Raynaud's phenomenon associated with Fabry disease.

doi:10.1007/s10545-014-9799-z

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

Community

Back to search

Article

Raynaud's phenomenon associated with Fabry disease.

Journal of inherited metabolic disease - 1 Mar 2015

Germain Dominique P, Atanasiu Oana I, Akrout-Marouene Jouda, Benistan Karelle

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 alpha-Galactosidase
Share to Fabry Disease
Share to Genetic Predisposition to Disease
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Phenotype

Share to Risk Factors

Source

Open in PubMed

Identifiers

PMID: 25511234
DOI: 10.1007/s10545-014-9799-z

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 9 closest

Raynaud's phenomenon associated with Fabry disease.PMID 25511234Read ↗

[Fabry disease: Pathogenesis, pathophysiology, and therapy].Semantic proximity Read ↗

Fabry disease previously diagnosed as Henoch-Schonlein purpura.Semantic proximity Read ↗

Anderson-Fabry disease.Semantic proximity Read ↗

The heart in Fabry's diseaseSemantic proximity Read ↗

A new phenotype of Fabry disease with intermediate severity between the classical form and the cardiac variant.Semantic proximity Read ↗

CMR demonstration of multiple morphological phenotypes in Anderson-Fabry diseaseSemantic proximity Read ↗

[Ophthalmological findings in a female patient with classical Fabry disease].Semantic proximity Read ↗

The frequency of Raynaud’s phenomenon in patients with methylenetetrahydrofolate reductase gene mutation and hyperhomocysteinemiaSemantic proximity Read ↗

Correlation of X chromosome inactivation with clinical presentation of Fabry disease in a case report.Semantic proximity Read ↗

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