Results 161 to 170 of about 2,697,911 (252)

‘Phenoconversion’ in adult patients with β‐thalassemia

: Rate and risk factors for phenoconversion from non-transfusion-dependent β-thalassemia (NTDT) to transfusion-dependent β-thalassemia (TDT) during a 10-year follow up of adult patients in ...
Barella, Susanna, Lisi, Roberto, Pasanisi, Annamaria, Lucia De Franceschi, Domenico Roberti, Martina Culcasi, Ferrero, Giovanni Battista, Gianesin, Barbara, Musallam, Khaled M., Origa, Raffaella, Valeria Pinto, Longo, Filomena, Forni, Gian Luca, Roberta Sciortino   +13 more
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Frequency of heart complication in beta thalassemia major children at tertiary care hospital

Journal of Contemporary Pharmacy
Objective: to evaluate the prevalence of cardiac problems, including myocardial iron deposition, pericarditis, and valvular abnormalities, among people with β-thalassemia and to shed light on the distribution of β-thalassemia and hemoglobin levels ...
Ammad Ali, Shoaib, Hanadi Shad, Jehanzeb Khan, Abdur Rehman, Arooj Khan, Shaista Azeem Khan, Shams ul Arifeen   +7 more
doaj   +2 more sources

A particular focus on the prevalence of α-thalassemia and β-thalassemia among pregnant women in Changsha County, Hunan Province [PDF]

BackgroundThalassemia is a inherited monogenic blood disorder and more prevalent in southern China. In this study, Our aim was to elucidate the molecular spectrum and phenotypic features of thalassemia in pregnant women in Changsha County.MethodsNext ...
Yu Xia, Yang Lu, Meng Zhang, Mudan Yang, Cailian Huang   +4 more
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HUBUNGAN GAMBARAN DERMATOGLIFI DENGAN PENYAKIT β - THALASSEMIA MAJOR [PDF]

, 2015
Nisa’u Luthfi Nur Azizah, G0011151, 2015. Hubungan Gambaran Dermatoglifi dengan Penyakit β – Thalassemia Major. Skripsi Fakultas Kedokteran Universitas Sebelas Maret Surakarta.
Azizah, Nisa'u Luthfi Nur
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Analysis of thalassemia genotypes and HbA2 test results in pregnant women in Shenzhen, China

Scientific Reports
To examine the thalassemia genotypes and distribution among pregnant women in Shenzhen, as well as the diagnostic value of HbA2 in thalassemia screening, in order to provide scientific evidence for thalassemia prevention and control in this region.
Hou Qian, Weihua Zhao, Weifeng Li, Yike Wu, Xiuhua Lin, Jianlin Huang, Hong Zhang, Dayong Gu   +7 more
doaj   +1 more source

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, M. Zarghami, A. Saljughian, H. Hoseini   +3 more
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The molecular basis of β-thalassemia.

, 2013
The β-thalassemias are characterized by a quantitative deficiency of β-globin chains underlaid by a striking heterogeneity of molecular defects. Although most of the molecular lesions involve the structural β gene directly, some down-regulate the gene ...
Thein, Swee Lay
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Laboratory and paraclinical information of diabetic β-thalassemia patients.

Laboratory and paraclinical information of diabetic β-thalassemia patients.
Aily Aliasgharian (17781495), Hossein Karami (10119113), Amir Mosanejad-Galchali (17781492), Mehrnoush Kosaryan (17781489), Mohammad Naderisorki (11395283), Hasan Karami (17781498), Hadi Darvishi-Khezri (10119110), Mobin Ghazaiean (14440743)   +7 more
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Molecular and hematological characterization of thalassemia and hemoglobinopathies among pediatric patients in northern Lao People’s Democratic Republic

Scientific Reports
Thalassemia and hemoglobinopathies are highly prevalent in the Lao People’s Democratic Republic (Lao PDR). Luang Prabang Province represents an ethnically diverse area with a high burden of pediatric anemia, but the molecular and hematological ...
Volapheth Kanyasone, Pichpimon Pakpuak, Supitsaraporn Satewin, Anupong Pansuwan, Kritsada Singha, Attawut Chaibunruang, Hataichanok Srivorakun, Supan Fucharoen, Annkham Thammaseng, Sengmany Sengphachan, Hame Thiphalack, Anousine Phonedala, Supawadee Yamsri   +12 more
doaj   +1 more source

The multicenter THALAMOSS cellular Biobank for β-Thalassemia

, 2016
The production and validation of a cellular thalassemia Biobank was conducted within the multicenter European Project THALAMOSS (THalassemia MOdular Stratification System for personalized therapy of β-thalassemia).
Menzel, Stephan, Moi, Paolo, Kleanthous, Marina, LAMPRONTI, Ilaria, Thein, Swee Lay, GAMBARI, Roberto, ZUCCATO, Cristina, Lederer, Carsten, COSENZA, Lucia Carmela, de Martis, Franca Rosa, FINOTTI, Alessia, BREDA, Laura, BREVEGLIERI, Giulia, Rivella, Stefano, Satta, Stefania, Breton, Amandine, BIANCHI, Nicoletta, Manunza, Laura, BORGATTI, Monica   +18 more
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