemoglobin in Erythrocytes of a Patient with Congenital Methemoglobinemia, Subjects with Erythrocyte Glucose-6-Phosphate Dehydrogenase Deficiency, and Normal Individuals

ERNST R. JAFFÉ, M.D.

Blood (1963) 21 (5): 561–572.

https://doi.org/10.1182/blood.V21.5.561.561

Published: 1963

NARROW

Hereditary Hemolytic Anemia Associated With Abnormal Membrane Lipid. II. Ion Permeability and Transport Abnormalities

Studies on Human Erythrocyte Nucleotide Metabolism. II. Nonspherocytic Hemolytic Anemia, High Red Cell ATP, and Ribosephosphate Pyrophosphokinase (RPK, E.C. 2.7.6.1) Deficiency

G6PD Deficiency and Chronic Hemolysis: Four New Mutants—Relationships Between Clinical Syndrome and Enzyme Kinetics

Reduction of Oxidized Glutathione in Normal and Glucose-6-Phosphate Dehydrogenase Deficient Erythrocytes and Their Hemolysates

Clinical Profile: Hereditary Hemolytic Disorders and Enzymatic Deficiencies of Human Erythrocytes

The Reduction of Methemoglobin in Erythrocytes of a Patient with Congenital Methemoglobinemia, Subjects with Erythrocyte Glucose-6-Phosphate Dehydrogenase Deficiency, and Normal Individuals

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ASH Publications

American Society of Hematology

Hereditary Hemolytic Anemia Associated With Abnormal Membrane Lipid. II. Ion Permeability and Transport Abnormalities

Studies on Human Erythrocyte Nucleotide Metabolism. II. Nonspherocytic Hemolytic Anemia, High Red Cell ATP, and Ribosephosphate Pyrophosphokinase (RPK, E.C. 2.7.6.1) Deficiency

G6PD Deficiency and Chronic Hemolysis: Four New Mutants—Relationships Between Clinical Syndrome and Enzyme Kinetics

Reduction of Oxidized Glutathione in Normal and Glucose-6-Phosphate Dehydrogenase Deficient Erythrocytes and Their Hemolysates

Clinical Profile: Hereditary Hemolytic Disorders and Enzymatic Deficiencies of Human Erythrocytes

The Reduction of Methemoglobin in Erythrocytes of a Patient with Congenital Methemoglobinemia, Subjects with Erythrocyte Glucose-6-Phosphate Dehydrogenase Deficiency, and Normal Individuals

Email alerts

ASH Publications

American Society of Hematology

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