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

Why factor XI deficiency is a clinical concern.

Expert review of hematology - 1 Jul 2016

Wheeler Allison P, Gailani David

Abstract excerpt

INTRODUCTION: Inherited fXI deficiency has been an enigma since its discovery in 1953. The variable and relatively mild symptoms in patients with even the most severe form of the disorder seem out of step with the marked abnormalities in standard clotting assays. Indeed, the contribution of factor XI to hemostasis in an individual is not adequately assessed by techniques available in modern clinical laboratories....

Read the complete abstract on PubMed

Topics

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

Share to Blood Coagulation
Share to Blood Coagulation Tests
Share to Factor XI

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Factor XI Deficiency

Share to Genetic Association Studies

Share to Hemorrhage

Share to Phenotype

Source

Open in PubMed Open full text

Identifiers

PMID: 27216469
DOI: 10.1080/17474086.2016.1191944
PMCID: PMC4950943

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

Why factor XI deficiency is a clinical concern.PMID 27216469Read ↗

How to Capture the Bleeding Phenotype in FXI-Deficient Patients.Semantic proximity Read ↗

Factor XIII deficiency: an update.Semantic proximity Read ↗

Rare bleeding disorders - bleeding assessment tools, laboratory aspects and phenotype and therapy of FXI deficiency.Semantic proximity Read ↗

Clinical characteristics and genetic variant spectrum of 27 patients with coagulation factor XI deficiency.Semantic proximity Read ↗

Factor XIII Deficiency: Laboratory, Molecular, and Clinical AspectsSemantic proximity Read ↗

The History of Factor XIII Deficiency.Semantic proximity Read ↗

Clinical manifestations and mutation spectrum of 57 subjects with congenital factor XI deficiency in China.Semantic proximity Read ↗

Factor XI deficiency--from molecular genetics to clinical management.Semantic proximity Read ↗

Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited and acquired forms.Semantic proximity Read ↗

Congenital factor XI deficiency: an update.Semantic proximity Read ↗

Biological determinants of bleeding in patients with heterozygous factor XI deficiency.Semantic proximity Read ↗

Characterization of hereditary factor XI deficiency in Taiwanese patients: identification of three novel and two common mutations.Semantic proximity Read ↗

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