Disease: Anemia- hereditary spherocytic hemolytic
- <em>PIEZO1</em> Hypomorphic Variants in Congenital Lymphatic Dysplasia Cause Shape and Hydration Alterations of Red Blood Cells
- A case of acute opisthorchiasis concurrent with chronic hereditary hemolytic anemia
- A comparative evaluation of Eosin-5'-maleimide flow cytometry reveals a high diagnostic efficacy for hereditary spherocytosis
- A de novo ANK1 mutation associated to hereditary spherocytosis: a case report
- A neonate with Coombs-negative hemolytic jaundice with spherocytes but normal erythrocyte indices: a rare case of autosomal-recessive hereditary spherocytosis due to alpha-spectrin deficiency
- A new simple approach for the determination of pyrimidine 5'-nucleotidase activity in human erythrocytes using an ELISA reader
- A Novel <em>de novo</em> Mutation in <em>ANK1</em> Gene Identified through Targeted Next-Generation Sequencing in a Neonate with Hereditary Spherocytosis
- A novel <em>SPTB</em> gene mutation in neonatal hereditary spherocytosis: A case report
- A novel binding of GTP stabilizes the structure and modulates the activities of human phosphoglucose isomerase/autocrine motility factor
- A Novel de novo Mutation in ANK1 Gene Identified through Targeted Next-Generation Sequencing in a Neonate with Hereditary Spherocytosis
- A novel SPTB gene mutation in neonatal hereditary spherocytosis: A case report
- A novel SPTB mutation causes hereditary spherocytosis via loss-of-function of beta-spectrin
- A novel SPTB mutation causes hereditary spherocytosis via loss-of-function of β-spectrin
- Advances in laboratory diagnosis of hereditary spherocytosis
- An ANK1 IVS3-2A>C mutation causes exon 4 skipping in two patients from a Chinese family with hereditary spherocytosis
- Anaemia caused by a congenital haemoglobin defect can also occur in native Dutch patients
- Aplastic crisis due to parvovirus B19 and Epstein-Barr virus in a patient with hereditary spherocytosis
- Atypical Course of Hereditary Spherocytic Anemia With Severely Elevated Liver Enzymes
- Biallelic hexokinase 1 (HK1) variants causative of non-spherocytic haemolytic anaemia: A case series with emphasis on the HK1 promoter variant and literature review
- Case report: A follow up of a major pelvic splenosis
- Case report: A rare case of pyruvate kinase deficiency and Crigler-Najjar syndrome type II with a novel pathogenic variant of <em>PKLR</em> and <em>UGT1A1</em> mutation
- Chronic haemolytic icterus resembling acholuric jaundice occurring in an African native
- Compound Heterozygosity for <em>KLF1</em> Mutations Causing Hemolytic Anemia in Children: A Case Report and Literature Review
- Compound Heterozygosity for KLF1 Mutations Causing Hemolytic Anemia in Children: A Case Report and Literature Review
- Congenital Dyserythropoietic Anemia Type II With Myelofibrosis in an Adult Patient: A Report of a Rare Case With a Brief Review
- Congenital hemolytic jaundice in a Negro family
- Consensus document for the diagnosis and treatment of pyruvate kinase deficiency
- De novo variants in HK1 associated with neurodevelopmental abnormalities and visual impairment
- Detection of red blood cell antibodies in mitogen-stimulated cultures from patients with hereditary spherocytosis
- Diagnosing dehydrated hereditary stomatocytosis due to a <em>KCNN4</em> Gardos channel mutation: understanding challenges through study of a multi-generational family
- Diagnosing dehydrated hereditary stomatocytosis due to a KCNN4 Gardos channel mutation: understanding challenges through study of a multi-generational family
- Early postnatal diagnosis of hereditary spherocytosis by combining light microscopy, acidified glycerol lysis test and eosin-5'-maleimide binding assay
- Effect of elective surgery on subjective health in veterans with chronic posttraumatic stress disorder
- Effects of <em>SPTA1</em> Gene Variants on the Hematological Phenotype of Mexican Patients with Hereditary Spherocytosis
- Effects of SPTA1 Gene Variants on the Hematological Phenotype of Mexican Patients with Hereditary Spherocytosis
- Ektacytometry Analysis of Post-splenectomy Red Blood Cell Properties Identifies Cell Membrane Stability Test as a Novel Biomarker of Membrane Health in Hereditary Spherocytosis
- Elevated levels of redox regulators, membrane-bound globin chains, and cytoskeletal protein fragments in hereditary spherocytosis erythrocyte proteome
- Erythrocyte membrane protein defects in hereditary spherocytosis patients in Turkish population
- Erythroid Krüppel-Like Factor (KLF1): A Surprisingly Versatile Regulator of Erythroid Differentiation
- First experience with single incision laparoscopic surgery in Slovakia: concomitant cholecystectomy and splenectomy in an 11-year-old girl with hereditary spherocytosis
- G6PD-MutDB: a mutation and phenotype database of glucose-6-phosphate (G6PD) deficiency
- Glucose Phosphate Isomerase Deficiency: High Prevalence of p.Arg347His Mutation in Indian Population Associated with Severe Hereditary Non-Spherocytic Hemolytic Anemia Coupled with Neurological Dysfunction
- Haemolytic icterus (acholuric jaundice) congenital and acquired
- Hematological and molecular analysis of patients with G6PD deficiency revealed coexistent hereditary spherocytosis and alpha thalassemia
- Hereditary Elliptocytosis
- Hereditary Elliptocytosis
- Hereditary Non-Spherocytic Hemolytic Anemia (HNSHA): Four Children with Rare Hereditary Red Cell Enzymopathies
- Hereditary non-spherocytic hemolytic anemia and severe glucose phosphate isomerase deficiency in an Indian patient homozygous for the L487F mutation in the human GPI gene
- Hereditary spherocytic hemolytic anemia in an adult with the formation of ectopic foci of extramedullary hemopoiesis in the chest
- Hereditary spherocytosis
- Hereditary Spherocytosis - Diagnosis, Surgical Treatment and Outcomes. A Literature Review
- Hereditary spherocytosis diagnosed with extremely low glycated hemoglobin compared to plasma glucose levels
- Hypoplasia of the internal carotid artery: a rare cause of cerebral ischemic stroke in children
- Identification of new mutations in patients with hereditary spherocytosis by next-generation sequencing
- Increased red cell turnover in a line of CD22-deficient mice is caused by Gpi1c: a model for hereditary haemolytic anaemia
- Insane in the membrane: A case of hereditary spherocytic pyropoikilocytosis
- Mean reticulocyte volume enhances the utility of red cell mean sphered cell volume in differentiating peripheral blood spherocytes of hereditary spherocytosis from other causes
- Mild erythrocytosis as a presenting manifestation of <em>PIEZO1</em> associated erythrocyte volume disorders
- Molecular Analyses of Pyruvate Kinase Deficient Turkish Patients from a Single Center
- Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte
- Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p.Ala337Thr) novel mutation in GPI gene in two Indian patients
- Mutational Characteristics of Causative Genes in Chinese Hereditary Spherocytosis Patients: a Report on Fourteen Cases and a Review of the Literature
- New missense homozygous mutation (Q270Ter) in the pyrimidine 5' nucleotidase type I-related gene in two Indian families with hereditary non-spherocytic hemolytic anemia
- Novel alpha-spectrin mutation in trans with alpha-spectrin causing severe neonatal jaundice from hereditary spherocytosis
- Novel compound heterozygous mutations in the SPTA1 gene, causing hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice
- Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the <em>HK1</em> gene causing severe haemolytic anaemia with developmental delay in an Indian family
- Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the HK1 gene causing severe haemolytic anaemia with developmental delay in an Indian family
- Novel α-spectrin mutation in trans with α-spectrin causing severe neonatal jaundice from hereditary spherocytosis
- Phase Angle: Could Be an Easy Tool to Detect Low-Grade Systemic Inflammation in Adults Affected by Prader-Willi Syndrome?
- PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus
- Prolonged Exposure Therapy for Post-traumatic Stress Disorder
- Proteomic identification of erythrocyte membrane protein deficiency in hereditary spherocytosis
- Pyruvate kinase activator: A major breakthrough in the world of Hematology
- Pyruvate Kinase Deficiency
- Pyruvate Kinase Deficiency
- Rapid Identification of Biallelic <em>SPTB</em> Mutation in a Neonate with Severe Congenital Hemolytic Anemia and Liver Failure
- Rapid Identification of Biallelic SPTB Mutation in a Neonate with Severe Congenital Hemolytic Anemia and Liver Failure
- Red blood cell aquaporin-1 expression is decreased in hereditary spherocytosis
- Red Blood Cell Metabolism in Pyruvate Kinase Deficient Patients
- Red cell ektacytometry in two patients with chronic hemolytic anemia and three new alpha-spectrin variants
- Red cell ektacytometry in two patients with chronic hemolytic anemia and three new α-spectrin variants
- Red cell membrane disorders
- Red cell pyruvate kinase deficiency in Southern Sardinia
- Residual pyruvate kinase activity in PKLR-deficient erythroid precursors of a patient suffering from severe haemolytic anaemia
- Resistant anaemia; a note on the differential diagnosis of pernicious anaemia and familial acholuric jaundice
- SARS-CoV nucleocapsid protein interacts with cellular pyruvate kinase protein and inhibits its activity
- Screening and confirmation of hereditary spherocytosis in children using a CELL-DYN Sapphire haematology analyser
- Spherocytosis in Newborn Secondary to Novel Heterozygous Mutation in <em>SPTB</em> Gene: Case Report
- Splenectomy for hereditary spherocytosis: complete, partial or not at all?
- Targeted next-generation sequencing identifies a novel nonsense mutation in SPTB for hereditary spherocytosis: A case report of a Korean family
- Targeted next-generation sequencing identifies eighteen novel mutations expanding the molecular and clinical spectrum of PKLR gene disorders in the Indian population
- TGA/Chemometric Test Is Able to Detect the Presence of a Rare Hemoglobin Variant Hb Bibba
- The pyruvate kinase (PK) to hexokinase enzyme activity ratio and erythrocyte PK protein level in the diagnosis and phenotype of PK deficiency
- The variable manifestations of disease in pyruvate kinase deficiency and their management
- Tokyo-1 Mutation: Hereditary Spherocytosis in a Hispanic Newborn Presenting as Early Onset Severe Hyperbilirubinemia
- Two different pathogenic gene mutations coexisted in the same hereditary spherocytosis family manifested with heterogeneous phenotypes
- Utility of Cryohemolysis Test in the Diagnosis of Hereditary Spherocytosis
- Utility of mean sphered cell volume and mean reticulocyte volume for the diagnosis of hereditary spherocytosis
- Ventricular assist device implantation in a young patient with non-compaction cardiomyopathy and hereditary spherocytosis
- When HbA1c is unreliable : a case report of hereditary spherocytosis