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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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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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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β-Thalassemia: New Therapeutic Modalities, Genetics, Complications, and Quality of Life by Mehran Karimi, Sezaneh Haghpanah, Ali T. Taher, Maria Domenica Cappellini

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The Ongoing Challenge of Hematopoietic Stem Cell-Based Gene Therapy for β-Thalassemia by Ekati Drakopoulou, Eleni Papanikolaou, Nicholas P. Anagnou

“…β-thalassemia is characterized by reduced or absence of β-globin production, resulting in anemia. …”
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EFFECTS OF THALIDOMIDE ON ENDOTHELIAL ACTIVATION AND STRESS INDEX IN CHILDREN WITH Β-THALASSEMIA MAJOR by Kun Yang

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Genetic Correction of Sickle Cell Anemia and β-Thalassemia: Progress and New Perspective by Ajay Perumbeti, Punam Malik

“…Gene therapy for β-globinopathies, particularly β-thalassemia and sickle cell anemia, holds promise for the future as a definitive corrective approach for these common and debilitating disorders. …”
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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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Variation of DNA Repair Genes APE1 and RAD18 in β-Thalassemia Patients by Nawras Najah Jawad, Mona N. Al-Terehi

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Identification of β-globin gene mutations among transfusion-dependent β-thalassemia patients by Haidar Hussein Al-Fatlawi, Bassam Mahammad Hameed

Subjects: “…transfusion-dependent β-thalassemia…”
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Efficacy and safety of hydroxyurea therapy on patients with β-thalassemia: a systematic review and meta-analysis by Tianmin Huang, Huixian Jiang, Ganling Tang, Jingyi Li, Xiaoman Huang, Zhenguang Huang, Hongliang Zhang

Subjects: “…β-thalassemia…”
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Compliance with Deferoxamine Therapy among Transfusion-Dependent β-Thalassemia Patients in Nineveh Province, Northern Iraq by Ahmed Yahya Dallal Bashi, Zaid Muwafaq Younus, Muzahim Saeed Younis Al-Hamdani

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Potential Effects of Silymarin and Its Flavonolignan Components in Patients with β-Thalassemia Major: A Comprehensive Review in 2015 by Hadi Darvishi Khezri, Ebrahim Salehifar, Mehrnoush Kosaryan, Aily Aliasgharian, Hossein Jalali, Arash Hadian Amree

“…Major β-thalassemia (β-TM) is one of the most common inherited hemolytic types of anemia which is caused as a result of absent or reduced synthesis of β-globin chains of hemoglobin. …”
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Biochemical Markers of Bone Turnover in Patients with β-Thalassemia Major: A Single Center Study from Southern Pakistan by Sadia Sultan, Syed Mohammed Irfan, Syed Ijlal Ahmed

“…In this prospective cross-sectional study, 36 β-thalassemia major patients were enrolled from March 2012 to March 2014. …”
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Exploring the functional and immune landscape of E-β thalassemia patients through RNA sequencing of peripheral blood mononuclear cells by Nibedita Mitra, Prosanto Chowdhury, Anupam Basu

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Red blood cell alloimmunization among transfusion-dependent thalassemia major patients in Northeastern Iran by Leila Mobasheri, Tayyebeh Chahkandi, Amir Talebpour, Gholamreza Anani Sarab

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Current Genetic Epidemiology of 𝛽-Thalassemias and Structural Hemoglobin Variants in the Lazio Region (Central Italy) Following Recent Migration Movements by Antonio Amato, Maria Pia Cappabianca, Alessia Colosimo, Maria Perri, Paola Grisanti, Ivo Zaghis, Donatella Ponzini, Maria Lerone

“…The aim of this study was to describe the changing pattern of mutational spectrum of 𝛽-thalassemia (𝛽-thal) in the Lazio region (Central Italy), as consequence of recent demographic variations. …”
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Intracranial Blood Flow Velocity in Patients with β-Thalassemia Intermedia Using Transcranial Doppler Sonography: A Case-Control Study by Nahid Ashjazadeh, Sajad Emami, Peyman Petramfar, Ehsan Yaghoubi, Mehran Karimi

“…Introduction. Patients with β-thalassemia intermedia have a higher incidence of thromboembolic events compared to the general population. …”
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