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

Variable bleeding phenotype in an Amish pedigree with von Willebrand disease.

American journal of hematology - 1 Oct 2016

Gupta Sweta, Heiman Meadow, Duncan Natalie, Hinckley Jesse, Di Paola Jorge, Shapiro Amy D

Abstract excerpt

Through a cross-sectional study design, the bleeding phenotype in the Amish in Indiana (IN) and Wisconsin (WI) was described using two different bleeding scores. von Willebrand factor (VWF) testing was performed and bleeding questionnaires from Centers for Disease Control and Prevention (CDC) and European MCMDM-1 (Tosetto bleeding score (BS)) were administered to the IN and WI cohort respectively. Seven hundred...

Read the complete abstract on PubMed

Topics

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

Share to Age Factors
Share to Cross-Sectional Studies
Share to Hemorrhage

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Point Mutation

Share to Sex Factors

Share to Surveys and Questionnaires

Share to von Willebrand Diseases

Share to Wisconsin

Source

Open in PubMed Open full text

Identifiers

PMID: 27414491
DOI: 10.1002/ajh.24474
PMCID: PMC5031525

Genes

VWF

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Variable bleeding phenotype in an Amish pedigree with von Willebrand disease.PMID 27414491Read ↗

Von Willebrand disease: classification and epidemiology.Semantic proximity Read ↗

Determinants of bleeding phenotype in adult patients with moderate or severe von Willebrand disease.Semantic proximity Read ↗

Congenital von Willebrand disease type I: definition, phenotypes, clinical and laboratory assessment.Semantic proximity Read ↗

Von willebrand disease: An overviewSemantic proximity Read ↗

[Von Willebrand disease : diagnosis and management].Semantic proximity Read ↗

Genetic determinants of clinical variability in type 2 von Willebrand disease: bridging genotype and phenotype.Semantic proximity Read ↗

Determinants of bleeding severity in von Willebrand disease.Semantic proximity Read ↗

Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States.Semantic proximity Read ↗

von Willebrand factor: the complex molecular genetics of a multidomain and multifunctional protein.Semantic proximity Read ↗

Von Willebrand disease in the United States: a perspective from Wisconsin.Semantic proximity Read ↗

Global Prevalence and Ethnic Diversity of von Willebrand Disease: An Updated Population-Based Genetic AnalysisSemantic proximity Read ↗

Variability in bleeding phenotype in Amish carriers of haemophilia B with the 31008 C-->T mutation.Semantic proximity Read ↗

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