• A Case Report of Hemolytic Hyponatremia
• A de novo ANK1 mutation in a childhood hereditary spherocytosis: a case report
• A novel variant in the SPTB gene underlying hereditary spherocytosis and a literature review of previous variants
• A Rare Case of "Periportal Cuffing" as an Incidental Finding on ¹⁸F-FDG PET/CT
• A Rare Case of Iron Overload in Hereditary Spherocytosis: A Case Report
• A single-center cohort study of patients with hereditary spherocytosis in Central Europe reveals a high frequency of novel disease-causing genotypes
• A stepwise diagnostic approach for undiagnosed Anemia in children: A model for low-middle income country
• Accessory Spleen Mimicking an Intrahepatic Neoplasm: A Rare Case Report
• Aplastic crisis due to human parvovirus B19
• Applications of Flow Cytometry in Diagnosis and Evaluation of Red Blood Cell Disorders
• Atypical Course of Hereditary Spherocytic Anemia With Severely Elevated Liver Enzymes
• Case report: Genetic analysis of a novel intronic inversion variant in the <em>SPTB</em> gene associated with hereditary spherocytosis
• Case report: Genetic analysis of a novel intronic inversion variant in the SPTB gene associated with hereditary spherocytosis
• Catalase, Glutathione Peroxidase, and Peroxiredoxin 2 in Erythrocyte Cytosol and Membrane in Hereditary Spherocytosis, Sickle Cell Disease, and beta-Thalassemia
• Clinical and gene mutation characteristics of patients with hereditary ellipsocytosis: nine cases report and literature review
• Clinical and genetic characteristics of Chinese pediatric and adult patients with hereditary spherocytosis
• Clinical and genetic diagnosis for 26 paitents with hereditary spherocytosis
• Clinical and genotypic analysis of hereditary spherocytosis combined with cholestasis among pediatric patients
• Clinical Characteristics and Treatment Outcome of Hereditary Spherocytosis: A Single Center's Experience
• Clinical Exome Sequencing Reveals Novel Mutations in SPTB Gene Associated with Hereditary Spherocytosis in Patients with Suspected Congenital Hemolytic Anemia
• Clinical Presentation of Parvovirus B19 Infection in Adults Living with HIV/AIDS: A Case Series
• Coexistence of hereditary spherocytosis with SPTB P.Trp1150 gene variant and Gilbert syndrome: A case report and literature review
• Coinheritance of hereditary spherocytosis with haemochromatosis: next-generation sequencing reveals
• Comparative histological analysis of spleens in pediatric patients with hemolytic anemias: Insights into the pathophysiological mechanisms of spleen destruction in sickle cell anemia
• Complex heterozygous mutations in hereditary spherocytosis: A case report
• Concurrent Cholecystectomy Does Not Increase Splenectomy Morbidity in Patients With Hemolytic Anemia: A Pediatric NSQIP Analysis
• Consequence of Red Blood Cells Deformability on Heat Sink Effect of Blood in a Three-Dimensional Bifurcated Vessel
• Correction to: The Correlation Between Clinical Phenotype and Genotype of Hereditary Spherocytosis, by Hao Shen, et al. Genet Test Mol Biomarkers 2024; (vol. 28, no. 1; 33-38); doi: 10.1089/gtmb.2023.0307
• Could the 14q23.2 microdeletion or AKAP5 haploinsufficiency be a potential cause of intellectual disability?
• Designing a single-arm phase 2 clinical trial of mitapivat for adult patients with erythrocyte membranopathies (SATISFY): a framework for interventional trials in rare anaemias - pilot study protocol
• Enhanced Recovery after Surgery Applied to Pediatric Laparoscopic Cholecystectomy for Simple Cholelithiasis: Feasibility and Teaching Insights
• Exome-Based Trio Analysis for Diagnosis of the Cause of Congenital Severe Hemolytic Anemia in a Child
• Flow Cytometry as a New Accessible Method to Evaluate Diagnostic Osmotic Changes in Patients with Red Blood Cell Membrane Defects
• Genetic mutation analysis of hereditary spherocytosis in Guangxi Zhuang Autonomous Region
• Genotype-degree of hemolysis correlation in hereditary spherocytosis
• Giant lung tumor in hereditary spherocytosis: inflammatory myofibroblastic tumor
• Hematological characteristics and hepatobiliary complications of hereditary spherocytosis in a tertiary care pediatric center: optimizing diagnosis and care through local and international networks
• Hemochromatosis
• Hemolysis during open heart surgery in patients with hereditary spherocytosis - systematic review of the literature and case study
• Hemolytic anemia in a two-year-old child: A case of multiple red blood cell abnormalities
• Hereditary Spherocytosis
• Hereditary spherocytosis in a young female in Eastern Nepal: a case report
• Hereditary Spherocytosis with Mitochondrial Retention, Increased Oxidative Stress, and Alterations to Bioactive Membrane Lipids
• Hereditary Spherocytosis: Can Next-Generation Sequencing of the Five Most Frequently Affected Genes Replace Time-Consuming Functional Investigations?
• Hypercoagulability evaluation in congenital red blood cell disorders using thrombin generation assay
• Identification of a novel ANK1 gene variant c.1504-9G>A and its mechanism of intron retention in hereditary spherocytosis
• Influence of age and sex on osmoscan indies for next-generation osmotic gradient ektacytometry
• Integrative preimplantation genetic testing analysis for a Chinese family with hereditary spherocytosis caused by a novel splicing variant of <em>SPTB</em>
• Intragenic deletions in SPTB are associated with hereditary spherocytosis: Series of 12 cases
• Laparoscopic cholecystectomy for symptomatic cholelithiasis in children and adolescents: analysis of 50 cases from a single institution
• Laparoscopic concomitant cholecystectomy and splenectomy for true left-sided gall bladder with hereditary spherocytosis
• Long-term haematological response and maintained immunological function after laparoscopic subtotal splenectomy in patients with hereditary spherocytosis
• Membrane Protein Detection and Morphological Analysis of Red Blood Cells in Hereditary Spherocytosis by Confocal Laser Scanning Microscopy
• Minimal endoscopic sphincterotomy followed by papillary balloon dilation to relieve choledocholithiasis in a 6-year-old girl with hereditary spherocytosis
• Mitapivat reprograms red cell metabolome and improves anemia in a mouse model of hereditary spherocytosis
• Mitapivat reprograms the RBC metabolome and improves anemia in a mouse model of hereditary spherocytosis
• Molecular characteristics of hereditary red blood cell membrane disorders in Thailand: a multi-center registry
• Moyamoya syndrome secondary to hereditary spherocytosis: A case report
• Next generation sequencing (NGS) interest in deciphering erythrocyte molecular defects' association in red cell disorders: Clinical and erythrocyte phenotypes of patients with mutations inheritance in PIEZO1, Spectrin ß1, RhAG and SLC4A1
• Novel mutation in alpha-spectrin gene in Saudi patients with hereditary spherocytosis
• Piezo1 Regulation Involves Lipid Domains and the Cytoskeleton and Is Favored by the Stomatocyte-Discocyte-Echinocyte Transformation
• Porto-spleno-mesenteric venous thrombosis after elective splenectomy: a retrospective cohort study
• Precise diagnosis of a hereditary spherocytosis patient with complicated hematological phenotype
• Progression of hemolysis in a patient with hereditary spherocytosis after the second dose of COVID-19 mRNA vaccine: Correspondence
• Red blood cell senescence and vascular function in patients with hereditary spherocytosis with and without splenectomy
• Reticulocyte Antioxidant Enzymes mRNA Levels versus Reticulocyte Maturity Indices in Hereditary Spherocytosis, beta-Thalassemia and Sickle Cell Disease
• Retracted: Study on Management of Blood Transfusion Therapy in Patients with Hereditary Spherocytosis
• Robotic-Assisted Splenectomy by a Modified Lateral Approach: Technique and Outcomes
• Severe autoimmune hemolytic anemia complicating hereditary spherocytosis treated successfully with glucocorticoids and cyclosporine: a case report
• Severe hepatic sinusoidal obstruction syndrome in a patient with Wilms tumor and hereditary spherocytosis
• Simultaneous Robotic-Assisted Splenectomy and Cholecystectomy in Children: Is It Safe and Effective?
• Spherocytosis in Newborn Secondary to Novel Heterozygous Mutation in <em>SPTB</em> Gene: Case Report
• Splenic surgery in hematological diseases : Indications and surgical technique
• Temporal trends of splenectomy in pediatric hospitalizations with hereditary spherocytosis from 2000 to 2019: A national survey
• The coincidence of beta-thalassemia and hereditary spherocytosis: A case report and literature review
• The Correlation Between Clinical Phenotype and Genotype of Hereditary Spherocytosis
• Transcript-specific induction of stop codon readthrough using a CRISPR-dCas13 system
• Utility of Cryohemolysis Test in the Diagnosis of Hereditary Spherocytosis