Results 131 to 140 of about 71,330 (251)
Lived experiences of Iranian parents of beta-thalassemia children [PDF]
, 2017 Aziz Shahraki-vahed,1 Mohammadreza Firouzkouhi,1 Abdolghani Abdollahimohammad,1 Jamile Ghalgaie2 1Department of Medical Surgical, Faculty of Nursing and Midwifery, Zabol University of Medical Science, Zabol, Iran; 2Emam Khomeni Hospital, Zabol University
Shahraki-vahed A +3 more
core
Journal of Child Psychology and Psychiatry, Volume 67, Issue 8, Page 1404-1411, August 2026.Background Attention‐deficit/hyperactivity disorder (ADHD) is a chronic neurodevelopmental disorder marked by persistent patterns of inattention, disorganization, hyperactivity, and impulsivity. Increasing evidence implicates immune‐inflammatory processes in its etiology, with observed associations between ADHD and infectious diseases, allergic ...
Eugene Merzon +11 more
wiley +1 more source
Antioxidant Effects of CoQ10 in Transfusion-Dependent β-Thalassemia Major Patients: Implications for Ferroptosis-Related Pathways [PDF]
Kiavash Fekri,1 Mohammad Mehdi Mirforoughi,2 Yaser Salehinajafabadi,3 Hadi Raeisi Shahraki,4 Raziyeh Ershadi,5 Shima Rahmati1 1Cancer Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran; 2Shahid Beheshti University of Medical ...
Ershadi R +5 more
core
Genotype–phenotype correlation among beta-thalassemia and beta-thalassemia/HbE disease in Thai children: predictable clinical spectrum using genotypic analysis [PDF]
, 2018 Chanchai Traivaree,1 Chalinee Monsereenusorn,1 Piya Rujkijyanont,1 Warakorn Prasertsin,2 Boonchai Boonyawat3 1Division of Hematology/Oncology, Department of Pediatrics, Phramongkutklao Hospital and College of Medicine, Bangkok, Thailand; 2Department of ...
Rujkijyanont P +4 more
core
Redefining the role of the transfusion medicine physician in the era of advanced cellular therapies
Transfusion, EarlyView.
Eric A. Gehrie, Kevin J. Land
wiley +1 more source
Beta Thalassemia Major Bone Marrow Transplant [PDF]
Bone Marrow Transplant is the only possible cure till now for the genetic disorder thalassemia. Thalassemia Major can be managed by regular blood transfusions and iron chelation, but the quality of life is still poor and individuals suffering from this ...
Anand, Ayush
core +1 more source
Prevalence of hypoparathyroidism in patients with thalassemia major in Iran [PDF]
, 2016 BACKGROUND AND OBJECTIVE: Hypoparathyroidism is one the common complications of endocrine in patients with thalassemia major. Several studies have been conducted to report the prevalence of Hypoparathyroidism in patients with thalassemia major in Iran ...
Azami, M., Sayehmiri, K., Rahmati, S.
core
Dermatoglyphs in Patients with Beta-Thalassemia Major and Their Thalassemia Carrier Parents [PDF]
, 2009 Dermatoglyphs are cutaneous ridges on the fingers, palms, and soles, formed during early intrauterine life. During this period, and only then, genetic and environmental factors can influence their formation.
Savas, Nazan +5 more
core +1 more source
مجله كليه طب الكندي, 2013 Background :Thalassemia is an autosomal disease of the haemoglobin. Two types of thalassemia are recognized: thalassemia major and thalassemia intermedia.
Suhad Jassim Mohammed +2 more
doaj
Breathless: Beta Thalassemia Major
The American Journal of Medicine, 2017 Vassiliki Katsi +3 more
openaire +3 more sources