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Keywords: Hb F
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Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (2010) 123 (3): 135–139.
Published Online: 21 January 2010
...Adekunle Adekile; Ali Mullah-Ali; Najwa Ali Akar Hemoglobin (Hb) SD-Los Angeles compound heterozygotes usually have a severe clinical course although the effect of an elevated Hb F on the clinical phenotype has not been reported previously. We describe 5 Kuwaiti children with Hb SD associated...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1979) 62 (1): 45–50.
Published Online: 03 March 2009
... ± 0.04 expressed as glycine residue at position 136) than in full-term newborns (0.73 ± 0.06), while the incidence and the percentage of T γ -chains were clearly higher in the first group and overlap the values found in the Hb F from β -thalassemia homozygotes. On the basis of these data the authors...
Journal Articles
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1980) 63 (3): 146–150.
Published Online: 03 March 2009
... responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Hb F γ -Chain composition HPFH Negro type Acta haemat. 63: 146 150 (1980) Analysis of the y Chains in a Homozygote for H PFH Negro Type...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1983) 69 (4): 275–277.
Published Online: 26 February 2009
...Mitsuhiro Omine; Nobuaki Iwata; Tadashi Maekawa; Yuzo Ohba A 7-year-old boy with juvenile erythroleukemia is described, whose red cells demonstrated a high content of Hb F with fetal structure and yet contained carbonic anhydrase at adult red cell level. The findings seem to exemplify...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1987) 78 (1): 23–27.
Published Online: 25 February 2009
... 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. G γ nd A γ chains Gene mapping γ -Globin gene triplication Haplotypes Hb F Restriction enzymes α...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1986) 76 (4): 208–211.
Published Online: 25 February 2009
... to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. γ-Globin Hb F Hb F Sardinia Polymorphism Thalassaemia intermedia β + -Thalassaemia Acta haemat. 76: 208-211 (1986) © I986S. Karger AG, Basel 0001-5792/86/0764-0208...
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 (1985) 73 (3): 181–182.
Published Online: 25 February 2009
... that high Hb F levels and hypochromic microcytosis in Saudi patients might play an important role in preventing this complication. 4 01 1985 18 02 1985 25 2 2009 © 1985 S. Karger AG, Basel 1985 Copyright / Drug Dosage / Disclaimer Copyright: All rights reserved. No part...