Results 211 to 220 of about 607,752 (259)

Beta Thalassemia Major

Gomal Journal of Medical Sciences, 2007
Muhammad Asghar
doaj  

Beta-thalassemia Intermedia: An Overview

Pediatric Annals, 2008
CME Educational Objectives 1. Review the metabolic pathways critical to maintaining red cell membrane integrity. 2. Produce a classification scheme
F. El Rassi, M.D. Cappellini, A. Inati, A. Taher   +3 more
openaire   +4 more sources

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Beta Thalassemia

Hematology/Oncology Clinics of North America, 2019
Eugene Khandros, Janet L Kwiatkowski
exaly   +2 more sources

Accelerated atherosclerosis in beta-thalassemia

American Journal of Physiology-Heart and Circulatory Physiology, 2023
This 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, Hassan Sellak, Giji Joseph, Caitlin V. Lewis, Crystal R. Naudin, Sergio Garcia, James Robert Wodicka, David R. Archer, W. Robert Taylor   +8 more
openaire   +2 more sources

Hypertriglyceridemia in homozygous beta thalassemia

The Journal of Pediatrics, 1975
A 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, M, Alebouyeh, M, Ziai, R B, Conn   +3 more
openaire   +2 more sources

Neurological complications of beta-thalassemia

Annals of Hematology, 2015
The 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, M. Arnaoutoglou, V. Perifanis, E. Koutsouraki, A. Orologas   +4 more
openaire   +2 more sources

Gene addition for beta thalassemia

Annals of the New York Academy of Sciences, 2023
Abstract Individuals 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.
openaire   +2 more sources

Pycnodysostosis with heterozygous beta-thalassemia

Pediatric Radiology, 1977
A 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
openaire   +2 more sources

C3 Polymorphism in Beta-Thalassemia

Acta Haematologica, 2009
The distribution of phenotypes and gene frequencies of the third component of complement (C3) were studied in 106 β-thalassemic patients and in 112 carriers of the β-thalassemia trait. A statistically significant association was found between the C3F gene and homozygous β-thalassemia.
A, Germenis, M, Kalantzi, A, Karamerou, C, Politi, A, Fertakis   +4 more
openaire   +2 more sources