Changing Patterns of Thalassemia Worldwide

No abstract is available for this paper.

• Publication year

  2005

• Venue

  Annals of the New York Academy of Sciences

• Publication date

  2005-11-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.1196/annals.1345.003PMID 16339647
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with beta thalassemia.

  2004cited by this paper
• Cost‐effectiveness of prenatal screening for thalassaemia in Hong Kong

  2004cited by this paper
• Thalassemia in Sri Lanka: a progress report.

  2004cited by this paper
• Correction of hypercoagulability and amelioration of pulmonary arterial hypertension by chronic blood transfusion in an asplenic hemoglobin E/beta-thalassemia patient.

  2004cited by this paper
• Attenuation of oxidative stress-induced changes in thalassemic erythrocytes by vitamin E.

  2004cited by this paper
• Hemoglobin H disease: not necessarily a benign disorder.

  2003cited by this paper
• The molecular basis for the thalassaemias in Sri Lanka

  2003cited by this paper
• The effects of vitamin E on platelet activity in beta-thalassaemia patients.

  2003cited by this paper
• In vivo Platelet Activation and Hyperaggregation in Hemoglobin E/β-Thalassemia: A Consequence of Splenectomy

  2003cited by this paper
• Extramedullary haemopoiesis in haemoglobin E/beta-thalassaemia.

  2003cited by this paper
• The effects of vitamin E on platelet activity in β‐thalassaemia patients

  2003cited by this paper
• The hypercoagulable state in thalassemia.

  2002cited by this paper
• Relationship between hypercoagulable state and erythrocyte phosphatidylserine exposure in splenectomized haemoglobin E/β‐thalassaemic patients *

  2002cited by this paper
• Hb H hydrops foetalis syndrome: a case report and review of literature

  2001cited by this paper
• Universal Newborn Screening for Hb H Disease in California

  2001cited by this paper
• Inherited haemoglobin disorders: an increasing global health problem.

  2001cited by this paper
• 1999 international conference on E-β thalassemia.

  2000cited by this paper
• Outreach Strategies for Southeast Asian Communities: Experience, Practice, and Suggestions for Approaching Southeast Asian Immigrant and Refugee Communities to Provide Thalassemia Education and Trait Testing

  2000cited by this paper
• Hemoglobin F and hemoglobin E/beta-thalassemia.

  2000cited by this paper
• Genetic and clinical features of hemoglobin H disease in Chinese patients.

  2000cited by this paper
• Thalassaemia in Sri Lanka: implications for the future health burden of Asian populations. Sri Lanka Thalassaemia Study Group.

  2000cited by this paper
• Clinical Manifestation of &bgr;-Thalassemia/Hemoglobin E Disease

  2000cited by this paper
• Clinical and hematologic aspects of hemoglobin E beta-thalassemia.

  2000cited by this paper
• Clinical and hematologic aspects of hemoglobin E β-thalassemia

  2000cited by this paper
• Changing outcome of homozygous alpha-thalassemia: cautious optimism.

  2000cited by this paper
• Asian Immigration and Public Health in California: Thalassemia in Newborns in California

  2000cited by this paper
• Global Epidemiology of Hemoglobin Disorders

  1998cited by this paper
• Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem

  1998cited by this paper
• Hydrops fetalis caused by alpha-thalassemia: an emerging health care problem.

  1998cited by this paper
• The unusual pathobiology of hemoglobin constant spring red blood cells.

  1997cited by this paper
• Prevalence and genotypes of alpha‐ and beta‐thalassemia carriers in Hong Kong — Implications for population screening

  1997cited by this paper
• Prevalence and genotypes of α- and β-thalassemia carriers in Hong Kong : Implications for population screening

  1997cited by this paper

• Overcoming transfusion-refractory anemia: partial splenic embolization to facilitate orthopedic surgery in β-thalassemia

  2026cites this paper
• Transforming the treatment of Alpha-Thalassemia: a single-center retrospective study on hematopoietic stem cell transplantation in transfusion-dependent pediatric patients

  2026cites this paper
• The Heterogeneous Global Burden of Hemoglobinopathies Among Women of Childbearing Age, 1990-2021, with Projection to 2030

  2026cites this paper
• Molecular Docking and Dynamics of Natural Compounds Targeting Iron and Erythropoietic Pathways in β-Thalassemia

  2026cites this paper
• Deep Neural Networks for Optimal Donor Matching in HLA-Haploidentical Transplantation

  2025influential citation
• Retinal Complications in a Patient With Pediatric Thalassemia: A Case Report

  2025cites this paper
• Assessment of β-Thalassemia Trait Occurrence in an Outpatient Sample from Southern Chile: A Retrospective Study

  2025cites this paper
• EVALUATION OF VITAMIN D, CALCIUM, LFTS IN BETA THALASSEMIA PATIENTS

  2025influential citation
• Multifocal Keratitis in 23-year-old Woman with β-Thalassemia

  2025cites this paper
• Evaluated NSUN3 in reticulocytes from HbH-CS disease that reflects cellular stress in erythroblasts

  2025cites this paper
• From CBC to clarity: Interpretable detection of beta-thalassemia carriers in imbalanced datasets

  2025cites this paper
• Determinants of Multi-Organ Morbidity in Neo-Transfusion-Dependent Thalassemia: A Cross-Sectional Analysis

  2025cites this paper
• Efficacy and safety of hydroxyurea therapy on patients with β-thalassemia: a systematic review and meta-analysis

  2025cites this paper
• Analysis of genotypic distribution and rare variants of patients with α/β-thalassemia screened in one hospital in Beijing, China

  2025cites this paper
• Skin Peeling of Palm-Sole and Chronic Depression Associated with E-trait or E-disease- Case Series

  2025cites this paper
• Hemoglobinopathies & Types: Overview, Pathophysiology, and Epidemiology

  2025cites this paper
• Alpha+ Thalassemia in Northwestern Tanzania: Molecular and Hematological Insights From Newborn Screening

  2025cites this paper
• Liver steatosis in patients with transfusion‐dependent thalassaemia

  2024cites this paper
• Αlpha-thalassemia: A practical overview.

  2024cites this paper
• Case report: A rare heterozygous Hb CS with heterozygous HbE in a family with thalassemia in China

  2024cites this paper
• Ocular Involvement in Children with Beta-Thalassemia Major

  2024cites this paper
• Hemoglobinopathies in the Neonate.

  2024cites this paper
• Development of molecular diagnostic platform for α0‐thalassemia 44.6 kb (Chiang Rai, ‐‐CR) deletion in individuals with microcytic red blood cells across Thailand

  2023cites this paper
• Comparison of screening indicators for different types of thalassemia carriers in Hunan Province

  2023cites this paper
• Labile plasma iron and echocardiographic parameters are associated with cardiac events in β‐thalassemic patients

  2023cites this paper
• Does thalassemia truly cause microvascular changes without us noticing? An optical coherence tomography angiography study of the children with beta-thalassemia

  2023cites this paper
• Reducing erythroblast apoptosis in β-thalassemia via unfolded protein response (UPR) signaling

  2023cites this paper
• Transfusion Complications in Thalassemia: Patient Knowledge and Perspectives

  2022cites this paper
• COMPARATIVE EFFICACY AND SAFETY OF ORAL IRON CHELATORS AND THEIR NOVEL COMBINATION IN CHILDREN WITH THALASSEMIA

  2022cites this paper
• Impact of Hydroxyurea on Blood Transfusion Rate in Patients of Beta-Thalassemia Major

  2022cites this paper
• Molecular characterization of HBB gene mutations in beta-thalassemia patients of Southern Iraq

  2022cites this paper
• Alpha-Thalassemia: Diversity of Clinical Phenotypes and Update on the Treatment

  2022influential citation
• A Review of Iron Overload in Beta-Thalassemia Major, and a Discussion on Alternative Potent Iron Chelation Targets

  2022cites this paper
• Genetic Analysis of Alpha-Thalassemia Mutations in Thi-Gar Province, Iraq.

  2022cites this paper
• Nutritional Status in a Sample of Patients With β-Thalassemia Major

  2022cites this paper
• Psychological distress and coping strategies among the caretakers of children with transfusion-dependent thalassemia

  2022cites this paper
• Hybrid Model for Prediction of Treatment Response in Beta-thalassemia Patients with Hepatitis C Infection

  2021cites this paper
• Association between left ventricular strain and cardiac iron load in beta-thalassaemia major: a cardiac magnetic resonance study

  2021cites this paper
• Current status of beta‐thalassemia and its treatment strategies

  2021cites this paper
• Assessment of level of Awareness regarding Thalassemia Major among Parents of Affected Children

  2021cites this paper
• Macular microvascular changes in children with transfusion-dependent beta-thalassemia

  2021cites this paper
• Classification of β-Thalassemia Carriers From Red Blood Cell Indices Using Ensemble Classifier

  2021cites this paper
• Thyroid pro le in patients of thalassemia with multiple blood transfusions and high serum ferritin: a cross-sectional study

  2021cites this paper
• Immigration and screening programs for hemoglobinopathies in Italy, Spain and Turkey

  2021cites this paper
• Serum ferritin levels and it’s correlation with cardiac iron overload with the help of cardiac T2* magnetic resonance imaging

  2021cites this paper
• Identification of optimal thalassemia screening strategies for migrant populations in Thailand using a qualitative approach

  2021cites this paper
• Allele Amplification Failure in the HBB Gene due to Allelic Dropoutin a Pre-Preimplantation Genetic Testing (pre-PGT) Case

  2021cites this paper
• A Review on Epidemiology and Thalassemia Distribution, in Relevance to United Arab Emirates Population

  2021influential citation
• Ayurvedic add-on therapy for β-Thalassemia major cases on quality of life: A case series

  2021cites this paper
• The worldwide molecular spectrum and distribution of thalassaemia: a systematic review

  2021cites this paper
• Mapping PedsQL™ Generic Core Scales to EQ-5D-3L utility scores in transfusion-dependent thalassemia patients

  2021cites this paper
• Assessment of molecular and clinical characteristics in blood transfusion dependent HbE/β-thalassemia patients

  2021cites this paper
• Retinal and Choriocapillaris Vascular Changes in Patients Affected by Different Clinical Phenotypes of β-Thalassemia: An Optical Coherence Tomography Angiography Study

  2021cites this paper
• Feasibility of and barriers to thalassemia screening in migrant populations: a cross-sectional study of Myanmar and Cambodian migrants in Thailand

  2021cites this paper
• Uncover molecular network between beta thalassemia and retinal abnormality through in silico study

  2021cites this paper
• Bayesian spatial modeling of transfusion-dependent β-thalassemia incidence rate in Fars Province, Southern Iran.

  2021cites this paper
• Beta Thalassemia Minor: Patients Are Not Tired but Depressed and Anxious

  2020cites this paper
• An Evaluation of Bone Health Parameters in Regularly Transfused Beta-Thalassemia Major Patients

  2020cites this paper
• Adherence and Satisfaction of Deferasiroxversus Deferoxamine in Transfusion-Dependent Beta-Thalassemia

  2020cites this paper
• Serum Salusin-α and Salusin -b levels with some Biochemical Parameters in Patients with Major Thalassemia

  2020cites this paper
• The effect of mother’s β-thalassemia minor on placental histology and neonatal outcomes

  2020cites this paper
• Nature and severity of dental malocclusion in children suffering from transfusion-dependent (-thalassemia major

  2020cites this paper
• Demographic and History Related Treatment Status of Thalassaemia Patients in a Tertiary Hospital in Bangladesh

  2020cites this paper
• Epidemiology of Thalassemia in Gulf Cooperation Council Countries: A Systematic Review

  2020influential citation
• Protective Effects of Selenium in Patients with Beta-Thalassemia Major

  2020cites this paper
• Utility of screening tools to differentiate beta thalassemia trait and iron-deficiency anemia - do they serve a purpose in blood donors?

  2020cites this paper
• Prevalence of Congenital Hemolytic Disorders in Denmark, 2000–2016

  2020cites this paper
• Review on Thalassemia Epidemiology and Managementin Children

  2020cites this paper
• PREVALENCE OF HEMOGLOBINOPATHIES IN THE POPULATION OF DIBRUGARH AND IT'S ASSOCIATION WITH SEX

  2020cites this paper
• Quantitative determination of HbA2 level in β-thalassemia trait by using Capillary Electrophoresis in Balochistan

  2020cites this paper
• Hemoglobinopathies in Iran: An Updated Review

  2020cites this paper
• Random Forest Analysis: A New Approach for Classification of Beta Thalassemia

  2020cites this paper
• Prevalence and molecular characterization of alpha-thalassemia among newborns in Ardabil Province

  2020cites this paper
• Quantitative determination of HbA2 level in β-thalassemia trait by using Capillary Zone Electrophoresis in Balochistan; A comparative study

  2020cites this paper
• Prevalence of Malocclusion in Patients with Thalassemia Major: A Cross-sectional Study

  2020cites this paper
• Frequency and Risk Factors of Red Blood Cell Alloimmunization in Thalassemia Major Patients in Markazi province

  2019cites this paper
• Childbearing through the Lens of Women with Minor Thalassemia: A Qualitative Study

  2019cites this paper
• A Pilot Optical Coherence Tomography Angiography Study on Superficial and Deep Capillary Plexus Foveal Avascular Zone in Patients With Beta-Thalassemia Major.

  2019cites this paper
• Serum Ferritin Correlated With Deficiency of Serum Vitaminb12 and Folic Acid in Thalassemia

  2019cites this paper
• Retina A Pilot Optical Coherence Tomography Angiography Study on Superficial and Deep Capillary Plexus Foveal Avascular Zone in Patients With Beta-Thalassemia Major

  2019cites this paper
• The frequency of iron deficiency anemia and beta thalassemia carriers involunteers of marriage

  2019cites this paper
• The Genetic Determinants for Long-term Response to Hydroxyurea Therapy in Indian β-Thalassemia Patients

  2019cites this paper
• Alpha‐globin gene mutation spectrum in patients with microcytic hypochromic anemia from Mazandaran Province, Iran

  2019cites this paper
• Cardiac T2* magnetic resonance analysis of membranous interventricular septum in assessment of cardiac iron overload in pediatric thalassemia patients: A pilot study

  2019cites this paper
• Splenectomy for people with thalassaemia major or intermedia.

  2019cites this paper
• MOLECULAR IDENTIFICATION OF CLINICAL MICROBES IN THALASSEMIA PATIENTS USING 16S rRNA GENE SEQUENCING

  2019cites this paper
• Diagnosis of thalassemia using fluorescence spectroscopy, auto-analyzer, and hemoglobin electrophoresis - A prospective study.

  2019cites this paper
• Providers’ Perspectives on Treating Patients With Thalassemia

  2019cites this paper
• Presidential address

  2019cites this paper
• New methods for thalassemia screening: TGA/Chemometrics test is not influenced by the aging of blood samples

  2019cites this paper
• Detection of some antioxidant markers in saliva of patients with beta thalassemia major

  2019cites this paper
• Disruption of the MBD2-NuRD complex but not MBD3-NuRD induces high level HbF expression in human adult erythroid cells

  2019cites this paper
• The Spectrum of β-Thalassemia Mutations in Siirt Province, Southeastern Turkey

  2019cites this paper
• The ASPHO 2019 distinguished career award goes to Dr. Elliott P. Vichinsky

  2019cites this paper
• Non-invasive Prenatal Diagnosis of β-Thalassemia by Detection of the Cell-Free Fetal DNA in Maternal Circulation

  2019cites this paper
• Economic Evaluation of Chelation Regimens for β-Thalassemia Major: a Systematic Review

  2019cites this paper
• Increased endothelial activation in α-thalassemia disease

  2019cites this paper
• The effect of educational program based on theory of planned behavior on health promotion and childbearing of minor thalassemia couples

  2019cites this paper
• EXPECTATIONS FOR LIFE AMONG GREEK TEENAGE THALASSAEMICS

  2018cites this paper
• Update on thalassemia diagnosis: New insights and methods.

  2018cites this paper