Results 181 to 190 of about 1,051,766 (308)
Hearing Loss in Beta-Thalassemia: Systematic Review [PDF]
, 2021 Immacolata Tartaglione +6 more
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British Journal of Haematology, Volume 208, Issue 1, Page 348-352, January 2026.In this post hoc analysis of the phase 2 BEYOND trial, the majority of patients with non‐transfusion‐dependent β‐thalassaemia achieved clinically meaningful haemoglobin levels ≥10.0 g/dL and increases from baseline ≥1.0 g/dL, thresholds associated with reduced risk of morbidity and mortality and recommended as an indication and target for treatment by ...
Khaled M. Musallam +11 more
wiley +1 more source
Clinical and Translational Science, Volume 19, Issue 1, January 2026.ABSTRACT Maternal cell contamination (MCC) in fetal specimens poses a major risk for misdiagnosis in prenatal genetic testing. Standard variable number tandem repeat (VNTR) analysis of the thyroid peroxidase (TPO) gene intron 10 is informative for MCC detection but traditionally requires DNA extraction, limiting its use in resource‐limited laboratories.
Phongsathorn Wichian +5 more
wiley +1 more source
Iron‐related intercellular communication in the liver: Main players and mechanisms
European Journal of Clinical Investigation, Volume 56, Issue 1, January 2026.Iron exchange between liver cell types is vital for organism health, yet its mechanisms remain poorly understood. In this review, we address intercellular communication governing hepatic iron regulation across different liver diseases. We summarize recent insights into how hepatocytes, macrophages, endothelial and stellate cells coordinate iron storage,
Óscar Fonseca +4 more
wiley +1 more source
Detection of Rare Thalassemia Variants Using Accurate Circular Consensus Long‐Read Sequencing
Human Mutation, Volume 2026, Issue 1, 2026.Objective The aim of this study is to evaluate the efficacy of accurate circular consensus long‐read sequencing in the detection of rare thalassemia. Methods Conventional molecular analysis on globin genes has limitations because of the broad spectrum of genetic variants, complex genetics, and genotype–phenotype correlation. Accurate circular consensus
Xiaoqiang Zhou +10 more
wiley +1 more source
Journal of Tehran University Heart Center, 2015 Background: Heart disease is the main cause of mortality and morbidity in patients with beta thalassemia, rendering its early diagnosis vital. We studied and compared echocardiographic findings in patients with beta thalassemia major, patients with beta ...
Noormohammad Noori +5 more
doaj
Globin Chain Synthesis in the Marrow and Reticulocytes of Beta Thalassemia, Hemoglobin H Disease, and Beta Delta Thalassemia [PDF]
, 1972 Mordechai Shchory, Bracha Ramot
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Hypogonadism in Female Patients with Beta Thalassemia Major
, 2018 Alice Albu, Dragoș Albu
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Serum erythropoietin and erythropoiesis in high- and low-fetal hemoglobin beta-thalassemia intermedia patients [PDF]
, 1994 R. Galanello +8 more
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