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

Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsies.

Muscle & nerve - 1 Aug 2001

Ørstavik K, Skard Heier M, Young P, Stögbauer F

Abstract excerpt

Hereditary neuropathy with liability to pressure palsies (HNPP) is an autosomal-dominant focal neuropathy characterized by recurrent entrapment neuropathies. Single members of families with HNPP and brachial plexus involvement have been reported previously. We describe a family with three affected members and in which the only symptom of entrapment was recurrent brachial plexopathy. The diagnosis of HNPP in this...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 17
Share to DNA Mutational Analysis

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

Share to Electrodiagnosis

Share to Electromyography

Share to Genes, Dominant

Share to Loss of Heterozygosity

Share to Myelin Proteins

Share to Neural Conduction

Source

Identifiers

PMID: 11439387
DOI: 10.1002/mus.1116

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

Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsies.PMID 11439387Read ↗

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 ↗

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

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

Hereditary neuropathy with liability to pressure palsies: the same molecular defect can result in diverse clinical presentation.Semantic proximity Read ↗

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

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

Hereditary recurrent focal neuropathies: clinical and molecular features.Semantic proximity Read ↗

[Hereditary neural amyotrophy (HNA): clinical and molecular genetic basis].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 ↗

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

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

Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities.Semantic proximity Read ↗

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