Osseous changes in Wilson's disease. A radiologic study of nine patients.
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Adolescent↗
Biomedical subjects
M Aksoy
Publications and source records attributed to M Aksoy.
Hemoglobin Istanbul: substitution of glutamine for histidine in a proximal histidine (F8(92) ).
A presumably spontaneous mutation has resulted in the formation of Hemoglobin (Hb) Istanbul in which glutamine is substituted for histidine in the proximal position of the beta-chain (F8(92)). The anemia and other physiological effects that occur in the presence of Hb Istanbul were much ameliorated by splenectomy. Hb Istanbul is a relatively unstable molecule which produces a rather moderate case of "unstable hemoglobin hemolytic anemia."In the determination of structure, a method of preferential cleavage of an aspartyl-proline bond at residues 99-100 of the beta-chain was used.
Adult↗
Haematological effects of chronic benzene poisoning in 217 workers.
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Adolescent↗
On the pathogenesis of the hepatosplenomegaly in chronic iron deficiency anemia. A study in eleven patients.
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Adolescent↗
Thalassaemia intermedia: a genetic study in 11 patients.
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Adolescent↗
"Porcelain gallbladder" in a case of thalassemia intermedia.
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Adult↗
The presence of a haemolytic component and the type of hypochromic microcytic anaemia in kala-azar.
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Anemia, Hypochromic↗
Some problems of hemoglobin patterns in different thalassemic syndromes showing the heterogeneity of beta-thalassemia genes.
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Adult↗
Megaloblastic anemia in the course of vinblastine sulphate (VELBE) therapy.
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Adolescent↗
On the platelet levels in chronic iron deficiency anemia.
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Anemia, Hypochromic↗
Aplastic anaemia after propylthiouracil.
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Adult↗
Iron-sorbital complex as a possible factor in the development of a blastic crisis in chronic myeloid leukemia.
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Adult↗
Combination of hereditary elliptocytosis and heterozygous beta-thalassaemia: a family study.
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Adult↗
Haemoglobin H disease study of an Eti-Turk family.
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Adolescent↗
The combination of hereditary spherocytosis and heterozygous beta-thalassaemia. A family study.
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Adult↗
[Determination of G. 6PD and other enzymes, abnormal and fetal hemoglobins, free alfa and beta chains and haptoglobins in cord blood in thalassemic groups. I].
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Blood Group Antigens↗
[Determination of G. 6PD and other enzymes, abnormal and fetal hemoglobins, free alfa and beta chains and haptoglobins in cord blood in thalassemic groups. IV].
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Female↗
[Genetic and biochemical studies in 4 siblings with Wilson's disease].
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Adolescent↗