1-15 of 15
Keywords: α-Thalassaemia
Close
Follow your search
Access your saved searches in your account

Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1971) 46 (3): 149–156.
Published Online: 05 March 2009
... in unusually high percentage in heterozygotes (Hb A + Hb Gα Philadelphia). It is proposed that the gene for this variant is linked with one for α-thalassaemia. α-thalassaemia Haemoglobinopathies Hb Ga Philadelphia © 1971 S. Karger AG, Basel 1971 Copyright / Drug Dosage / Disclaimer Copyright...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1971) 46 (2): 106–120.
Published Online: 05 March 2009
... or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. α-Thalassaemia Haemoglobin Bart’s Haemoglobin H disease Haemoglobinopathies Acta...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1979) 61 (2): 114–119.
Published Online: 03 March 2009
... for inclusion bodies of Hb H did not suggest α-thalassaemia. The mothers of these babies do not show any evidence of α -thalassaemia. It is suggested that the presence of Hb Barts in samples of cord blood is not due to the presence of α -thalassaemia in the Tanzanian population. 31 05 1977 25 05 1978...
Journal Articles
Journal Articles
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1979) 61 (1): 33–38.
Published Online: 03 March 2009
... no haematological or electrophoretic signs of α -thalassaemia. The significance of these findings is discussed in the light of previously reported studies on various Negro groups. 4 10 1977 11 07 1978 3 3 2009 Acta haemat. 61: 33-38 (1979) Hb Bart s and its Significance in the South African...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1977) 57 (2): 109–115.
Published Online: 03 March 2009
.... Although this is the first report of this condition in this country it is pointed out that one may see more such cases in the future if one is aware of this condition since Hb E, α-thalassaemia and Hb CoSp all occur at significant frequencies in this country. α-Thalassaemia Hb CoSp Hb E...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1976) 55 (1): 36–39.
Published Online: 03 March 2009
...G. Martinez; B. Colombo The frequency of α-thalassaemia has been determined by the analysis of Hb Barts in 650 newborns; 4.46% of them showed high levels of Hb Barts. The incidence of newborns with different levels of Hb Barts (1–2, 5 and 25%, respectively) and the frequency of the α-thalassaemia...
Journal Articles
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1987) 78 (2-3): 173–179.
Published Online: 25 February 2009
...A.V.S. Hill; J. Flint; D.J. Weatherall; J.B. Clegg Recent population genetic studies of the distribution of α + -thalassaemia in Melanesia using DNA analysis have provided strong support for the hypothesis that high frequencies of this genetic disorder are the result of natural selection by malaria...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1987) 77 (1): 60–61.
Published Online: 25 February 2009
... or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Fetal haemoglobin Priapism Sickle cell disease α -Thalassaemia 11 07 1986 29 09 1986 25 2 2009 Actahaemat. 77: 60-61 (1987) © 1987 S. Karger AG. Basel 0001...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1985) 73 (3): 159–162.
Published Online: 25 February 2009
... not associated with detectable levels of Hb Barts. Mapping of the g-globin locus in three subjects with HbH disease revealed the presence of the – – SEA / α -thalassaemia determinant in this population. 1 11 1984 4 02 1985 25 2 2009 © 1985 S. Karger AG, Basel 1985 Copyright / Drug Dosage...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1984) 71 (4): 247–250.
Published Online: 25 February 2009
... was homozygous for α + -thalassaemia (genotype α- / α-), whereas the other had a full complement of α-globin genes. Both showed markedly elevated levels of Hb F. The maintenance of high levels of Hb F is the most probable explanation for the moderate clinical expression of the disorder in these patients. Hb F...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1994) 91 (4): 201–205.
Published Online: 18 February 2009
...Chi-kong Li; Margaret Heung-ling Ng; Kam-lau Cheung; Tai-kwan Lam; Matthew Ming-kong Shing We report here a family of patients with coexistent hereditary spherocytosis and α-thalassaemia. The different clinical presentations of the family members were affected by the severity of the α-thalassaemia...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1992) 88 (4): 165–169.
Published Online: 18 February 2009
...A.A. Al-Saleh; S. Hussain The α-thalassaemias are group of inherited anaemias. Their severity is known to increase with the number of α-globin genes deleted. Employing different types of restriction enzymes, we found that α-thalassaemia-2 are more common than held previously. On the basis of our...