HAEMOGLOBIN NICOSIA. AN ALPHA-CHAIN VARIANT AND ITS COMBINATION WITH BETA-THALASSAEMIA.
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Buffers↗
Biomedical subjects
P FESSAS
Publications and source records attributed to P FESSAS.
THE DISTRIBUTION OF HEMOGLOBIN TYPES IN THALASSEMIC ERYTHROCYTES.
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Blood Protein Electrophoresis↗
ABSORPTION SPECTRA OF INCLUSION BODIES IN BETA-THALASSEMIA.
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Centrifugation↗
THALASSEMIAS, ABNORMAL HEMOGLOBINS AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN THE ARTA AREA OF GREECE: DIAGNOSTIC AND GENETIC ASPECTS OF COMPLETE VILLAGE STUDIES.
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Environment↗
THALASSAEMIA, GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY, SICKLING, AND MALARIAL ENDEMICITY IN GREECE: A STUDY OF FIVE AREAS.
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Adolescent↗
ALPHA-CHAIN OF HUMAN HEMOGLOBIN: OCCURRENCE IN VIVO.
A minor hemoglobin component, apparently representing uncombined alpha-chains has been detected in the hemolysates of persons with inherited beta-chain deficiency of moderate or severe degree. This finding supports the hypothesis that there is independent control of the synthesis of alpha-chains.
Blood Protein Electrophoresis↗
HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN IN GREECE. A STUDY AND A COMPARISON.
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Black People↗
Serum-cholesterol and thalassemia trait.
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Anemia↗
Three inherited red-cell abnormalities in a district of Greece. Thalassaemia, sickling, and glucose-6-phosphate-dehydrogenase deficiency.
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Anemia↗
ACUTE HEMOLYSIS DUE TO NAPHTHALENE INHALATION.
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Erythrocytes↗
The normal minor components of human foetal haemoglobin.
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Fetal Hemoglobin↗
Inclusions of hemoglobin erythroblasts and erythrocytes of thalassemia.
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Erythroblasts↗
OBSERVATIONS ON HEMOGLOBIN "PYLOS": THE HEMOGLOBIN PYLOS-HEMOGLOBIN S COMBINATION.
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Greece↗
Neonatal jaundice in glucose-6-phosphate-dehydrogenase-deficient infants.
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Glucose-6-Phosphate↗
Absence of haemoglobin A2 in an adult.
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Hemoglobin A2↗
Two-dimensional paper-agar electrophoresis of haemoglobin.
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Agar↗
Types of thalassaemia-trait carriers as revealed by a study of their incidence in Greece.
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Anemia↗