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

Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathy.

Muscle & nerve - 1 Dec 1998

Pareyson D, Solari A, Taroni F, Botti S, Fallica E, Scaioli V, Ciano C, Sghirlanzoni A

Abstract excerpt

Hereditary neuropathy with liability to pressure palsies (HNPP) is an autosomal dominant disorder characterized by recurrent mononeuropathies or brachial plexopathies, commonly associated with a chromosome 17p11.2-12 deletion encompassing the peripheral myelin protein-22 (PMP22) gene. We tried to identify criteria distinguishing HNPP among patients with acute painless mononeuropathy/plexopathy. We investigated by...

Read the complete abstract on PubMed

Topics

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

Share to Acute Disease
Share to Adolescent

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

Share to Diagnosis, Differential

Share to Electrophoresis, Gel, Pulsed-Field

Share to Gene Deletion

Share to Genetic Predisposition to Disease

Share to Nervous System Diseases

Source

Identifiers

PMID: 9843070
DOI: 10.1002/(sici)1097-4598(199812)21:12<1686::aid-mus10>3.0.co;2-z

Genes

PMP22

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

Detection of hereditary neuropathy with liability to pressure palsies among patients with acute painless mononeuropathy or plexopathy.PMID 9843070Read ↗

Hereditary neuropathy with liability to pressure palsies: description of seven patients without known family history.Semantic proximity Read ↗

Hereditary neuropathy with liability to pressure palsy: a brief review with a case report.Semantic proximity Read ↗

Recurrent brachial plexus palsies as the only clinical expression of hereditary neuropathy with liability to pressure palsies associated with a de novo deletion of the peripheral myelin protein-22 gene.Semantic proximity Read ↗

Loss-of-function phenotype of hereditary neuropathy with liability to pressure palsies.Semantic proximity Read ↗

Hereditary neuropathy with liability to pressure palsy: two cases of difficult diagnosis.Semantic proximity Read ↗

Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion.Semantic proximity Read ↗

Recurrent polyradiculoneuropathy with the 17p11.2 deletion.Semantic proximity Read ↗

[Hereditary neuropathy with liability to pressure palsies in childhood: Report of three cases].Semantic proximity Read ↗

Electrodiagnostic Characterization of Hereditary Neuropathy With Liability to Pressure Palsies.Semantic proximity Read ↗

Clinical, electrophysiological and magnetic resonance findings in a family with hereditary neuropathy with liability to pressure palsies caused by a novel PMP22 mutation.Semantic proximity Read ↗

Hereditary neuropathy with liability to pressure palsy (HNPP): report of a family with a new point mutation in PMP22 gene.Semantic proximity Read ↗

Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy.Semantic proximity Read ↗

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