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[FACTOR MAP OUTLINE OF THE X CHROMOSOME].
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HEREDITARY AND ACQUIRED BLOOD FACTORS IN THE NEGROID POPULATION OF SURINAM. II. THE INCIDENCE OF HAEMOGLOBIN ANOMALIES AND THE DEFICIENCY OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE.
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THE SEPARATION OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE-DEFICIENT ERYTHROCYTES FROM THE BLOOD OF HETEROZYGOTES FOR GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY.
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MORPHOLOGICAL DEMONSTRATION OF 2 RED CELL POPULATIONS IN HUMAN FEMALES HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY.
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GLUCOSE-6-PHOSPHATE DEHYDROGENASE, COLOUR VISION AND XG BLOOD GROUPS IN GREECE: LINKAGE AND POPULATION DATA.
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GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND FALCIPARUM MALARIA.
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[GENETIC STUDY OF THE GLYCOGENOSES].
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[NORMAL AND PATHOLOGICAL METABOLISM OF RED CELLS].
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[HEMOGLOBIN, METHEMALBUMIN AND HAPTOGLOBINEMIA IN PLASMA OF NEWBORNS WITH HEMOLYTIC JAUNDICE DUE TO ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY. ELECTROPHORETIC RESEARCH].
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[METABOLIC ANOMALIES OF THE BLOOD CELLS AS A CAUSE OF DISEASE].
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[DREPANOCYTEMIA, ERYTHROCYTIC GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY (G-6-PD) AND MALARIA IN THE CUANGO POST (LUNDA-ANGOLA)].
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[THE CLINICAL SIGNIFICANCE OF HEREDITARY GLUCOSE-6-PHOSPHATE-DEHYDROGENASE INACTIVITY].
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ROLE OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN ACUTE HEMOLYTIC CRISIS AND NEONATAL JAUNDICE.
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[ENZYMOPRIVIC HEMOLYTIC ANEMIA].
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[HEMOLYTIC ANEMIA CAUSED BY ENZYMATIC DEFECT (GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY). RESEARCH IN CHILEAN POPULATIONS: MAPUCHE, PASCUENSE AND ALACALUFE].
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[BEHAVIOR OF OXYGEN CONSUMPTION AND ANAEROBIC GLYCOLYSIS IN ERYTHROCYTES OF PATIENTS SUBJECTED TO SPLENECTOMY FOR IMMUNOLOGIC HEMOLYTIC ANEMIA].
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