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03/2013
Background: β-thalassaemia is one of the most common single-gene disorders worldwide. Each ethnic population has its own common mutations, accounting for the... 
Molecular diagnostics | β-globin gene mutations | β-thalassaemia | MARMS
Web Resource
Indian Journal of Medical Research, ISSN 0971-5916, 2015, Volume 141, Issue May, pp. 505 - 508
Journal Article
International Journal of Laboratory Hematology, ISSN 1751-5521, 04/2019, Volume 41, Issue 2, pp. 262 - 270
The accurate determination of Hb A is a key marker when screening for a β-thalassaemia carrier. Data from external quality assessment (EQA) exercises have... 
Hb A | standardization | external quality assessment | reference material | β-thalassaemia
Journal Article
Indian Journal of Medical Research, ISSN 0971-5916, 10/2011, Volume 134, Issue 10, pp. 498 - 506
Journal Article
Growth Factors, ISSN 0897-7194, 07/2018, Volume 36, Issue 3-4, pp. 178 - 185
Bone disorders and disturbed calcium (Ca) homeostasis are common disorders in β-thalassaemia major (β-TM). In the present study, two bone related markers are... 
iron | calcium | β-thalassaemia major | CAPS | FGFR2
Journal Article
International Journal of Pediatric Otorhinolaryngology, ISSN 0165-5876, 10/2019, Volume 125, pp. 59 - 65
Among children with β-thalassaemia, skeletal changes and abnormalities, such as decreased volume or obliteration of the sinus, result primarily from... 
β-Thalassaemia | Cone beam computed tomography | Skeletal changes | Maxillary sinus | 3D evaluation | Index Medicus
Journal Article
Blood Cells, Molecules and Diseases, ISSN 1079-9796, 07/2019, Volume 77, pp. 137 - 141
The clinical manifestations of Sickle Cell Disease (SCD) include episodes of vascular occlusion, chronic hemolytic anemia and frequent infections. GDF-15, a... 
Sickle Cell Disease | βthalassaemia | Endotheial dysfunction | GDF-15 | ADAMTS-13 | GDF15 | HYDROXYUREA | beta thalassaemia | HEMATOLOGY | VON-WILLEBRAND-FACTOR
Journal Article
Indian Journal of Medical Research, ISSN 0971-5916, 04/2016, Volume 143, Issue April, pp. 449 - 454
Journal Article
British Journal of Haematology, ISSN 0007-1048, 05/2008, Volume 141, Issue 3, pp. 407 - 410
Summary Although the β thalassaemia trait affects millions of people worldwide, there have been no controlled studies to determine whether it is associated... 
thalassaemia trait | β thalassaemia | anaemia
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
European Biophysics Journal, ISSN 0175-7571, 10/2019, Volume 48, Issue 7, pp. 635 - 643
In this work, wild-type and heterozygous β-thalassaemic mice were enriched with 57Fe via gastrointestinal absorption to characterize in greater detail the iron... 
Biochemistry, general | 57 Fe enrichment | Membrane Biology | Neurobiology | Ferritin | Blood | Cell Biology | Life Sciences | Mössbauer spectroscopy | β-Thalassaemia | Mice | Biological and Medical Physics, Biophysics | Nanotechnology | Enrichment | Spectroscopy | Iron 57 | Anemia | Thalassemia | Iron | Reticulocytes | Spectrum analysis | Mossbauer spectroscopy | Hemoglobin | Coordination compounds
Journal Article
International Journal of Laboratory Hematology, ISSN 1751-5521, 04/2019, Volume 41, Issue 2, pp. 262 - 270
The WHO IRR was analysed for Hb A.sub.2 concentration by 52 laboratories using a representative range of high-performance liquid chromatography and capillary... 
Hb A | standardization | 2 | external quality assessment | β‐thalassaemia | reference material | Chemical tests and reagents | Analysis | High performance liquid chromatography | Public health | Thalassemia | Liquid chromatography | Quantitation | Capillary electrophoresis | Quality control | Index Medicus
Journal Article
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