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2 Am J Hematol |
Retrieve available abstracts of this week’s articles:
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AMEDEO Anemia is free of charge.
Efficacy of Single-Dose Intravenous Ferric Derisomaltose for Iron Deficiency
Anemia in Pregnancy.
Am J Hematol. 2026 Jan 2. doi: 10.1002/ajh.70190.
PubMed
Abstract available
Acute Exercise Challenge and Airway Dynamics in Youth With Sickle Cell Anemia: A
Multicenter Study.
Am J Hematol. 2025 Dec 20. doi: 10.1002/ajh.70170.
PubMed
Abstract available
NMNAT3 deficiency: a novel red blood cell enzymopathy causing hemolysis by
altering NAD levels and glycolysis.
Blood. 2025;146:3246-3249.
PubMed
Abstract available
The double burden: co-occurrence of malaria and anaemia in children under five in
Ghana - a multilevel mixed-effects logistic regression analysis.
BMC Pediatr. 2025;25:1000.
PubMed
Abstract available
Nonsense Variant in the beta-Spectrin Gene Causing Hereditary Spherocytosis
Identified by Whole-Exome Sequencing in a Child.
Hemoglobin. 2025;49:439-443.
PubMed
Abstract available
Identification of a Patient with Transfusion-Dependent beta-Thalassemia Caused by
Compound Heterozygous Mutations of HBB: C.84_85insC and Common Linked Intronic
Variants in HBB.
Hemoglobin. 2025;49:429-434.
PubMed
Abstract available
A Cross-Sectional Study on Pain and Quality of Life of Adult Patients with
Transfusion-Dependent Thalassemia in a Tertiary Hospital In Malaysia.
Hemoglobin. 2025;49:399-407.
PubMed
Abstract available
Predicting the Double Heterozygotes of HbE and alpha-Thalassemia-1 (Southeast Asian
Type) Using RapidMiner-Generated Hematologic Algorithm.
Hemoglobin. 2025;49:390-398.
PubMed
Abstract available
Genetic Analysis and Clinical Relevance of HBA1:c.305T > C (Leu > Pro): A Novel
Variant Linked to alpha-Thalassemia.
Hemoglobin. 2025;49:424-428.
PubMed
Abstract available
Genetically Confirmed Dual Hematologic Disorder: A Case of beta-Thalassemia with
Frameshift Mutation and Type 3 von Willebrand Disease in a Pediatric Patient.
Hemoglobin. 2025;49:421-423.
PubMed
Abstract available
A Diverse Genetic Landscape: Thalassemia Genotype Patterns in Myanmar and
Cambodian Workers in Southern Thailand.
Hemoglobin. 2025;49:384-389.
PubMed
Abstract available
Pituitary Versus Hepatic Iron Assessment in Transfusion-Dependent Thalassemia: Is
Signal Intensity Ratio a Reliable Tool?
Hemoglobin. 2025;49:377-383.
PubMed
Abstract available
Genotypic Characterization of Thalassemia in Huadu District, Guangzhou, China: A
Single-Center Retrospective Study.
Hemoglobin. 2025;49:371-376.
PubMed
Abstract available
Utility of Molecular Sequencing and Hematologic Parameters for Diagnosis of
alpha-Thalassemia: A Perspective of the National Reference Laboratory.
Hemoglobin. 2025;49:414-420.
PubMed
Abstract available
Lnk Deficiency Enhances Translesion Synthesis to Alleviate Replication Stress and
Promote Hematopoietic Stem Cell Fitness.
J Clin Invest. 2025 Oct 30:e191713. doi: 10.1172/JCI191713.
PubMed
Abstract available
Increased Red Blood Cell Count With High Hemoglobin Indicates a Different
Diagnosis From Beta-thalassemia Trait, Regardless of Mean Corpuscular Volume:
Hereditary Hemochromatosis-A Retrospective Analysis.
J Pediatr Hematol Oncol. 2026;48:e51-e54.
PubMed
Abstract available
Shock and Severe Anemia in a Pediatric Patient.
Pediatr Rev. 2026;47:64-66.
PubMed
Outcomes of Universal Newborn G6PD Deficiency Screening in a Large Urban Cohort.
Pediatrics. 2025 Dec 2:e2025072850. doi: 10.1542/peds.2025-072850.
PubMed
Abstract available
Is glucose-6-phosphate dehydrogenase deficiency associated with COVID-19
infection, severity, and death? A cohort study from the Brazilian Amazon.
PLoS One. 2025;20:e0331729.
PubMed
Abstract available
Thank you for your interest in scientific medicine.