THE THALASSAEMIA SYNDROMES. 3. A SEVERE FORM OF THALASSAEMIA MINOR WITH SLIGHTLY ELEVATED FETAL HAEMOGLOBIN. STUDY OF TWO FAMILIES.
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Fetal Hemoglobin↗
Biomedical subjects
M AKSOY
Publications and source records attributed to M AKSOY.
FETAL HAEMOGLOBIN IN ACQUIRED APLASTIC ANAEMIA.
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Anemia↗
[HEPATOCEREBRAL OR HEPATOLENTICULAR DEGENERATION].
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Adolescent↗
[STATE OF LOW IRON LEVEL IN CASES OF CONGENITAL HEMOLYTIC ANEMIA, SUCH AS SICKLE CELL ANEMIA AND THALASSEMIA].
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Anemia↗
[MODE OF ACTION OF CHELATOR AGENTS IN THE TREATMENT OF HEPATOLENTICULAR DEGENERATION].
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Chelating Agents↗
Thalassemiahemoglobin E disease in Turkey, with hypersplenism in one case.
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Anemia↗
"Cystography" in a case of pancreatic pseudocyst.
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Fluoroscopy↗
THE COMBINATION OF HEREDITARY ELLIPTOCYTOSIS WITH HETEROZYGOUS BETA-THALASSAEMIA. STUDY OF A TURKISH FAMILY.
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Anemia↗
[HOMOZYGOUS HEMOGLOBIN S AND ALPHA THALASSEMIC DISEASE].
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Anemia↗
[TYPES OF SICKLE CELL- THALASSEMIC DISEASES. A. SICKLE CELL-BETA THALASSEMIA. B. SICKLE CELL-ALPHA THALASSEMIA. STUDY OF 6 CASES IN 5 FAMILIES].
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Anemia↗
THE FIRST OBSERVATION OF HOMOZYGOUS HEMOGLOBIN S-ALPHA THALASSEMIA DISEASE AND TWO TYPES OF SICKLE CELL THALASSEMIA DISEASE: (A) SICKLE CELL-ALPHA THALASSEMIA DISEASE, (B) SICKLE CELL-BETA THALASSEMIA DISEASE.
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Anemia↗
[THE COMBINATION OF HEREDITARY ELLIPTOCYTOSIS AND HETEROZYGOUS BETA THALASSEMIA. (INVESTIGATION OF A TURKISH FAMILY)].
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Anemia↗
[STUDIES ON CARBOHYDRATE METABOLISM IN PATIENTS WITH IRON DEFICIENCY ANEMIA OF LONG DURATION].
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Anemia↗
Haemoglobins S and E in Turkish people.
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Ethnology↗
Hereditary elliptocytosis. Study of a Turkish family.
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Elliptocytosis, Hereditary↗
[Thalassemia-hemoglobin E disease and hypersplenism].
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Anemia↗
[Hemoglobin S and E in Turkey].
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Hemoglobin, Sickle↗
[Acute recurrent neutropenia].
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Agranulocytosis↗