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Last Updated: 10/31/2025

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Found 1163 publications

Clinical and hematological characteristics of beta-plus thalassemia and uncommon beta-chain hemoglobin variants in Northern Thailand.

Clinical and hematological characteristics of beta-plus thalassemia and uncommon beta-chain hemoglobin variants in Northern Thailand.

Journal: Annals of medicine
Published: September 01, 2025

A Diagnostic Pitfall: Hidden Hazards of Lead Neuropathy by Co-Existence of Hemoglobinopathy and Cervical Radiculomyelopathy.

A Diagnostic Pitfall: Hidden Hazards of Lead Neuropathy by Co-Existence of Hemoglobinopathy and Cervical Radiculomyelopathy.

Journal: Clinical case reports
Published: April 29, 2025

Genetic polymorphism of novel SNP rs5006884 in OR51B6 and SNP rs4499252 in AHSP among transfusion-dependent and non-transfusion-dependent β-thalassemia/Hb E patients in Thailand: a multivariate analysis of clinical and genetic polymorphism.

Genetic polymorphism of novel SNP rs5006884 in OR51B6 and SNP rs4499252 in AHSP among transfusion-dependent and non-transfusion-dependent β-thalassemia/Hb E patients in Thailand: a multivariate analysis of clinical and genetic polymorphism.

Journal: Annals of hematology
Published: February 17, 2025

Usefulness of the AHEAD score for prediction of all-cause death in patients with acute and chronic coronary syndromes.

Usefulness of the AHEAD score for prediction of all-cause death in patients with acute and chronic coronary syndromes.

Journal: International journal of cardiology. Cardiovascular risk and prevention
Published: February 17, 2025

Biochemical and Molecular Effects of Gadolinium and Lanthanum on Chironomus sancticaroli (Diptera: Chironomidae).

Biochemical and Molecular Effects of Gadolinium and Lanthanum on Chironomus sancticaroli (Diptera: Chironomidae).

Journal: Archives of environmental contamination and toxicology
Published: February 07, 2025

Prevalence of double heterozygotes of HbE and α-thal 1 (SEA) type in pregnancies and their partners that received antenatal care at Chiangrai Prachanukroh Hospital and reevaluated the cut-offs for differentiation.

Prevalence of double heterozygotes of HbE and α-thal 1 (SEA) type in pregnancies and their partners that received antenatal care at Chiangrai Prachanukroh Hospital and reevaluated the cut-offs for differentiation.

Journal: PloS one
Published: February 06, 2025

Survival and thalassaemia-related complications in HbE/beta-thalassaemia and alpha-thalassaemia: A 10-year longitudinal study in Thailand.

Survival and thalassaemia-related complications in HbE/beta-thalassaemia and alpha-thalassaemia: A 10-year longitudinal study in Thailand.

Journal: British journal of haematology
Published: February 06, 2025

Rapid Identification of β-Thalassemia, Hb E, and High Hb F Determinants Using a High-Resolution Melting Analysis: Application in Prenatal Diagnosis in Southern Thailand.

Rapid Identification of β-Thalassemia, Hb E, and High Hb F Determinants Using a High-Resolution Melting Analysis: Application in Prenatal Diagnosis in Southern Thailand.

Journal: Hemoglobin
Published: February 04, 2025

Disrupting ZBTB7A or BCL11A binding sites reactivates fetal hemoglobin in erythroblasts from healthy and β0-thalassemia/HbE individuals.

Disrupting ZBTB7A or BCL11A binding sites reactivates fetal hemoglobin in erythroblasts from healthy and β0-thalassemia/HbE individuals.

Journal: Scientific reports
Published: January 21, 2025

Novel HBB:c.375_376delAC mutation in a Malay patient with HbE beta-thalassemia intermedia: A case report.

Novel HBB:c.375_376delAC mutation in a Malay patient with HbE beta-thalassemia intermedia: A case report.

Journal: Medicine
Published: January 16, 2025

Generation of an integration-free induced pluripotent stem cell line, MURAi006-A, from a hemoglobin E/β-thalassemia patient harboring the βE/β0 (Codon 17, A > T) compound heterozygous mutation.

Generation of an integration-free induced pluripotent stem cell line, MURAi006-A, from a hemoglobin E/β-thalassemia patient harboring the βE/β0 (Codon 17, A > T) compound heterozygous mutation.

Journal: Stem cell research
Published: January 08, 2025

Unveiling Rare Hemoglobinopathies: Hematologic Characterization of Double Heterozygous Hb D and Hb E With Beta-Thalassemia-A Case Report.

Unveiling Rare Hemoglobinopathies: Hematologic Characterization of Double Heterozygous Hb D and Hb E With Beta-Thalassemia-A Case Report.

Journal: Case reports in hematology
Published: December 17, 2024
Showing 1-12 of 1,163

Last Updated: 10/31/2025