Works matching Thalassemia
Results: 5000
Biochemical and Genetic Study in Blood of β– Thalassaemia Children in Mosul City, Iraq.
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- Iraqi Journal of Science, 2021, v. 62, n. 8, p. 2501, doi. 10.24996/ijs.2021.62.8.2
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- Article
Molecular Understanding of Non-Transfusion-Dependent Thalassemia Associated with Hemoglobin E-β-Thalassemia in Northeast Thailand.
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- Acta Haematologica, 2016, v. 136, n. 4, p. 233, doi. 10.1159/000449120
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- Article
Erythrocyte indices in a large cohort of β‐thalassemia carrier: Implication for population screening in an area with high prevalence and heterogeneity of thalassemia.
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- International Journal of Laboratory Hematology, 2019, v. 41, n. 4, p. 513, doi. 10.1111/ijlh.13035
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- Article
COVID-19 in Patients with Transfusion Dependent Thalassemia (TDT) in Indonesia: Characteristics of the Disease and Patients, and Comparison between Epidemiological Data for COVID-19 and Thalassemia in Indonesia and Southeast Asia.
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- Hematology Reports, 2022, v. 14, n. 1, p. 2, doi. 10.3390/hematolrep14010002
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- Article
RESTLESS LEG SYNDROME IN ADULT PATIENTS WITH β-THALASSEMIA MAJOR .
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- Clinical Neuroscience / Ideggyógyászati Szemle, 2021, v. 74, n. 7/8, p. 266, doi. 10.18071/isz.74.0266
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- Article
Alpha thalassemia deletions found in suspected cases of beta thalassemia major in Pakistani population.
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- Pakistan Journal of Medical Sciences, 2017, v. 33, n. 2, p. 411, doi. 10.12669/pjms.332.11834
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- Article
IMPACT OF COINHERITANCE OF A-THALASSEMIA ON PHENOTYPE IN IRAQI KURDS WITH HOMOZYGOUS AND COMPOUND HETEROZYGOUS SEVERE Β -THALASSEMIA.
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- Duhok Medical Journal, 2024, v. 18, n. 1, p. 77, doi. 10.31386/dmj.2024.18.1.9
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- Article
Non-transfusion-dependent thalassemia and thalassemia intermedia: epidemiology, complications, and management.
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- 2016
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- journal article
β -Thalassemia Intermedia Caused by Compound Heterozygosity for Hb Lepore-Hollandia and β -Thalassemia is Rare in the Indian Population.
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- 2015
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- Publication type:
- Case Study
Prevalence of Alpha and Beta-Thalassemia Mutations Among Carriers of Thalassemia in Shadegan City, Southwest of Iran.
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- Zahedan Journal of Research in Medical Sciences, 2015, v. 17, n. 8, p. 1, doi. 10.17795/zjrms1032
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- Article
Thalassaemiás betegen észlelt anaemia perniciosa - a diagnózis nehézségei.
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- Hungarian Medical Journal / Orvosi Hetilap, 2018, v. 159, n. 33, p. 1368, doi. 10.1556/650.2018.31097
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- Article
Co-inheritance of α-thalassaemia and β-thalassaemia in a prenatal screening population in mainland China.
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- Journal of Medical Screening, 2014, v. 21, n. 4, p. 167, doi. 10.1177/0969141314548203
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- Article
DETERMINANT FACTORS OF DEPRESSION IN BETA MAJOR THALASSEMIA CHILDREN.
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- Folia Medica Indonesiana (2355-8393), 2021, v. 57, n. 1, p. 46, doi. 10.20473/fmi.v57i1.24662
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- Article
ANALYSIS OF DEFERASIROX AND DEFERIPRON USE IN CHILDREN WITH PEDIATRIC β-THALASSEMIA MAJOR.
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- Folia Medica Indonesiana (2355-8393), 2016, v. 52, n. 1, p. 42
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- Article
Utilization of Discriminant Formulas in the Differentiation of Alpha Thalassemia, Beta Thalassemia, and Iron Deficiency in Premarital Setting.
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- Clinical Laboratory, 2021, v. 67, n. 4, p. 922, doi. 10.7754/Clin.Lab.2020.200644
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- Article
Mapping of the Beta-Thalassaemia Carrier in Sabah: An Initial Step to Strengthen the Thalassaemia Prevention Program in Malaysia.
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- Malaysian Journal of Medicine & Health Sciences, 2019, v. 15, p. 13
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- Article
Effectiveness of Multimodal Intervention Package to Assess the Nutritional Status & Psycho-Social Wellbeing among Children with Thalassemia Attending Thalassemia Unit of HSK Hospital & Research Center Bagalkot, Karnataka.
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- Indian Journal of Public Health Research & Development, 2020, v. 11, n. 8, p. 330
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- Article
Higher Serum Ferritin Levels Correlate with an Increased Risk of Cutaneous Morbidity in Adult Patients with β-Thalassemia: A Single-Center Retrospective Study.
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- Acta Haematologica, 2016, v. 135, n. 2, p. 124, doi. 10.1159/000438479
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- Article
Frequencies and phenotypic consequences of association of α- and β-thalassemia alleles with sickle-cell disease in Bahrain.
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- International Journal of Laboratory Hematology, 2017, v. 39, n. 1, p. 76, doi. 10.1111/ijlh.12577
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- Article
Molecular analysis of complex cases of alpha- and beta-thalassemia in Mexican mestizo patients with microcytosis and hypochromia reveals two novel alpha<sup>0</sup>-thalassemia deletions - -<sup>Mex1</sup> and - -<sup>Mex2</sup>.
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- International Journal of Laboratory Hematology, 2016, v. 38, n. 5, p. 535, doi. 10.1111/ijlh.12536
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- Article
Molecular understanding of Indian untransfused thalassemia intermedia.
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- International Journal of Laboratory Hematology, 2015, v. 37, n. 6, p. 791, doi. 10.1111/ijlh.12407
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- Article
Co-inherited β-thalassemia trait and HbH disease: clinical characteristics and interference in diagnosis of thalassemia by high-performance liquid chromatography.
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- International Journal of Laboratory Hematology, 2012, v. 34, n. 4, p. 427, doi. 10.1111/j.1751-553X.2012.01415.x
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- Article
Experience with combination of hydroxyurea and low-dose thalidomide in transfusion-dependent beta thalassemia patients.
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- 2021
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- Publication type:
- journal article
Evaluation of the Greek TranQol: a novel questionnaire for measuring quality of life in transfusion-dependent thalassemia patients.
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- 2017
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- Publication type:
- journal article
Genetic epidemiology of thalassemia in couples of childbearing age: over 6 years of a thalassemia intervention project.
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- Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-023-09091-z
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- Article
Magnetic Resonance Evaluation of Tissue Iron Deposition and Cardiac Function in Adult Regularly Transfused Thalassemia Intermedia Compared with Thalassemia Major Patients.
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- Journal of Clinical Medicine, 2024, v. 13, n. 16, p. 4791, doi. 10.3390/jcm13164791
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- Article
Gene Therapy: A Revolutionary Step in Treating Thalassemia.
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- Hematology Reports, 2024, v. 16, n. 4, p. 656, doi. 10.3390/hematolrep16040064
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- Article
Leg Ulcers: A Report in Patients with Hemoglobin E Beta Thalassemia and Review of the Literature in Severe Beta Thalassemia.
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- Acta Haematologica, 2022, v. 145, n. 3, p. 334, doi. 10.1159/000520731
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- Article
First Report on the Co-inheritance of Beta-globin IVS-l-5 (G→C) Thalassemia with Delta Globin CD12 {Asn→Lys (AAT→AAA)} HbA<sub>2</sub>- NYU in Iran.
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- Archives of Iranian Medicine (AIM), 2011, v. 14, n. 1, p. 8
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- Article
Elevated Hemoglobin A2 as a Marker for β-Thalassemia Trait in Pregnant Women.
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- Tohoku Journal of Experimental Medicine, 2011, v. 223, n. 3, p. 223, doi. 10.1620/tjem.223.223
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- Article
Detection of α-thalassaemia in neonates on cord blood and dried blood spot samples by capillary electrophoresis.
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- Malaysian Journal of Pathology, 2017, v. 39, n. 1, p. 17
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- Article
Thalassemia patients in transfussion dependent period and after hematopoietic stem cell transplantation: how are the psychiatric status and life quality of these patients?: (Assesment of patients with beta-thalassemia and in patients who underwent HSCT).
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- Pediatric Hematology & Oncology, 2023, v. 40, n. 7, p. 617, doi. 10.1080/08880018.2023.2220733
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- Article
Thalassemia Intermedia Caused by 16p13.3 Sectional Duplication in a β-Thalassemia Heterozygous Child.
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- Pediatric Hematology & Oncology, 2015, v. 32, n. 5, p. 349, doi. 10.3109/08880018.2015.1040932
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- Article
Quality of Life Assessment in Hematopoietic Stem Cell Transplantation Performed on Thalassemia Major Patients.
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- Pediatric Hematology & Oncology, 2012, v. 29, n. 5, p. 461, doi. 10.3109/08880018.2012.693577
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- Article
α-Thalassemia Frequency and Mutations in Children with Hypochromic Microcytic Anemias and Relation with β-Thalassemia, Iron Deficiency Anemia.
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- Pediatric Hematology & Oncology, 2012, v. 29, n. 3, p. 241, doi. 10.3109/08880018.2012.661831
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- Article
Detection of Early Cardiac Dysfunction in Patients with β-Thalassemia Major and Thalassemia Trait by Tissue Doppler Echocardiography.
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- Pediatric Hematology & Oncology, 2011, v. 28, n. 6, p. 486, doi. 10.3109/08880018.2011.568596
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- Article
PREVALENCE AND HEMATOLOGICAL CHARACTERISTICS OF β-THALASSEMIA TRAIT IN GAZIANTEP URBAN AREA, TURKEY.
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- Pediatric Hematology & Oncology, 2006, v. 23, n. 5, p. 419, doi. 10.1080/08880010600683400
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- Article
The Frequency and Importance of Common a-globin Gene Deletions Among p-Thalassemia Carriers in an Iranian Population.
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- Avicenna Journal of Medical Biotechnology, 2017, v. 9, n. 4, p. 196
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- Article
Cross-sectional Assessment of Physical Manifestations in Vietnamese Children with Thalassemia: A Single-Center Study.
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- Journal of Current Pediatrics / Guncel Pediatri, 2024, v. 22, n. 2, p. 74, doi. 10.4274/jcp.2024.33349
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- Article
Cell cycle, proliferation and apoptosis in erythroblasts cultured from patients with β-thalassaemia major.
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- British Journal of Haematology, 2016, v. 175, n. 3, p. 539, doi. 10.1111/bjh.13875
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- Article
Platelet and not erythrocyte microparticles are procoagulant in transfused thalassaemia major patients.
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- British Journal of Haematology, 2015, v. 171, n. 4, p. 615, doi. 10.1111/bjh.13609
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- Article
Prevalence of thalassemia in the Vietnamese population and building a clinical decision support system for prenatal screening for thalassemia.
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- Electronic Journal of General Medicine, 2023, v. 20, n. 4, p. 1, doi. 10.29333/ejgm/13206
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- Article
Dominant Beta Thalassemia: A Very Rare Cause of Thalassemia in a Mediterranean Country.
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- Hemoglobin, 2024, v. 48, n. 4, p. 258, doi. 10.1080/03630269.2024.2386067
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- Article
THALASSEMIA in ASIA 2021: Thalassemia in Guangxi Province, People's Republic of China.
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- Hemoglobin, 2022, v. 46, n. 1, p. 33, doi. 10.1080/03630269.2021.2008960
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- Article
Thalassemia in Asia 2021 Overview of Thalassemia and Hemoglobinopathies in Bangladesh.
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- Hemoglobin, 2022, v. 46, n. 1, p. 7, doi. 10.1080/03630269.2021.2008957
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- Article
Genetic Background of β-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new β<sup>0</sup>-Thalassemia Frameshift Mutation (HBB: c.374dup; p.Pro126Thrfs*15).
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- Hemoglobin, 2019, v. 43, n. 4/5, p. 223, doi. 10.1080/03630269.2019.1675689
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- Article
Krüppel-Like Factor 1 Gene Mutations in Thalassemia Patients from North Iran: Report of a New Mutation Associated with β-Thalassemia Intermedia.
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- Hemoglobin, 2019, v. 43, n. 1, p. 12, doi. 10.1080/03630269.2019.1567528
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- Article
Comparison of Quality of Life in Patients with β-Thalassemia Intermedia and β-Thalassemia Major in Southern Iran.
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- Hemoglobin, 2017, v. 41, n. 3, p. 169, doi. 10.1080/03630269.2017.1340307
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- Article
A Number of Cases in Iran Presenting with Coinheritance of Hemoglobin-H Disease and Beta-Thalassemia Minor.
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- Hemoglobin, 2016, v. 40, n. 5, p. 316, doi. 10.1080/03630269.2016.1220953
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- Article
Molecular Scanning of β -Thalassemia in the Southern Region of Central Java, Indonesia; a Step Towards a Local Prevention Program.
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- Hemoglobin, 2015, v. 39, n. 5, p. 330, doi. 10.3109/03630269.2015.1065420
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- Article