Yearly Publication Trends - thalassemia patients

Year	Publication Count
2024	376
2023	1144
2022	611
2021	496
2020	451
2019	394
2018	246
2017	256
2016	223
2015	154
2014	173

Relevant Publications

Red Cell Alloimmunisation Among Sickle Cell Disease and Thalassemia Patients Following Rh- and K-Matched Red Cell Transfusion in Southwestern Saudi Arabia: A Multicenter Study.

Issue Release: 2024

Optimizing the management of inherited blood disorders in a changing market: Findings from the AMCP Market Insights Program.

Issue Release: 2024

Awareness and practical evaluation of correct use of iron chelators; a study to track the ambiguities of thalassemia patients on their medications in Iran.

Issue Release: 2024

Prenatal Diagnosis of Cystic Fibrosis by Celocentesis.

Issue Release: 2024

Catalase, Glutathione Peroxidase, and Peroxiredoxin 2 in Erythrocyte Cytosol and Membrane in Hereditary Spherocytosis, Sickle Cell Disease, and β-Thalassemia.

Issue Release: 2024

How I treat iron overload in adult myelodysplastic syndrome.

Issue Release: 2024

Early Detection of Renal Complication in Children With Sickle Cell Disease: A Single Center Prospective Study.

Issue Release: 2024

Factors Associated With Quality of Life Among Adolescent With Beta Thalassemia in Indonesia: A Cross-Sectional Study.

Issue Release: 2024

Routine antenatal molecular testing for α-thalassemia at a tertiary referral hospital in China: ten years of experience.

Issue Release: 2024

Endoscopic manifestation of intestinal transplant-associated microangiopathy after stem cell transplantation.

Issue Release: 2024

Multiparametric cardiac magnetic resonance in patients with thalassemia intermedia: new insights from the E-MIOT network.

Issue Release: 2024

Differential effects of iron chelators on iron burden and long-term morbidity and mortality outcomes in a large cohort of transfusion-dependent β-thalassemia patients who remained on the same monotherapy over 10 years.

Issue Release: 2024

Survival of transfused red blood cells from a donor with alpha-thalassemia trait in a recipient with sickle cell disease.

Issue Release: 2024

COVID-19 presenting as severe acute hepatitis in a pediatric patient with thalassemia minor: A case report.

Issue Release: 2024

Modified lentiviral globin gene therapy for pediatric β/β transfusion-dependent β-thalassemia: A single-center, single-arm pilot trial.

Issue Release: 2024

Clinical Practice Patterns in Sickle Cell Disease Treatment: Disease-Modifying and Potentially Curative Therapies.

Issue Release: 2024

Elevating fetal hemoglobin - recently discovered regulators and mechanisms.

Issue Release: 2024

Iron chelation therapy for children with transfusion-dependent β-thalassemia: How young is too young?

Issue Release: 2024

New Born Screening of Hemoglobinopathies in a Center Tunisian Population.

Issue Release: 2024

Nutritional and Body Composition Changes in Paediatric β-Thalassemia Patients Undergoing Hematopoietic Stem Cell Transplantation: A Retrospective Study Using Bioelectrical Impedance Analysis.

Issue Release: 2024

What Are Developmental Disorders?

How Do Genetic Mutations Cause Cystic Fibrosis?

What is Polyploidy?

Which Gene is Involved?

What Types of Genetic Mutations Can Be Treated?

What Are the Challenges in Phylogenetic Analysis?

What Are Some Examples of Gene Amplification in Disease?

What is Genetic Engineering?

Can Infectious Diseases Cause Genetic Mutations?

Can Autosomal Recessive Disorders be Treated or Managed?

Yearly Publication Trends - thalassemia patients

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