Epidemiological profile of common haemoglobinopathies in Arab countries
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Unravelling the impact of ethnicity on health in Europe: the HELIUS studyMolecular Characterization of β-Thalassemia in Nineveh Province Illustrates the Relative Heterogeneity of Mutation Distributions in Northern Iraq.Diagnostic performance of HbA1c for diabetes in Arab vs. European populations: a systematic review and meta-analysis.Doppler-Defined Pulmonary Hypertension in Sickle Cell Anemia in Kurdistan, Iraq.β-Thalassemia Distribution in the Old World: an Ancient Disease Seen from a Historical Standpoint.β-globin genes: mutation hot-spots in the global thalassemia belt.The Effect of Hydroxyurea Therapy in Bahraini Sickle Cell Disease PatientsKnowledge and Attitudes Toward Mandatory Premarital Screening Among University Students in North Jordan.Frequencies and phenotypic consequences of association of α- and β-thalassemia alleles with sickle-cell disease in Bahrain.Predictors of Red Cell Alloimmunization in Kurdish Multi Transfused Patients with Hemoglobinopathies in Iraq.The Molecular Basis of α-Thalassemia in the Qatari Pediatric Population.The Start-Up of the first Hematopoietic Stem Cell Transplantation Center in the Iraqi Kurdistan: a Capacity-Building Cooperative Project by the Hiwa Cancer Hospital, Sulaymaniyah, and the Italian Agency for Development Cooperation: an Innovative AppAssociation of erythrocytes antioxidant enzymes and their cofactors with markers of oxidative stress in patients with sickle cell anemia.Detection of nine Mediterranean β-thalassemia mutations in Palestinians using three restriction enzyme digest panels: a reliable method for developing countries.Impact of war on child health in northern Syria: the experience of Médecins Sans Frontières.KLF1 gene and borderline hemoglobin A2 in Saudi population.New Insights on β-Thalassemia in the Palestinian Population of Gaza: High Frequency and Milder Phenotype Among Homozygous IVS-I-1 (HBB: c.92+1G>A) Patients with High Levels of Hb F.Molecular spectrum of α-globin gene mutations in the Aegean region of Turkey: first observation of three α-globin gene mutations in the Turkish population.[Medical care for refugees in Germany].Novel 31.2 kb α0 Deletion in a Palestinian Family with α-Thalassemia.The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β0-thalassaemia homozygotes
P2860
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P2860
Epidemiological profile of common haemoglobinopathies in Arab countries
description
2012 nî lūn-bûn
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2012年の論文
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2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
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2012年论文
@zh-cn
name
Epidemiological profile of common haemoglobinopathies in Arab countries
@en
type
label
Epidemiological profile of common haemoglobinopathies in Arab countries
@en
prefLabel
Epidemiological profile of common haemoglobinopathies in Arab countries
@en
P2860
P1476
Epidemiological profile of common haemoglobinopathies in Arab countries
@en
P2093
Hanan A Hamamy
Nasir A S Al-Allawi
P2860
P2888
P304
P356
10.1007/S12687-012-0127-8
P577
2012-12-08T00:00:00Z