Nutritional Status of Children with Beta Thalassemia Major by Dhara Bipin Joshi, Uma Siddharth Nayak

“… Background. Children with beta thalassemia major are at risk for poor nutritional status, which can lead to signifcant health problems. …”
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A Smart Chatbot for Interactive Management in Beta Thalassemia Patients by Alma Mohammed Alturaiki, Haneen Reda Banjar, Ahmed Salleh Barefah, Salwa Abdulrahman Alnajjar, Salwa Hindawi

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Infusion of Autologous Retrodifferentiated Stem Cells into Patients with Beta-Thalassemia by Ilham Saleh Abuljadayel, Tasnim Ahsan, Huma Quereshi, Shakil Rizvi, Tamseela Ahmed, Sabiha Mirza Khan, Jawaid Akhtar, Ghazi Dhoot

“…Beta-thalassemia is a genetic, red blood cell disorder affecting the beta-globin chain of the adult hemoglobin gene. …”
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Biochemical Status of Beta-Thalassemia Major Patients in Erbil City by Omar Surchi, Sarkawt Ali

“…Patients and method: In this research 40 patients with beta thalassemia major, 20 Female and 20 Male (age ranged from 10 to 38 years), and 40 control subjects 20 Female and 20 Male (age ranged from 9 to 33 years) were studied. …”
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Deferoxamine Intradermal Delivery Patch for Treatment of a Beta-Thalassemia Wound by David Perrault, MD, Arhana Chattopadhyay, MD, Dharshan Sivaraj, BS, Derrick Wan, MD, Kellen Chen, PhD, Geoffrey Gurtner, MD, Subhro Sen, MD

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Beta-Thalassemia in Iran: New Insight into the Role of Genetic Admixture and Migration by Ali Reza Rezaee, Mohammad Mehdi Banoei, Elham Khalili, Massoud Houshmand

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Hematological Parameters in Individuals with Beta Thalassemia Trait in South Sumatra, Indonesia by Dian Puspita Sari, Pustika Amalia Wahidiyat, Iswari Setianingsih, Ina S. Timan, Djajadiman Gatot, Aria Kekalih

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Beta-Thalassemia Major and Female Fertility: The Role of Iron and Iron-Induced Oxidative Stress by Paraskevi Roussou, Nikolaos J. Tsagarakis, Dimitrios Kountouras, Sarantis Livadas, Evanthia Diamanti-Kandarakis

“…Endocrine complications due to haemosiderosis are present in a significant number of patients with beta-thalassemia major (BTM) worldwide and often become barriers in their desire for parenthood. …”
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Rare coinheritance of hemoglobin vancleave with severe beta-thalassemia mutation in a patient with secondary erythrocytosis by Nur Aisyah Aziz, Nurul Hidayah Musa, Melina Mathews, Komalah Thevii Rajenderan, Faidatul Syazlin Abdul Hamid, Syahzuwan Hassan, Syahira Lazira Omar, Wan Nurul Afiqha Binti Wan Yusoff, Melanie Ling Binti Mohd Din, Nurul Amira Binti Jamaludin, Wan Rohani Wan Taib, Ezalia Esa, Norafiza Mohd Yasin

“…This report highlights the importance of sequencing in the differential diagnosis of beta-thalassemia syndrome in Malaysia.…”
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Study of platelet activation, hypercoagulable state, and pulmonary hypertension in patients with transfusion-dependent beta-thalassemia by Lanja Othman Haji, Ranan Kardagh Polus, Nawsherwan Sadiq Mohammed

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Study of vascular endothelial dysfunction in children with beta-thalassemia major before and after quercetin therapy by Fatma Al Zahraa Sherai, Maaly Mabrouk, Ibrahim Badraia, Adel Hagag, Eman Elaskary

“…Abstract Background Beta-thalassemia stands as an autosomal recessive disorder that occurs as a result of a defect in the beta-globin chain synthesis of hemoglobin. …”
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Assessment of cardiac iron deposition and genotypic classification in pediatric beta-thalassemia major: the role of cardiac MRI by Siqi Zhang, Wen Zhao, Longwei Sun, Guohua Liang, Xiaodong Wang, Hongwu Zeng

“…Abstract Background Beta thalassemia major (β-TM) is a severe genetic anemia with considerable phenotypic heterogeneity. …”
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A scoping review on the obstacles faced by beta thalassemia major patients in Pakistan- Matter of policy investment by Ali Hussain Ansari, Saqib Hussain Ansari, Mubarak Jabeen Salman, Muhammad Usman Hussain Ansari, Rawshan Jabeen

Subjects: “…beta thalassemia…”
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Arrhythmias and Sudden Cardiac Death in Beta-Thalassemia Major Patients: Noninvasive Diagnostic Tools and Early Markers by Vincenzo Russo, Enrico Melillo, Andrea A. Papa, Anna Rago, Celeste Chamberland, Gerardo Nigro

“…Beta-thalassemias are a group of inherited, autosomal recessive diseases, characterized by reduced or absent synthesis of beta-globin chains of the hemoglobin tetramer, resulting in variable phenotypes, ranging from clinically asymptomatic individuals to severe anemia. …”
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Anti-Thyroid Peroxidase Antibodies and Male Gender Are Associated with Diabetes Occurrence in Patients with Beta-Thalassemia Major by Giovanni M. Pes, Francesco Tolu, Maria P. Dore

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Thyroid Function in Chronically Transfused Children with Beta Thalassemia Major: A Cross-Sectional Hospital Based Study by Suraj Haridas Upadya, M. S. Rukmini, Sowmya Sundararajan, B. Shantharam Baliga, Nutan Kamath

“…The frequency of hypothyroidism in Beta Thalassemia Major (BTM) children ranges from 6 to 30 %. …”
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Association between Alpha- Klotho Protein, Calcium, and Phosphate concentrations in Adult Iraqi Patients with Beta-Thalassemia Major by Ahmed J. Kadhim, Hedef D. El-Yaseen, Ali M. Jawad

“… Background: Beta-thalassemia major is a prevalent global condition characterized by a rapid breakdown of red blood cells. …”
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Investigating Oxidative Stress and Antioxidant Dynamics in Beta-thalassemia Major: A Comparative Study from Al-Diwaniyah, Iraq by Hadeer Hayder Inteek, Shaymaa Rabeea Madhkhoor

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An Observational Study of Glomerular Functions in Beta-thalassemia Major Children by Schwartz Formula and Technetium 99m Diethylenetriaminepentaacetic Acid Renogram by Sukanta Mandal, Tathagata Bose, Rachna Gulati, Manish Singh Ahuja

Subjects: “…beta-thalassemia major…”
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Correlation of Oxidative Stress with Serum Trace Element Levels and Antioxidant Enzyme Status in Beta Thalassemia Major Patients: A Review of the Literature by Q. Shazia, Z. H. Mohammad, Taibur Rahman, Hossain Uddin Shekhar

“…Beta thalassemia major is an inherited disease resulting from reduction or total lack of beta globin chains. …”
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