Ineffective Erythropoiesis in β-Thalassemia by Jean-Antoine Ribeil, Jean-Benoit Arlet, Michael Dussiot, Ivan Cruz Moura, Geneviève Courtois, Olivier Hermine

“…In humans, β-thalassemia dyserythropoiesis is characterized by expansion of early erythroid precursors and erythroid progenitors and then ineffective erythropoiesis. …”
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Nonsurgical Approaches for Managing Hypersplenism in Thalassemia by Abdullah Talal Almohammadi

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Physiopathology of Bone Modifications in β-Thalassemia by Carlo Perisano, Emanuele Marzetti, Maria Silvia Spinelli, Cinzia Anna Maria Callà, Calogero Graci, Giulio Maccauro

“…β-thalassemia major (βTM) or Cooley anemia is characterized by significantly reduced or absent synthesis of β-globin chains, which induces important pathologic consequences including hemolytic anemia, altered erythropoiesis, and bone marrow overstimulation. …”
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Body Composition in Adult Patients with Thalassemia Major by Marianna Vlychou, Evangelos Alexiou, Paschalis Thriskos, Ioannis Fezoulidis, Katerina Vassiou

“…To assess body composition in adult male and female patients with thalassemia major by dual-energy X-ray absorptiometry (DXA) and to compare the findings with a group of healthy age-matched controls. …”
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Cardiac injury caused by iron overload in thalassemia by Chunxi Fu, Chunxi Fu, Xue Yang, Xue Yang

Subjects: “…β-thalassemia…”
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Nutritional Status of Children with Beta Thalassemia Major by Dhara Bipin Joshi, Uma Siddharth Nayak

“…Children with beta thalassemia major are at risk for poor nutritional status, which can lead to signifcant health problems. …”
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Extracellular vesicles in thalassemia: Mechanisms, implications, and therapeutic potential by Shahzad Ali Jiskani

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Estimation of CD8 Parameter Level in Thalassemia Patients by Sajad Abd-Alsahib, Ali Abd-Alhussein, Yousor Majid Jameel

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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

“…Background. β-thalassemia is an inherited blood disorder that affects the production of hemoglobin molecules owing to the reduction or absence of beta chains. …”
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Comprehensive analysis of a-and b-thalassemia genotypes and hematologic phenotypes by Heng Wang, Hai Huang, Yaping Chen, Xie Dan, Bangquan An, Shengwen Huang

Subjects: “…thalassemia…”
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Studying Some Factors That Increase the Risk of Thalassemia in The City of Baquba by Sara Fawzi Sahm

Subjects: “…Thalassemia…”
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Sickle Cell Beta-Plus Thalassemia with Subcapsular Hematoma of the Spleen by Suyash Dahal, Sumit Dahal, Dipesh K. C. Ghimire, Ebad Ur Rahman, Eliza Sharma

“…While splenic complications like hypersplenism, sequestration crisis, and infarction are commonly reported in sickle cell variants like sickle cell beta-plus thalassemia, splenic rupture with hematoma is rare. …”
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The distribution and spectrum of thalassemia variants in GUIYANG region, southern China by Xuanyin Zhao, Zhiyu You, Yunyan Deng, Yi Zhou, Dongyang Deng, Jian Quan, Fang Chen, Zhimei Yan, Ya Qi, Leilei Chen, Fang Xiang, Weixian Zheng, Ruyi Zhang

Subjects: “…Thalassemia…”
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PSYCHOSOCIAL ILLNESS IN CHILDREN WITH THALASSEMIA: A CASE-CONTROL STUDY by Erum Afzal, Muhammad Aslam Sheikh, Sajjad Hussain Bhaba, Tanveer Ahmed, Imran Iqbal, Muhammad Khalid Iqbal

Subjects: “…Psychosocial problems, Intellectual issues, Thalassemia children, Pediatric symptom checklist…”
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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

Subjects: “…β- thalassemia…”
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Factors contributing to anxiety in adolescents surviving thalassemia major in Indonesia by Henny Suzana Mediani, Novitasari Tsamrotul Fuadah

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𝛽-Thalassemia: HiJAKing Ineffective Erythropoiesis and Iron Overload by Luca Melchiori, Sara Gardenghi, Stefano Rivella

“…𝛽-thalassemia encompasses a group of monogenic diseases that have in common defective synthesis of 𝛽-globin. …”
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THALIDOMIDE AMELIORATES ERYTHROPOIESIS AND IRON HOMEOSTASIS IN TRANSFUSION-DEPENDENT β-THALASSEMIA by Kun Yang, Jian Xiao

“…Thalidomide is a therapeutic option for patients with β-­thalassemia by increasing fetal hemoglobin and thereby reducing the requirement for blood transfusions. …”
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Adropin and Preptin Levels in β-Thalassemia Major Complications in Babylon Province by Zinah Abbass Ali, Samar Hasan Shammar

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