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Hereditary xerocytosis and familial haemolysis due to mutation in the PIEZO1 gene: a simple diagnostic approach.

International journal of laboratory hematology - 1 Aug 2014

Sandberg M B, Nybo M, Birgens H, Frederiksen H

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Topics

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Anemia, Hemolytic, Congenital
Erythrocytes
Hemolysis
Hydrops Fetalis
Ion Channels
Ion Transport
Potassium

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 24314002
DOI: 10.1111/ijlh.12172

Genes

PIEZO1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

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Hereditary xerocytosis and familial haemolysis due to mutation in the PIEZO1 gene: a simple diagnostic approach.PMID 24314002Read ↗

Polycythemia revealing PIEZO1 hereditary xerocytosis.Semantic proximity Read ↗

Hereditary red blood cell membrane defects. Detection of PIEZO1 mutations associated with SPTA1 mutations. An unusual clinical case of hereditary xerocytosis.Semantic proximity Read ↗

Recent advances in the pathophysiology of PIEZO1 ‐related hereditary xerocytosisSemantic proximity Read ↗

Hereditary xerocytosis - spectrum and clinical manifestations of variants in the PIEZO1 gene, including co-occurrence with a novel β-globin mutation.Semantic proximity Read ↗

Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis.Semantic proximity Read ↗

Recurrent mutation in the PIEZO1 gene in two families of hereditary xerocytosis with fetal hydrops.Semantic proximity Read ↗

PIEZO1-related Hereditary Xerocytosis in a boy with cardiac arrhythmiaSemantic proximity Read ↗

New insights on hereditary erythrocyte membrane defectsSemantic proximity Read ↗

A novel PIEZO1 mutation in a patient with dehydrated hereditary stomatocytosis: a case report and a brief review of literatureSemantic proximity Read ↗

Complex Modes of Inheritance in Hereditary Red Blood Cell Disorders: A Case Series Study of 155 Patients.Semantic proximity Read ↗

Impaired PIEZO1 function in patients with a novel autosomal recessive congenital lymphatic dysplasia.Semantic proximity Read ↗

Proteome alterations in erythrocytes with PIEZO1 gain-of-function mutations.Semantic proximity Read ↗

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