Challenges in Glycemic Monitoring: Undetectable HbA1c Level in an Asymptomatic Patient With Hemoglobin E and Beta-Thalassemia Minor: A Case Report. [PDF]
Prawitasari D, Zuhri S, Fuadi R.
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Frequency of β-thalassemia minor in Ardabil province in 2017-2018 [PDF]
Background and Objective. Thalassemia is a genetic condition in which the patient's blood loses a large number of primary red blood cells and can not carry oxygen. Hemoglobin consists of two different chains called alpha and beta.
مظهری, نهاله +2 more
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Multisystem Complications in Non-Transfusion-Dependent β-Thalassemia Intermedia: A Case Highlighting the Need for Early Intervention. [PDF]
Aloosh O, Hosseini SE, Karimi M.
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β-Thalassemia Minor and Pregnancy Outcomes: Pathophysiology, Clinical Implications, and Management. [PDF]
Gerede A +9 more
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Diagnostic Challenges of Hemoglobin (Hb) Hekinan with deletional α<sup>0</sup>-thalassemia and β<sup>0</sup>-thalassemia During Prenatal Screening for Fetal Hb E/β-Thalassemia Risk. [PDF]
Chumnumsiriwath P +7 more
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Diagnosis and classification of thalassemia disease using machine learning: Comparative analysis of traditional models and a novel hybrid approach. [PDF]
Tekin H, Abbasoğulları EG, Günay FB.
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Genetic polymorphism of SNPs rs9399137 and rs4895441in HBS1L-MYB and SNP rs766432 in BCL11A among β-thalassemia Egyptian patients. [PDF]
Abdelrahman AA +4 more
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A Prospective Multi-Center Newborn Screening for Thalassemia by Comprehensive Analysis of Thalassemia Alleles (CATSA) Based on Single Molecule Real-Time Sequencing in Guangxi, China. [PDF]
Xia A +12 more
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Addressing Obstetric and Gynecologic Needs in Thalassemia. [PDF]
Vlachodimitropoulou E +9 more
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Development and Internal Validation of a Machine Learning-Based Model for Thalassemia Identification Using Complete Blood Count Parameters. [PDF]
Yin P, Tan J, Hong H.
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