Write in a clean editor, then format for Thalassemia Reports in one click — DocuGuru applies the official MDPI template with numbered references and exports a submission-ready PDF plus the editable LaTeX source. Free to start.
Thalassemia Reports is a peer-reviewed journal published by MDPI, covering Hemoglobinopathies and Related Disorders, Iron Metabolism and Disorders, Blood groups and transfusion. Over its lifetime it has published 302 papers, which have received 764 citations.
| Publisher | MDPI |
|---|---|
| Reference style | Numbered (MDPI) Numbered — [1], [2] in the text 1. Smith, A.; Jones, B.; Lee, C. A Representative Article Title. Thalassemia Reports 2023, 12, 45–58.
Formats any DOI in Thalassemia Reports style. No sign-up. |
| Abbreviation (ISO-4) | Thalass. Rep. |
| Publishes research in | Hemoglobinopathies and Related Disorders Iron Metabolism and Disorders Blood groups and transfusion Prenatal Screening and Diagnostics Erythrocyte Function and Pathophysiology |
| ISSN | 2039-4357 |
| Citation impact (2-yr) | 2.33 |
| h-index | 14 |
| i10-index | 22 |
| Article processing charge | $1,082 |
| Open access | Yes — indexed in DOAJ |
| Top institutions publishing here | Ospedale Vincenzo Cervello |
| Journal website | www.pagepressjournals.org |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Citations each year’s papers have accumulated so far — the most recent years are still building up.
Thalassemia represents a diverse group of inherited hematological disorders characterized by defective globin chain synthesis, leading to chronic anemia and associated complications. The complicated pathophysiology of beta-thalassemia involves genetic mutations or rarely deletions of the beta-globin gene on chromosome 11 whereas alpha-thalassemia involves deletions in the HBA1 and HBA2 genes or occasionally alterations to the…
Beta thalassemia is an inherited disorder resulting in abnormal or decreased production of hemoglobin, leading to hemolysis and chronic anemia. The long-term complications can affect multiple organ systems, namely the liver, heart, and endocrine. Myocardial iron overload is a common finding in β-thalassemia. As a result, different cardiovascular complications in the form of cardiomyopathy, pulmonary…
β-thalassemia, a congenital genetic hematological disorder characterized by the decrease or absence of β-globin chains, leads to a decrease in levels of Hemoglobin A. The affected individuals can be categorized into two cohorts based on transfusion dependency: transfusion-dependent thalassemia (TDT) and non-transfusion-dependent thalassemia (NTDT). Remarkably, despite the primary pathology lying in β-globin chain depletion, β-thalassemia…
The β-thalassemias and sickle cell disorders pose a major health burden in the large and diverse Indian population. Education programs for awareness generation are being done by National Institutions, non-governmental organizations and Thalassemia Societies in different states. Several extensive epidemiological studies have shown that there are many non-tribal and tribal communities where the prevalence of…
Abnormal iron accumulation in human tissues and oxidative damage are emerging issues in the medical field (1,2) [...]
