| For: | Dordevic A, Mrakovcic-Sutic I, Pavlovic S, Ugrin M, Roganovic J. Beta thalassemia syndromes: New insights. World J Clin Cases 2025; 13(10): 100223 [PMID: 40191679 DOI: 10.12998/wjcc.v13.i10.100223] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v13/i10/100223.htm |
| Number | Citing Articles |
| 1 |
Mohammed N. Salman, Fouad Razzaq Al‐Burki, Hazim Ali Hussein, Laith A. Younus, Fadhil A. Nasser, Hasanain A. A. Almohseni. Effect of Epigallocatechin‐3‐Gallate on Depression‐Related Cytokines in Thalassemia Patients: Molecular and Cellular Evaluation. Journal of Clinical Laboratory Analysis 2026; 40(4) doi: 10.1002/jcla.70171
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| 2 |
Jiaojiao Shu, Xin Xie, Sixi Wang, Zuochen Du, Pei Huang, Yan Chen, Zhixu He. CRISPR/Cas-edited iPSCs and mesenchymal stem cells: a concise review of their potential in thalassemia therapy. Frontiers in Cell and Developmental Biology 2025; 13 doi: 10.3389/fcell.2025.1595897
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| 3 |
Aibek Mirrakhimov. Internal Medicine Basics for Anesthesiology. 2026; doi: 10.1007/978-3-032-29397-8_68
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| 4 |
Aikaterini Poulaki, Sophia Delicou. Unstable Hemoglobin Variants: Molecular Mechanisms, Clinical Phenotypes, and a Practical Diagnostic and Management Approach. Hemoglobin 2026; 50(4) doi: 10.1080/03630269.2026.2674946
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| 5 |
Brena André Rodrigues da Silva, André Cavichioli Brito . APLICAÇÕES DE CRISPR-CAS9 NA CORREÇÃO DA MUTAÇÃO DA TALASSEMIA BETA: AVANÇOS TECNOLÓGICOS, DESAFIOS TRANSLACIONAIS E PERSPECTIVAS FUTURAS. Revista Multidisciplinar do Nordeste Mineiro 2025; 20(2) doi: 10.61164/ef6z6361
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| 6 |
Hassan Saeed, Nageen Hussain, Tariq Aziz, Nawal Al-Hoshani, Omniah A. Mansouri, Mariam Abdulaziz Alkhateeb. In Silico Pharmacological Evaluation of Azadirachta indica Phytochemicals Targeting Thalassemia-Associated Genes and Proteins. Journal of Computational Biophysics and Chemistry 2026; 25(11) doi: 10.1142/S2737416526500407
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| 7 |
Murtadha A. AL-Mudhafar, Ismael Raheem Al‐Muhana, Hussein Ali Kadhum, Israa Ketab Alyasiri. Iron Overload–Linked Immunometabolic Dysregulation and John Cunningham Virus Seropositivity in Children with β-Thalassemia Major and Intermedia. International Journal of Medical Parasitology and Epidemiology Sciences 2026; 7(3) doi: 10.34172/ijmpes.6286
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| 8 |
Rajkumar Motiram Meshram, Sagar Chopde, Ashma Rashid. Subclinical cardiac dysfunction in transfusion-dependent beta-thalassemia children, an experience from central India: A comparative cross-sectional study. Annals of Pediatric Cardiology 2026; 19(5) doi: 10.4103/apc.apc_126_26
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| 9 |
Christos Savvidis, Ioannis Ilias. Endocrine dysfunction in homozygous beta-thalassemia: An underrecognized and undertreated consequence of prolonged survival. World Journal of Clinical Cases 2025; 13(24): 107612 doi: 10.12998/wjcc.v13.i24.107612
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| 10 |
Julien Guy, Marie‐C Béné, Ramon Simon Lopez, Marc Maynadié, Céline Row. Automated Morphologic Differentiation Between Iron Deficiency Anemia and Thalassemia. Journal of Clinical Laboratory Analysis 2025; 39(19) doi: 10.1002/jcla.70097
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| 11 |
Abdelrahman A. Abdelrahman, Randa M. Talaat, Ibrahim Abdo El-Halfawy, Mohamed Ramzy Alalwi, Dina Malak Yousef Rizk. Genetic polymorphism of SNPs rs9399137 and rs4895441in HBS1L-MYB and SNP rs766432 in BCL11A among β-thalassemia Egyptian patients. BMC Genomic Data 2026; 27(1) doi: 10.1186/s12863-026-01436-4
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| 12 |
Helle Pilgaard Kristiansen, Jesper Petersen, Peter Schou, Peter H. Nissen, Anne Winther-Larsen. A novel 17.9 kb deletion of the beta-globin gene causing beta-thalassemia trait in a Danish male. Clinical Biochemistry 2025; 140 doi: 10.1016/j.clinbiochem.2025.111035
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| 13 |
Jing Guo, Teng Li, Liang Liang, Jialiang Huang, Youqiong Li. Prenatal Counseling Conundrum: Unexpectedly Mild Phenotype in a Pregnant Woman with Homozygous CD41/42(-TTCT) β-Thalassemia. Hemoglobin 2026; 50(3) doi: 10.1080/03630269.2026.2664191
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