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

Hydrops fetalis associated with erythrocyte pyruvate kinase deficiency

9 Jun 2000

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 Blood properties and coagulation
Share to Erythrocyte Function and Pathophysiology
Share to Parvovirus B19 Infection Studies

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 10923218
DOI: 10.1007/s004310051314

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hydrops fetalis associated with erythrocyte pyruvate kinase deficiencyPMID 10923218Read ↗

Hematologically important mutations: red cell pyruvate kinase.Semantic proximity Read ↗

Red blood cell PK deficiency: An update of PK-LR gene mutation database.Semantic proximity Read ↗

The variable manifestations of disease in pyruvate kinase deficiency and their managementSemantic proximity Read ↗

[From gene to disease; hereditary non-spherocytic hemolytic anemia caused by pyruvate kinase deficiency].Semantic proximity Read ↗

Red cell pyruvate kinase deficiency: from genetics to clinical manifestations.Semantic proximity Read ↗

Genotype‐phenotype correlation and molecular heterogeneity in pyruvate kinase deficiencySemantic proximity Read ↗

Red cell glycolytic enzyme disorders caused by mutations: an update.Semantic proximity Read ↗

Six previously undescribed pyruvate kinase mutations causing enzyme deficiency.Semantic proximity Read ↗

Gene symbol: PKLR. Disease: Pyruvate kinase deficiency.Semantic proximity Read ↗

First reported case of prenatal diagnosis for pyruvate kinase deficiency in a Chinese family.Semantic proximity Read ↗

Pyruvate kinase deficiency: the genotype-phenotype association.Semantic proximity Read ↗

Pyruvate kinase deficiency in France: a 3-year study reveals 27 new mutations.Semantic proximity Read ↗

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