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

Fetal-neonatal alloimmune thrombocytopenia and unexpected Glanzmann thrombasthenia carrier: report of two cases.

Transfusion - 1 Apr 2005

Jallu Vincent, Bianchi Frédéric, Kaplan Cécile

Abstract excerpt

BACKGROUND: Discrepancy between phenotyping and genotyping during the investigation of maternofetal alloimmunization leads to the identification of defects on genes encoding membrane glycoproteins (GPs) IIb and IIIa. STUDY DESIGN AND METHODS: Human platelet (PLT) alloantigen (HPA)-1 and -3 PLT phenotypes and genotypes were performed by use of, respectively, the monoclonal antibody-specific immobilization of PLT...

Read the complete abstract on PubMed

Topics

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

Share to Antigens, Human Platelet
Share to Diagnostic Errors
Share to Erythroblastosis, Fetal

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

Share to Point Mutation

Share to Pregnancy

Share to Pregnancy Complications, Hematologic

Share to Thrombasthenia

Share to Thrombocytopenia

Source

Identifiers

PMID: 15819676
DOI: 10.1111/j.0041-1132.2005.04275.x

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Fetal-neonatal alloimmune thrombocytopenia and unexpected Glanzmann thrombasthenia carrier: report of two cases.PMID 15819676Read ↗

Immunization against a low-frequency human platelet alloantigen in fetal alloimmune thrombocytopenia is not a single event: characterization by the combined use of reference DNA and novel allele-specific cell lines expressing recombinant antigens.Semantic proximity Read ↗

New platelet glycoprotein polymorphisms causing maternal immunization and neonatal alloimmune thrombocytopenia.Semantic proximity Read ↗

Severe fetomaternal alloimmune thrombocytopenia due to anti-human platelet antigen (HPA)-1a in a mother with a rare and silenced ITGB3*0101 (GPIIIa) allele.Semantic proximity Read ↗

A V740L mutation in glycoprotein IIb defines a novel epitope (War) associated with fetomaternal alloimmune thrombocytopenia.Semantic proximity Read ↗

New K103 β3 allele identified in a context of severe neonatal thrombocytopenia.Semantic proximity Read ↗

HPA-5 typing discrepancy reveals an Ile503Leu substitution in platelet GPIa (α2 integrin).Semantic proximity Read ↗

HPA-13bw neonatal alloimmune thrombocytopenia and low frequency alloantigens: case report and review of the literature.Semantic proximity Read ↗

Neonatal alloimmune thrombocytopenia: current considerations.Semantic proximity Read ↗

Alloantibodies against low-frequency human platelet antigens do not account for a significant proportion of cases of fetomaternal alloimmune thrombocytopenia: evidence from 1054 cases.Semantic proximity Read ↗

Compound heterozygosity of HLA-DRB3*01:01 and HLA-DRB4*01:01 as a potential predictor of fetal neonatal alloimmune thrombocytopenia.Semantic proximity Read ↗

Maternal alloimmunization against the rare platelet‐specific antigen HPA‐9b (Max<sup>a</sup>) is an important cause of neonatal alloimmune thrombocytopeniaSemantic proximity Read ↗

A nait-associated and previously unreported mutation in the ITGB3 gene with a low frequency in the local population.Semantic proximity Read ↗

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