Results 131 to 140 of about 4,949,451 (244)

Lack of awareness about thalassemia; a social factor in the propagation of beta thalassemia gene in Pakistan: A population study

Mediterranean Journal of Hematology and Infectious Diseases, 2014
Background: Beta thalassemia is the most common genetic disorder in Pakistan. Thalassemia is a preventive disease a fact well demonstrated by countries such as Italy, Greece and Cyprus.
Muhammad Usman
doaj  

Evalution of HbA2 In Minor β Thalassemia Carriers Reffered to Kerman Special Disease Center [PDF]

Journal of Kerman University of Medical Sciences, 2003
Increased HbA2 is a characteristic finding in minor beta thalassemia. Minor β-thalassemia is a heterozygote form of β-thalassemia that carries thalassemia genes but does not cause thalassemia disease.
M Atapour, AR Zohoor, A Zolala, AR Arjmand   +3 more
doaj  

Optimising Haematopoietic Stem Cell Transplantation: Enhancing Myeloablation Sensitivity and Alleviating Anaemia Using Roxadustat (FG‐4592)

Cell Proliferation, Volume 59, Issue 11, November 2026.
The use of FG‐4592 in the process of myeloablation can promote haematopoietic cell apoptosis for more effective myeloablation, maintain the number of RBC and may create a pluripotent microenvironment suitable for donor cells, so as to enable more effective haematopoietic reconstruction of donor cells in vivo.
Guanheng Yang, Jiahui Wu, Xinbing Guo, Wenchen Shen, Xiao Sang, Xiuli Gong, Shu‐Zhen Huang, Jingzhi Zhang, Fanyi Zeng   +8 more
wiley   +1 more source

Hubungan Gambaran Dermatoglifi dengan Penyakit β – Thalassemia Major [PDF]

, 2017
Latar Belakang : β – Thalassemia Major adalah salah satu jenis penyakit Thalassemia yang paling berat. Anak dengan β – Thalassemia Major harus segera dikenali dan diberi penanganan untuk menghindari prognosis yang semakin buruk.
A, NISA`U LUTHFI NUR
core  

B-thalassemia major

Saudi Medical Journal, 2003
Zakaria M, Al-Hawsawi, Ghousia A, Ismail, Hanan A, Al-Harbi, Zaki R, Al-Sobhi   +3 more
openaire   +2 more sources

Endocrinopathies in Turkish Children with Thalassemia Major

, 2017
Aim: Endocrinopathies are common in patients with thalassemia major (TM) and affect their life quality. Our aim was to identify the frequency of growth retardation and endocrine complications in these patients.
Belma Haliloğlu, Funda Tayfun, Gülen Tüysüz   +2 more
core   +1 more source

Serum lipid profiles in patients with beta-thalassemia major and intermedia in southern Iran

, 2010
BACKGROUND: Beta-thalassemia is considered to be the most frequent hereditary blood disorder worldwide. Lipid abnormalities have been detected in different types of beta-thalassemia.
Behrang Samadi, Mehran Karimi, Sezaneh Haghpanah, Afsaneh Ashrafi, Maryam Davani   +4 more
core  

Genotype–phenotype correlation among beta-thalassemia and beta-thalassemia/HbE disease in Thai children: predictable clinical spectrum using genotypic analysis

, 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, Boonyawat B, Traivaree C, Monsereenusorn C, Prasertsin W   +4 more
core  

Electrocardiographic changes among beta-thalassemic major patients in ibn al-baladi thalassemia center-Baghdad

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, FarisH. Al-Lami, Mousa Qasim Hussein   +2 more
doaj  

Osteoporosis in thalassemia major: A possible role of chelation therapy

, 1999
Bone metabolism and turnoveris influenced by different factors in thalassemia major patients. It is observed a role od chelating agents in the pathogenesis of osteopenia and osteoporosis in thalassemia major ...
Iolascon, G, De Rosa, C, Danesi, L, Imonti, F, Cappellini, MD, Siciliano, MC, Iolascon, A, Schettini, F, Perrotta, S   +8 more
core