Results 91 to 100 of about 694,655 (127)
ASSOCIATION BETWEEN THALASSEMIA TRAIT AND INSULIN RESISTANCE
, 2018 Introduction: One of the subjects discussed in the patients with thalassemia major and thalassemia intermedia is whether excess iron deposition in the liver causes insulin resistance or not.
Isiklar, A., Karsidag, K.
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Molecular Genetics &Genomic Medicine, Volume 14, Issue 11, November 2026.β‐Thalassemia intermedia exhibits distinct region‐specific molecular patterns shaped by three interacting genetic axes: β‐globin mutation severity, HbF‐inducing modifiers, and α‐globin gene dosage. Mediterranean populations are predominantly mutation‐driven, Middle Eastern populations rely on HbF compensation, and Asian populations are governed by ...
Kavindya Fernando +2 more
wiley +1 more source
, 2011 Thalassemia is a congenital hemolytic disorder caused by a partial or complete deficiency of α- or β-globin chain synthesis. It has been seen that thalassemic patients exhibit an increased frequency of thrombotic events.
G. Checcucci, M. Galeano, M. Ceruso
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Causes of New Cases of Major Thalassemia in Sistan and Balouchistan Province in South-East of Iran
Iranian Journal of Public Health, 2012 Background: Thalassemia is the most common monogenic disease in South-East of Iran. Despite the 70% reduction in Iranian thalassemia cases after thalassemia control comprehensive program, 601 affected babies were born in Sistan and Balouchistan Province,
S Izadi +3 more
doaj +2 more sources
Bioscientific Review, 2023 Objective The objective of this study was to study relation of ß-thalassemia and its types (major, minor, intermedia) with ABO and Rh blood groups in Lahore, Pakistan.
Kainat Waheed +2 more
doaj
Relationship between Bipolar I disorder and β thalassemia minor [PDF]
, 2005 Background and purpose: Previous studies indicate an important genetic factor in the etiology of β-Thalassemia and bipolar mood disorder. There has been several case reports implicating a possible association between the two conditions.
V. Ghaffari +3 more
core
, 2015 Thalassemia is a hereditary hemolytic anemia which is inherited from the parents to their children resessively caused by globin gene mutation.
Hidayat
core
, 2018 Objective and importance: To verify the presence of β-thalassemia in subjects showing hematologic phenotype of α-thalassemia, conduct normal molecular sequence analysis of the α-globin genes, and detect the absence of the most frequent α-thalassemia ...
Clelia Scarano (2879918) +5 more
core +1 more source
Iraqi Journal of Pharmaceutical Sciences, 2017 A representative sample of a thousand volunteer university students was screened for evidence of thalassemia minor.Complete blood counts using automated blood cell analysers and blood smears were examined.
Abdulkadir A. Alnakshabandi +1 more
doaj