Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Polycythemia revealing PIEZO1 hereditary xerocytosis.

Blood - 4 Jul 2024

Cordeil Stephanie, Jallades Laurent

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Anemia, Hemolytic, Congenital
Share to Hydrops Fetalis
Share to Ion Channels
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polycythemia

Source

Identifiers

PMID: 38963666
DOI: 10.1182/blood.2024024199

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Polycythemia revealing PIEZO1 hereditary xerocytosis.PMID 38963666Read ↗

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

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

Increased incidence of germline PIEZO1 mutations in individuals with idiopathic erythrocytosisSemantic proximity Read ↗

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

Non-immune hydrops fetalis caused by PIEZO1 compound heterozygous deletions detected only by exome sequencing.Semantic proximity Read ↗

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

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

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

PIEZO1 Hypomorphic Variants in Congenital Lymphatic Dysplasia Cause Shape and Hydration Alterations of Red Blood CellsSemantic proximity Read ↗

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

⌁Select a neighboring publication to make it the new centre.