ReviewPediatric clinics of North America2013
Abnormalities of the erythrocyte membrane.
Review in Pediatric clinics of North America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.
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Who cites it
40 citing papers in PubMed.
- Hereditary Elliptocytosis Identified During the Evaluation of Splenomegaly: A Case Report.Cureus · 2026Article
- Article
- Iron deficiency anemia perturbs erythrocyte morphology and may promote eryptosis.International journal of hematology · 2026Article
- Crossed Erythrocytes Agglutination Pattern Observed in a Patient With Hereditary Elliptocytosis.International journal of laboratory hematology · 2026Article
- Main events and mechanism of human erythrocyte ageing.Expert reviews in molecular medicine · 2026Review
- Hereditary Spherocytosis: Linking Ion Transport Defects to Osmotic Gradient Ektacytometry Profiles-A Review.International journal of molecular sciences · 2026Review
- Expanding the genetic landscape ofFrontiers in genetics · 2026Article
- Severe Hereditary Pyropoikilocytosis/Hereditary Elliptocytosis-Like Phenotype Associated With a HeterozygousCase reports in hematology · 2026Article
- Understanding the genetic architecture and phenotypic landscape of SPTB gene variants causing hereditary spherocytosis in an Indian cohort.Human genetics · 2025Article
- Biomechanics of phagocytosis of red blood cells by macrophages in the human spleen.Proceedings of the National Academy of Sciences of the United States of America · 2024Article
- Nanoscale dynamics of actin filaments in the red blood cell membrane skeleton.Molecular biology of the cell · 2022Article
- Haemolytic anemia triggered by SARS-CoV-2 in patient with hereditary spherocytosis.Medicina clinica (English ed.) · 2021Article
- Haemolytic anemia triggered by SARS-CoV-2 in patient with hereditary spherocytosis.Medicina clinica · 2021Article
- Article
- A novel essential splice site variant in SPTB in a large hereditary spherocytosis family.Molecular genetics & genomic medicine · 2021Article
- Identification of a De Novoc.1000delA ANK1 mutation associated to hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice-case reports and review of the literature.BMC medical genomics · 2021Review
- Review
- Aberrant Membrane Composition and Biophysical Properties Impair Erythrocyte Morphology and Functionality in Elliptocytosis.Biomolecules · 2020Article
- Exome sequencing for diagnosis of congenital hemolytic anemia.Orphanet journal of rare diseases · 2020Article
- Red cell membrane protein abnormalities as defined by sds-page among patients with anemia in a West African region hospital practice.Caspian journal of internal medicine · 2020Article
Corrections and comments
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Authors and funding
1 author.
Funding
Abstract
Primary abnormalities of the erythrocyte membrane are characterized by clinical, laboratory, and genetic heterogeneity. Among this group, hereditary spherocytosis patients are more likely to experience symptomatic anemia. Treatment of hereditary spherocytosis with splenectomy is curative in most patients. Growing recognition of the long-term risks of splenectomy has led to re-evaluation of the role of splenectomy. Management guidelines acknowledge these considerations and recommend discussion between health care providers, patient, and family. The hereditary elliptocytosis syndromes are the most common primary disorders of erythrocyte membrane proteins. However, most elliptocytosis patients are asymptomatic and do not require therapy.
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