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12/2010
Introduction : India is an ethnically diverse country with an approximate population of 1.2 billion. The frequency of beta-thalassemia trait (βTT) has... 
β-thalassemia trait | Hemoglobinopathies | India
Web Resource
03/2013
Background: First and second-degree heart blocks are partly common rhythm disorders in thalassemic patients but complete heart block is a very rare... 
Iron overload | Arrhythmia | β-Thalassemia | Cardiomyopathy
Web Resource
Molecular characterization of mutations causing β-thalassemia in Faisalabad Pakistan using the amplification refractory mutation system (ARMS-PCR), 12/2005
BACKGROUND: Faisalabad is the third biggest city of Pakistan. Majority of the population is Punjabi while other ethnic groups are in minority. AIMS: The... 
Pakistan | mutations | Faisalabad | β -thalassemia | ARMS-PCR | mutations detection
Journal
04/2011
Background: Sickle cell-β thalassemia (HbS-β thalassemia) is a sickling disorder of varying severity, which results from compound heterozygosity for sickle... 
HbS- β thalassemia | clinical | mutations | framework | India
Web Resource
07/2011
Objective: Beta-thalassemia major is an autosomal recessive disease causing severe and hemolytic anemia, which begins about 2-6 months after birth. Iron... 
Antioxidants | Oxidative Stress | Ferritin | Uric Acid | β-Thalassemia Major
Web Resource
05/2011
Background: β-thalassemia is the most common hereditary disease in Iran and more than 2 million carriers of the β-thalassemia mutant gene are living in this... 
Oligohydramnios | Pregnancy outcome | Minor β-thalassemia | Gestational diabetes mellitus
Web Resource
Genomics, ISSN 0888-7543, 2019
The master erythroid regulator KLF1,plays a pivotal role during erythroid lineage development by regulating the expression of many erythroid genes. Variations... 
KLF1 mutation | Raised HbF | Sickle cell anemia | β-thalassemia | India
Journal Article
Clinical Biochemistry, ISSN 0009-9120, 03/2019, Volume 65, pp. 24 - 28
Objective: The aims of this study were to establish the reference intervals for HbA2 and HbF in a Guizhou population of reproductive age, and to determine the... 
Cut-off value | Reference interval | HbF | HbA | β-thalassemia
Journal Article
Japanese Journal of Infectious Diseases, ISSN 1344-6304, 2018
Cytomegalovirus (CMV) rarely causes disease in immunocompetent individuals but may cause severe disease in immunocompromised patients. We report the case of a... 
Cytomegalovirus | blood transfusion | pneumonitis | β-thalassemia | splenectomy
Journal Article
Blood Cells, Molecules and Diseases, ISSN 1079-9796, 03/2016, Volume 57, pp. 91 - 96
β-Thalassemia major (BTM) is considered the most common hemoglobinopathy in Egypt and is one of the major health problems in our locality. We investigated the... 
β-Thalassemia major | Alloantibodies | Regulatory B cells
Journal Article
Clinical Chemistry and Laboratory Medicine, ISSN 1434-6621, 08/2018, Volume 56, Issue 9, pp. 1507 - 1513
Journal Article
Revue de Medecine Interne, ISSN 0248-8663, 01/2016, Volume 37, Issue 1, pp. 5 - 12
Introduction: Symptomatic extramedullary hematopoiesis (EH) is a rare but potentially severe phenomenon which occurs in β-thalassemia. There are no treatment... 
Anemia | Extramedullary hematopoiesis | β-thalassemia
Journal Article
Journal de Mycologie Medicale, ISSN 1156-5233, 12/2017, Volume 27, Issue 4, pp. 582 - 585
Candida spp. vertebral osteomyelitis is rare. Clinical presentation is unspecific. Diagnosis requires mycological culture of a biopsy specimen. Therapeutic... 
Vertebral osteomyelitis | Candida tropicalis | β-thalassemia
Journal Article
Clinical Laboratory, ISSN 1433-6510, 2019, Volume 65, Issue 5, pp. 877 - 879
A pregnant 30-year-old female in the 34th gestational week was admitted at University "Maichin Dom" Hospital prior to childbirth. The patient is diagnosed with... 
Pregnancy | Anemia | Hepcidin | β-thalassemia | Parvovirus B19
Journal Article
Hiroshima Journal of Medical Sciences, ISSN 0018-2052, 05/2018, Volume 67, pp. 78 - 83
Journal Article
Clinical Biochemistry, ISSN 0009-9120, 12/2009, Volume 42, Issue 18, pp. 1786 - 1796
Background and objective: The inherited hemoglobinopathies are a large group of disorders that include thalassemias and hemoglobin variants. Accurate... 
α-thalassemia | borderline | Hemoglobin A | Hemoglobinopathy screening | HbA | β-thalassemia
Journal Article
Clinica Chimica Acta, ISSN 0009-8981, 02/2018, Volume 477, pp. 60 - 65
Most of the current methods used for the determination of HbA seem not well aligned. A comparison among the best performing techniques and the commutability of... 
Commutability | HbA2 | Multicenter evaluation | β-Thalassemia | Standardization | Harmonization | HbA | Index Medicus
Journal Article
Blood Cells, Molecules, and Diseases, ISSN 1079-9796, 08/2011, Volume 47, Issue 2, pp. 120 - 124
In order to update the molecular basis of β-thalassemia and describe hematological features among different mutations and the concurrent of β- and... 
Northeast Thailand | Hemoglobin A2 | β-thalassemia | Hemoglobin F
Journal Article
Clinical Biochemistry, ISSN 0009-9120, 03/2019, Volume 65, pp. 24 - 28
The aims of this study were to establish the reference intervals for HbA2 and HbF in a Guizhou population of reproductive age, and to determine the cut-off... 
HbA2 | Cut-off value | Reference interval | HbF | β-thalassemia | Index Medicus
Journal Article
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