Results 111 to 120 of about 840,950 (218)

Molecular characterization of thalassemia intermedia in Indians

Haematologica, 2006
Thalassemia intermedia shows considerable heterogeneity. The purpose of this study was to evaluate the prevalence and effect of common molecular determinants in thalassemia intermedia.
I Panigrahi, S Agarwal, M Pradhan, DR Choudhry, VP Choudhry, R Saxena   +5 more
doaj  

Serum lipid profiles in patients with beta-thalassemia major and intermedia in southern Iran

, 2010
BACKGROUND: Beta-thalassemia is considered to be the most frequent hereditary blood disorder worldwide. Lipid abnormalities have been detected in different types of beta-thalassemia.
Behrang Samadi, Mehran Karimi, Sezaneh Haghpanah, Afsaneh Ashrafi, Maryam Davani   +4 more
core  

Pre-Natal Diagnosis of beta – Thalassemia by Chorionic Villous Sampling

Journal of Rawalpindi Medical College, 2009
Background: To promote the utility of Chorionic Villous Sampling (CVS) for pre-natal diagnosis of beta thalassemia in at risk population and to highlight its demographic area distribution and effect of consanguinity.
Shazia Syed,
doaj  

BETA-THALASSEMIA

International Research Journal of Modernization in Engineering Technology and Science, 2023
openaire   +1 more source

Molecular identification of Sicilian (8 beta)degrees-thalassemia associated with beta-thalassemia and hemoglobin S in Brazil

, 2015
We describe the clinical and molecular characteristics of two unrelated Brazilian families with an association of the Sicilian form of (deltabeta)degrees-thalassemia with hemoglobin S and beta-thalassemia. Direct sequencing of the beta-globin gene showed
de Andrade, TG, Sonati, MF, Saad, STO, Fattori, A, Costa, FF   +4 more
core  

Molecular Identification Of Sicilian (deltabeta) Degrees-thalassemia Associated With Beta-thalassemia And Hemoglobin S In Brazil.

, 2015
We describe the clinical and molecular characteristics of two unrelated Brazilian families with an association of the Sicilian form of (deltabeta) degrees -thalassemia with hemoglobin S and beta-thalassemia.
Costa, F F, Sonati, M F, de Andrade, T G, Fattori, A, Saad, S T O   +4 more
core  

Arterial calcifications in beta-thalassemia

, 1998
The purpose of this study was to define the incidence of arterial calcifications in patients with beta-Thalassemia. beta-thalassemia patients have been shown to present a high prevalence of angioid streaks and skin lesions characteristic of ...
Kavouklis, E, Tsironi, M, Aessopos, A, Samarkos, M, Papaioannou, D, Stamatelos, G, Vaiopoulos, G, Voskaridou, E, Loukopoulos, D   +8 more
core  

Analysis of various electrocardiographic and echocardiographic parameters in beta thalassemia patients with iron overload. [PDF]

Ann Pediatr Cardiol
Girija H, Sridhar A, Muthukumaran CS, Ramkishore S, Ganesan R, Mahitha V, Arun V.   +6 more
europepmc   +1 more source

Treatment Options for Beta-Thalassemia

Beta-thalassemia, a hereditary blood disorder caused by point mutations affecting beta-globin synthesis, impairs erythrocyte oxygen transport. Due to its resistance, beta-thalassemia originally propagated in regions with high malaria prevalence.
Ainsley R Hartman, Vincent S Gallicchio
core   +1 more source

Ocular Complications in Patients With Transfusion-Dependent Beta-Thalassemia Receiving Deferasirox: A Cross-Sectional Study. [PDF]

Health Sci Rep
Medghalchi A, Kanafi AR, Alizadeh Y, Baghersalimi A, Doorandish M, Hassanzadeh Rad A, Kianmehr S, Darbandi B.   +7 more
europepmc   +1 more source