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Keywords: α-Thalassemia
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Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (2020) 143 (5): 432–437.
Published Online: 14 January 2020
... at our tertiary center between 2007 and 2017 and diagnosed as heterozygotes for the –α 3.7 deletion. Additional α-thalassemia mutations, iron deficiency anemia, and β-thalassemia were ruled out. Laboratory parameters were compared to age- and sex-matched reference values. Results: The –α 3.7 carriers had...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (2016) 135 (4): 200–207.
Published Online: 28 January 2016
... responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. α-Thalassemia Systolic function Diastolic function Ferritin Iron overload Anemia The α-thalassemias arise from deletions or mutations...
Journal Articles
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (2010) 123 (4): 207–209.
Published Online: 16 April 2010
...Yu Yang; Dong-Zhi Li A fetus at risk for α-thalassemia presented with cardiomegaly without evidence of anemia. Invasive testing demonstrated the diagnosis of homozygous α-thalassemia-1 with a normal-range hemoglobin (Hb) level. We suggest that in the prenatal detection of homozygous α-thalassemia-1...
Journal Articles
Journal Articles
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1971) 45 (6): 365–368.
Published Online: 05 March 2009
...A.P. Gelpi The percentage of Hb S in hemolysates from 109 Saudi Arab males was found to range from 18–47%, with a mean of 33%, an obvious mode at 32–34% and clear skewing of the overall pattern toward lower values. A tentative explanation of this finding is the concurrence of the α-thalassemia...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1981) 65 (4): 240–246.
Published Online: 27 February 2009
... which contained more than 0.5% Hb Bart’s. These findings suggest that elevated Hb Bart’s levels in the Algerian population are due to the presence of α-thalassemia. Acta haemat. 65: 240-246 (1981) Hemoglobin Bart s in Northern Algeria 7. Henni", D. Bachir", P. Tabone", P. Jurdic", J. Godet'1, P. Colonna...
Journal Articles
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1981) 65 (1): 26–31.
Published Online: 27 February 2009
...P. Tabone; T. Henni; M. Belhani; P. Colonna; G. Verdier; J. Godet A case of Hb H disease from Algeria was studied at the genetic and molecular level in order to delineate the pattern of α-thalassemia in the Mediterranean population. The family study indicated that both parents had the hematological...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1980) 64 (3): 136–140.
Published Online: 27 February 2009
... in the blood for the remaining 2. The decrease in the relative synthesis of α-globin on erythroid cell maturation may relate to the molecular basis of α-thalassemia in the Middle East. Acta haemta. 64: 136-140 (1980) Balanced Bone Marrow Globin Synthesis in Mideastern a-Thalassemia R. Zaizov, M. Steinherz, B...
Journal Articles
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1985) 74 (3): 186–188.
Published Online: 25 February 2009
... fragment. Mild hematological alterations were present. These data indicate that also in the Cuban population the α G Philadelphia locus is linked to a deletional α -thalassemia 27 09 1985 21 10 1985 25 2 2009 © 1985 S. Karger AG, Basel 1985 Copyright / Drug Dosage / Disclaimer...
Journal Articles
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1985) 73 (3): 181–182.
Published Online: 25 February 2009
... α -Thalassemia Acta haemat. 73: 181-182(1985) © 1985 S. Karger AG, Basel 0001-5792/85/0733-0181 $ 2.75/0 Priapism in Association with Sickle Cell Anemia in Saudi Arabia1 Baker Al-Awamy, Saud A. Taha, Mahtab A. Naeem Sickle Cell Anemia Group, King Faisal University, Dammam, Saudi Arabia Key Words...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1990) 84 (3): 135–138.
Published Online: 20 February 2009
... comparable to those seen in patients with a homozygosity for the -29 mutation or with the combination of this β + -thalassemia and Hb S. An α-thalassemia-2 heterozygosity (-3.7 kb deletion) was present in 2 patients. Their hematological data were improved over those for the patients with four α globin genes...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1989) 82 (2): 64–68.
Published Online: 20 February 2009
...Hong-Wen Peng; Kong-Bung Choo; Chao-Hung Ho; Ming-Shyen Yen; Wan-Ying Liung; Chung-King Lin; Zaw-Ling Yang; Heung-Tat Ng; King-Nien Ching; Shou-Hwa Han In a gene mapping study on 217 newborn babies in Taiwan with α- and ζ-globin probes, we have observed 4 cases (1.84%) of α-thalassemia-2...
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1992) 87 (3): 145–147.
Published Online: 19 February 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-Gene deletion HbH disease α-Thalassemia Case Report Acta Haematol 1992;87:145-147...
Journal Articles
Journal Articles
Subject Area:
Hematology , Oncology
Acta Haematol (1996) 96 (3): 150–154.
Published Online: 17 February 2009
... α-thal trait did not have severe recurrent infections and none had gallstones. The high frequencies of the Saudi Arabia/India βs haplotype and α-thalassemia trait contribute to the mild nature of SS disease among Kuwaiti Arabs comparable to that in eastern Saudi Arabia. 29 08 1995 11 12...