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Frequency of Cholelithiasis in Patients With Beta-Thalassemia Intermedia With and Without Hydroxyurea
Beta Thalassemia Intermedia Cholelithiasis Hydroxyurea
2015/10/13
Background: Recent studies regarding the effect of hydroxyurea (HU) in thalassemia have revealed favorable effects on the reduction of ineffective erythropoiesis.
Comparison between Deferoxamine and Combined Therapy with Deferoxamine and Deferiprone in Iron Overloaded Thalassemia Patients
Thalassemia major Deferoxamine Deferiprone Chelation therapy
2015/9/21
Background: Iron overload is the main cause of morbidity and mortality in patients with beta thalassemia major. Effective and convenient iron chelation remains one of the main targets of clinical mana...
Identification of a Novel Frameshift Mutation [Codon 3 (+T)] in a Turkish Patient with b-Thalassemia Intermedia
b-thalassemia b-globin gene insertion frameshift mutation DNA sequencing
2009/6/22
b-Thalassemia, one of the most widespread genetic diseases in the world, is an autosomal recessive disease generally caused by point mutations in the b-globin gene that is located as a cluster on the ...
Beta thalassemia major, a cause of testicular microlithiasis
Testicular microlithiasis Beta thalassemia Malignant precursor Scrotal ultrasound
2015/9/9
Testicular microlithiasis is a rare condition characterized by deposition of calcium in the Lamina of semineferous tubules of testis. The ultrasound of testicular microlithiasis shows bright 1-3 mm ec...
β-Globin Gene Cluster Haplotypes in Iranian Patients with β-Thalassemia
β-globin gene haplotypes thalassemia Iran
2010/4/2
Introduction: β-globin gene cluster haplotypes are useful in diagnosis of particular molecular defects in β-thalassemia, prenatal diagnosis of β-thalassemia, and elucidating population affinities. Met...