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Last Updated: 01/07/2026

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Found 1169 publications

Castleman Disease in a Child: A Rare Cause of Persistent Cervical Lymphadenopathy.

Castleman Disease in a Child: A Rare Cause of Persistent Cervical Lymphadenopathy.

Journal: Cureus
Published: November 07, 2025

A Rare Severe Hemolytic Crisis in Homozygous Hemoglobin E (HbEE).

A Rare Severe Hemolytic Crisis in Homozygous Hemoglobin E (HbEE).

Journal: Hemoglobin
Published: October 28, 2025

Application of Artificial Intelligence in Sickle Cell Identification From Blood Smears: A Potential Game Changer for Developing Nations.

Application of Artificial Intelligence in Sickle Cell Identification From Blood Smears: A Potential Game Changer for Developing Nations.

Journal: Cureus
Published: October 27, 2025

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

Serum erythropoietin and its determinants and associations in patients with haemoglobin E β-thalassaemia.

Serum erythropoietin and its determinants and associations in patients with haemoglobin E β-thalassaemia.

Journal: Scientific reports
Published: July 15, 2025

Accurate diagnosis of hemoglobinopathies with machine learning based on high-throughput proteomics.

Accurate diagnosis of hemoglobinopathies with machine learning based on high-throughput proteomics.

Journal: HemaSphere
Published: May 03, 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

Molecular and structural characterization of a novel β-hemoglobinopathy caused by in Cis β-globin mutations in a Thai individual.

Molecular and structural characterization of a novel β-hemoglobinopathy caused by in Cis β-globin mutations in a Thai individual.

Journal: Scientific reports
Published: March 11, 2025

Multi-centric origins and gene flow shape the diversity of β-thalassemia mutations in Southern East Asia.

Multi-centric origins and gene flow shape the diversity of β-thalassemia mutations in Southern East Asia.

Journal: Nature communications
Published: February 18, 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

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
Showing 1-12 of 1,169

Last Updated: 01/07/2026