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HEALTH AND QUALITY OF LIFE OUTCOMES, ISSN 1477-7525, 08/2019, Volume 17, Issue 1, pp. 137 - 13
Background Thalassaemia is a chronic disease without an effective cure in a majority. The clinical management has improved considerably during recent years;... 
Haemoglobin E beta-thalassaemia | Transfusion | beta-Thalassaemia major | DISEASE | HEALTH CARE SCIENCES & SERVICES | Thalassaemia | HEALTH POLICY & SERVICES | Quality of life | β-Thalassaemia major | Haemoglobin E β-thalassaemia
Journal Article
SIGHT THREATENING RETINOPATHY IN AN EIGHT YEAR OLD NIGERIAN MALE WITH SICKLE CELL β° THALASSAEMIA: CASE REPORT, 2004
Sight threatening changes in the retina are a well-recognized complication of sickle cell disease (SCD). However they usually occur in older patients with... 
Medicine | sickle, cell, retinopathy, beta thalassaemia am04035
Journal
British Journal of Haematology, ISSN 0007-1048, 03/2016, Volume 172, Issue 6, pp. 958 - 965
Summary Two 21‐year old dizygotic twin men of Iraqi descent were homozygous for HBB codon 8, deletion of two nucleotides (–AA) frame‐shift β0‐thalassaemia... 
HBS1L‐MYB intergenic polymorphism | α‐Thalassaemia | β0‐Thalassaemia | HbF quantitative trait loci | fetal haemoglobin | Thalassaemia | Fetal haemoglobin | HBS1L-MYB intergenic polymorphism | α-Thalassaemia
Journal Article
Indian Journal of Medical Research, ISSN 0971-5916, 2015, Volume 141, Issue May, pp. 505 - 508
Journal Article
Indian Journal of Medical Research, ISSN 0971-5916, 10/2011, Volume 134, Issue 10, pp. 498 - 506
Journal Article
International Journal of Laboratory Hematology, ISSN 1751-5521, 12/2016, Volume 38, Issue 6, pp. 610 - 615
Summary Introduction Mutations in the δ‐globin gene are not pathogenically relevant, but co‐inheritance of δ‐globin variants along with β‐globin gene defects... 
δ‐thalassaemia | β‐globin gene | β‐thalassaemia | low HbA2 level | India | β-globin gene | δ-thalassaemia | low HbA | level | β-thalassaemia | Case studies | Gene mutations | Analysis | Genes | Genetic research | Nucleotide sequencing | DNA sequencing
Journal Article
THROMBOSIS AND HAEMOSTASIS, ISSN 0340-6245, 10/2006, Volume 96, Issue 4, pp. 488 - 491
Beta-thalassaemia is a congenital haemolytic anaemia characterized by partial (intermedia, TI) or complete (major, TM) deficiency in the production of... 
thalassaemia major | thrombosis | THALASSEMIA-INTERMEDIA | ENDOTHELIAL-CELLS | RISK | PERIPHERAL VASCULAR DISEASE | BETA-THALASSEMIA | HEMATOLOGY | thalassaemia intermedia | PULMONARY THROMBOEMBOLISM
Journal Article
1983, Methods in hematology, ISBN 0443025657, Volume 6, 166
Book
British Journal of Haematology, ISSN 0007-1048, 01/2004, Volume 124, Issue 2, pp. 224 - 231
Journal Article
Journal of Medical Screening, ISSN 0969-1413, 12/2014, Volume 21, Issue 4, pp. 167 - 171
Objective To determine the prevalence of α-thalassaemia in β-thalassaemia individuals in a Chinese population. Methods The standard diagnostic marker for... 
Co-inheritance | α-thalassaemia | Prenatal screening | β-thalassaemia | PHENOTYPE | PREVENTION | CARRIERS | INTERMEDIA | DELETION | beta-thalassaemia | HYDROPS-FETALIS | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | GLOBIN GENE | H DISEASE | alpha-thalassaemia | prenatal screening | Thalassemia | Genetic aspects | Prenatal diagnosis | Methods
Journal Article
Journal of the Pakistan Medical Association, ISSN 0030-9982, 09/2017, Volume 67, Issue 9, pp. 1434 - 1437
The present study was designed to assess the Knowledge, Attitude and Practices (KAP) of the parents of beta-thalassaemia children (410) selected from public... 
KAP | Premarital screening | β-thalassaemia | Thalassaemia children | MEDICINE, RESEARCH & EXPERIMENTAL | beta-thalassaemia | MEDICINE, GENERAL & INTERNAL
Journal Article
British Journal of Haematology, ISSN 0007-1048, 07/2017, Volume 178, Issue 1, pp. 130 - 136
Journal Article
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