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

Evaluation of platelet surface glycoproteins in patients with Glanzmann thrombasthenia: Association with bleeding symptoms.

The Indian journal of medical research - 1 May 2017

Mutreja Deepti, Sharma Rahul Kumar, Purohit Abhishek, Aggarwal Mukul, Saxena Renu

Abstract excerpt

BACKGROUND & OBJECTIVES: Glanzmann thrombasthenia (GT) is a rare, inherited autosomal recessive disorder characterized by qualitative or quantitative deficiency of integrin αIIbβ3 [glycoprotein IIb (GPIIb)/IIIa, CD41/CD61] diagnosed by absent or reduced platelet aggregation to physiological agonists, namely, collagen, adenosine-di-phosphate, epinephrine and arachidonic acid. The objective of this study was to...

Read the complete abstract on PubMed

Topics

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

Share to Blood Platelets
Share to Flow Cytometry

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glycoproteins

Share to Hemorrhage

Share to Integrin beta3

Share to Platelet Aggregation

Share to Platelet Glycoprotein GPIb-IX Complex

Share to Thrombasthenia

Source

Open in PubMed Open full text

Identifiers

PMID: 28948953
DOI: 10.4103/ijmr.IJMR_718_14
PMCID: PMC5644297

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Evaluation of platelet surface glycoproteins in patients with Glanzmann thrombasthenia: Association with bleeding symptoms.PMID 28948953Read ↗

Flow cytometric analysis of platelet surface glycoproteins in the diagnosis of thirty-two Turkish patients with Glanzmann thrombasthenia: a multicenter experienceSemantic proximity Read ↗

Glanzmann's Thrombasthenia: An OverviewSemantic proximity Read ↗

Profiling the Genetic and Molecular Characteristics of Glanzmann Thrombasthenia: Can It Guide Current and Future Therapies?Semantic proximity Read ↗

Glanzmann thrombasthenia: a review of ITGA2B and ITGB3 defects with emphasis on variants, phenotypic variability, and mouse models.Semantic proximity Read ↗

Glanzmann thrombasthenia: state of the art and future directions.Semantic proximity Read ↗

Inherited platelet disorders.Semantic proximity Read ↗

Molecular defects in ITGA2B and ITGB3 genes in patients with Glanzmann thrombasthenia.Semantic proximity Read ↗

Homozygous point mutations in platelet glycoprotein ITGA2B gene as cause of Glanzmann thrombasthenia in 2 families.Semantic proximity Read ↗

Should studies on Glanzmann thrombasthenia not be telling us more about cardiovascular disease and other major illnesses?Semantic proximity Read ↗

Inherited Platelet Function Disorders (IPFDs).Semantic proximity Read ↗

Understanding the genetic basis of Glanzmann thrombasthenia: implications for treatment.Semantic proximity Read ↗

Characterisation of patients with Glanzmann thrombasthenia and identification of 17 novel mutations.Semantic proximity Read ↗

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