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

Teaching NeuroImages: MR neurography for the diagnosis of hypertrophic neuropathies.

Neurology - 17 Oct 2017

Souza Paulo Victor Sgobbi de, Bortholin Thiago, Naylor Fernando George Monteiro, Pinto Wladimir Bocca Vieira de Rezende, Oliveira Acary Souza Bulle

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 Charcot-Marie-Tooth Disease
Share to Hypertrophy
Share to Magnetic Resonance Imaging
Share to Mutation

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

Source

Identifiers

PMID: 29038142
DOI: 10.1212/WNL.0000000000004525

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 17 Oct 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

Teaching NeuroImages: MR neurography for the diagnosis of hypertrophic neuropathies.PMID 29038142Read ↗

Teaching NeuroImages: characteristic phenotype of Ullrich congenital muscular dystrophy.Semantic proximity Read ↗

Teaching NeuroImages: hypertrophic olivary degeneration in a young man with POLG gene mutation.Semantic proximity Read ↗

Teaching NeuroImages: Hemiatrophy as a clinical presentation in facioscapulohumeral muscular dystrophy.Semantic proximity Read ↗

Teaching NeuroImages: Hypomyelinating leukodystrophy with generalized dystonia.Semantic proximity Read ↗

Teaching NeuroImages: neuroferritinopathy.Semantic proximity Read ↗

Teaching NeuroImages: Imaging phenotype of myoclonic epilepsy with ragged-red fibers.Semantic proximity Read ↗

Teaching NeuroImages: Adult-onset vanishing white matter disease.Semantic proximity Read ↗

Teaching NeuroImages: Slowly progressive hypertrophic brachial plexopathy due to SEPT9 mutation.Semantic proximity Read ↗

Teaching NeuroImages: Subacute encephalopathy in a young woman with THTR2 gene mutation.Semantic proximity Read ↗

Teaching NeuroImages: Spinocerebellar ataxia type 3 presenting with a cock-walk gait phenotype.Semantic proximity Read ↗

Teaching NeuroImages: Transient cytotoxic edema in a child with a novel ATP1A2 mutation.Semantic proximity Read ↗

Teaching NeuroImages: gelsolin-related amyloidosis: a rare cause of progressive facial diparesis.Semantic proximity Read ↗

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