Thalassemia-hemoglobin C disease; a new syndrome presumably due to the combination of the genes for thalassemia and hemoglobin C.
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Anemia↗
Biomedical subjects
E KAPLAN
Publications and source records attributed to E KAPLAN.
A system of nomenclature for the varieties of human hemoglobin.
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Hemoglobins↗
Further studies on hemoglobin C. I. A description of three additional families segregating for hemoglobin C and sickle cell hemoglobin.
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Anemia↗
Further studies on hemoglobin C. II. The hematologic effects of hemoglobin C alone and in combination with sickle cell hemoglobin.
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Anemia↗
The significance of visible iron in red cell precursors.
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Bone Marrow↗
Studies concerning a new inherited abnormality of hemoglobin.
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Hemoglobins↗
Lead poisoning in young children.
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Child↗
A new inherited abnormality of hemoglobin and its interaction with sickle cell hemoglobin.
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Anemia↗
The Q-T interval in the electrocardiogram of children with tuberculosis.
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Electrocardiography↗
Erythrocyte survival studies in childhood. I. Methods and general observations.
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Erythrocyte Aging↗
Erythrocyte survival studies in childhood. II. Studies in Mediterranean anemia.
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Anemia↗
Erythrocyte survival studies in childhood. III. Unusual familial hemolytic anemias associated with intrinsic erythrocyte abnormality.
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Anemia↗
Familial nonspherocytic hemolytic anemia.
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Anemia↗
Relation of thiols to heavy metal inhibition.
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Metals, Heavy↗
Effects of inhibitor combinations on membrane potentials of the synovialis.
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Humans↗
Robert Recorde and the authorities of uroscopy.
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Diagnosis↗