Results 101 to 110 of about 722,667 (218)
The Primary Reasons People Participate in Maternal‐Fetal Phase I Clinical Trials Are Psychosocial
Ethics &Human Research, Volume 48, Issue 6, Page 20-31, November–December 2026.ABSTRACT Recent critiques of ethical guidance for maternal‐fetal therapy clinical trials has highlighted the need to weigh maternal, fetal, and societal interests, respectively, while deprioritizing psychosocial reasons for participation. Psychosocial reasons refer to the psychological and social influences on study participants’ decisions, and they ...
Julia E. H. Brown +6 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
core +1 more source
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