Results 281 to 290 of about 1,048,085 (335)
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Accelerated atherosclerosis in beta-thalassemia
American Journal of Physiology-Heart and Circulatory Physiology, 2023This work definitively shows for the first time that beta-thalassemia leads to accelerated atherosclerosis. We demonstrated that intravascular hemolysis is a prominent feature in beta-thalassemia and the resulting increases in free heme are mechanistically relevant.
Julian Hurtado +8 more
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Beta-thalassemia Intermedia: An Overview
Pediatric Annals, 2008CME Educational Objectives 1. Review the metabolic pathways critical to maintaining red cell membrane integrity. 2. Produce a classification scheme
F. El Rassi +3 more
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β-Thalassemia Mutations in Corsica
Hemoglobin, 2000Screening of beta thalassemia mutations in Corsica.
Varesi L +4 more
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Hypertriglyceridemia in homozygous beta thalassemia
The Journal of Pediatrics, 1975A case of hypertriglyceridemia in association with homozygous beta-thalassemia in an 11-month-old female infant is reported. The hypertriglyceridemia proved to be secondary, as it was indicated by clinical features as well as laboratory findings. Attention is called to a possible alteration of lipid metabolism in association with thalassemia major.
M R, Ameri +3 more
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C3 Polymorphism in Beta-Thalassemia
Acta Haematologica, 1984The distribution of phenotypes and gene frequencies of the third component of complement (C3) were studied in 106 beta-thalassemic patients and in 112 carriers of the beta-thalassemia trait. A statistically significant association was found between the C3F gene and homozygous beta-thalassemia.
A, Germenis +4 more
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Ophthalmic Evaluation in Beta-Thalassemia
The Indian Journal of Pediatrics, 2017To determine the association of ocular manifestations in beta-thalassemia with the patient's age, blood transfusion requirements, average serum ferritin and dose and duration of iron chelation therapy.Sixty multi-transfused beta thalassemia patients of 12 to 18 y of age on chelation therapy were included in this cross-sectional analysis. Structural and
Rashid H, Merchant +3 more
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Gene addition for beta thalassemia
Annals of the New York Academy of Sciences, 2023AbstractIndividuals with transfusion‐dependent beta thalassemia require a high burden of care and experience significant morbidity from the underlying disease and its treatment, which negatively impact the quality of life. Allogeneic hematopoietic stem cell transplantation offers the chance for a cure, but donor availability and transplant‐related ...
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Pycnodysostosis with heterozygous beta-thalassemia
Pediatric Radiology, 1977A 6-year follow-up of a Greek girl with pycnodysostosis associated with heterozygous beta-thalassemia is reported. Active rickets in infancy was superimposed on pycnodysostosis. In the family the autosomal recessive disease, pycnodysostosis, appeared in two of three siblings in combination with the autosomal dominant disease, thalassemia minor.
G, Benz, E, Schmid-Rüter
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Musculoskeletal imaging manifestations of beta-thalassemia
Skeletal Radiology, 2021Maryam Hajimoradi +3 more
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Neurological complications of beta-thalassemia
Annals of Hematology, 2015The thalassemias are the most common single gene disorder in the world. Over the last years, several reports have demonstrated neurological complications in beta-thalassemia patients. In most cases, these complications remained subclinical and were detected only during neuropsychological, neurophysiological, or neuroimaging evaluation.
P. Nemtsas +4 more
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