[HTML][HTML] A systematic review and meta-analysis of stature growth complications in β-thalassemia major patients

M Arab-Zozani, S Kheyrandish, A Rastgar… - Annals of global …, 2021 - ncbi.nlm.nih.gov
Background: Blood transfusion is a traditional treatment for β-thalassemia (β-thal) that
improves the patients' anemia and lifespan, but it may lead to iron overload in parenchymal …

Elevated Prevalence of Abnormal Glucose Metabolism and Other Endocrine Disorders in Patients with β‐Thalassemia Major: A Meta‐Analysis

LN He, W Chen, Y Yang, YJ Xie… - BioMed research …, 2019 - Wiley Online Library
Background. Endocrinopathies are common in patients with β‐thalassemia major despite
parenteral iron chelation therapy with deferoxamine. Prevalence of abnormal glucose …

Body composition in adult patients with thalassemia major

M Vlychou, E Alexiou, P Thriskos… - International Journal …, 2016 - Wiley Online Library
Objective. To assess body composition in adult male and female patients with thalassemia
major by dual‐energy X‐ray absorptiometry (DXA) and to compare the findings with a group …

The role of using different reference population in the prevalence of low BMD in the thalassemia patients

MR Mohajeri-Tehrani, N Darvishian, F Arab… - Journal of Diabetes & …, 2020 - Springer
Purpose Prevalence of osteoporosis reported as high as 50% in thalassemia major patients.
We compared bone density (BMD) of our patients with results of bone densitometry of …

[HTML][HTML] How Age, Sex and Transfusion Affects the Incidence of Endocrine and Bone Density Disorders in Major Thalassemic Patients

MR Mohajeri-Tehrani, SA Alemzadeh… - Iranian Journal of …, 2024 - ncbi.nlm.nih.gov
Background: Beta-thalassemia major patients frequently have endocrinopathies. We tried to
determine relation between demographic and transfusion factor and endocrinopathies …

Investigating β Thalassemia Patients and Their Growth: A Brief Review and Our Clinical Experience

MR Mohajeri-Tehrani, F Arab, S Salemkar… - Journal of Pediatrics …, 2024 - jpr.mazums.ac.ir
Background: The prevalence of short stature was reported high in thalassemia major
patients. It causes mental and social problems for them. As different cut-off points for growth …

[HTML][HTML] Bone density changes in thalassaemic patients with age and time period

F Mohseni, M Mohajeri-Tehrani, B Larijani, Z Hamidi - HK J Paediatr, 2016 - hkjpaed.org
Purpose: Chronological and longitudinal changes of bone density in patients with secondary
osteoporosis, have been shown helpful in providing a model of calcium and bone …

Short-term Assessment of HSCT Effects on the HypothalamusPituitary Axis in Pediatric Thalassemic Patients

AA Hamidieh, F Mohseni, M Behfar… - Archives of Iranian …, 2018 - journalaim.com
Background: Beta thalassemia major (BTM) and its treatment by hematopoietic stem cell
transplantation (HSCT) may have deleterious effects on the endocrine systems. We …

[PDF][PDF] Διερεύνηση της οστικής πυκνότητας, της σύστασης μάζας σώματος και των δεικτών του οστικού μεταβολισμού σε ελληνικό πληθυσμό με ομόζυγη μεσογειακή …

ΕΓ Αλεξίου - 2021 - ir.lib.uth.gr
Περίληψη Οι ασθενείς με θαλασσαιμία εμφανίζουν μια πολυπαραγοντική διαταραχή των
οστών με προεξάρχουσα αιτία την υπερπλασία του ερυθρού μυελού που καταλαμβάνει τις …

Glycated Albumin Sebagai Deteksi Awal Hiperglikemia pada Anak Thallassemia Mayor Usia 9-18 Tahun di RSUD Dr. Moewardi

D Candrarukmi - 2020 - digilib.uns.ac.id
Puji syukur Penulis sampaikan kepada Allah Subhanahu wa Ta'alaa atas rahmat dan
karuniaNya sehingga karya tulis akhir dengan judul “Glycated albumin sebagai deteksi awal …