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

Laryngeal neuropathy of Charcot-Marie-Tooth disease: further observations and novel mutations associated with vocal fold paresis.

The Laryngoscope - 1 Feb 2010

Benson Brian, Sulica Lucian, Guss Joel, Blitzer Andrew

Abstract excerpt

OBJECTIVES/HYPOTHESIS: To describe and define laryngeal neuropathy in Charcot-Marie-Tooth (CMT) disease. STUDY DESIGN/METHODS: Retrospective record review from a university laryngology practice. RESULTS: Four adult CMT patients presented with laryngeal symptoms. Three patients exhibited bilateral...

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 Electromyography
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 19950375
DOI: 10.1002/lary.20685

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19950375-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 10 closest

Laryngeal neuropathy of Charcot-Marie-Tooth disease: further observations and novel mutations associated with vocal fold paresis.PMID 19950375Read ↗

Charcot-Marie-Tooth disease: A case report initially manifested by bilateral vocal cord paralysisSemantic proximity Read ↗

Mutational screening of GDAP1 in dysphonia associated with Charcot-Marie-Tooth disease: clinical insights and phenotypic effectsSemantic proximity Read ↗

Vocal cord paresis and diaphragmatic dysfunction are severe and frequent symptoms of GDAP1-associated neuropathy.Semantic proximity Read ↗

Vocal cord paralysis in Charcot-Marie-Tooth type 4b1 disease associated with a novel mutation in the myotubularin-related protein 2 gene: A case report and review of the literature.Semantic proximity Read ↗

CMT2C with vocal cord paresis associated with short stature and mutations in the TRPV4 gene.Semantic proximity Read ↗

Phenomenology, genetics, and CNS network abnormalities in laryngeal dystonia: A 30-year experience.Semantic proximity Read ↗

Multiple Symmetric Lipomatosis (Madelung Disease) in a Large Canadian Family With the Mitochondrial MTTK c.8344A>G VariantSemantic proximity Read ↗

Beyond cervical lipomas: myoclonus, gait disorder and multisystem involvement leading to mitochondrial disease.Semantic proximity Read ↗

Clinical, electrophysiological and morphological findings of Charcot-Marie-Tooth neuropathy with vocal cord palsy and mutations in the GDAP1 gene.Semantic proximity Read ↗

Multiple lipomas, alcoholism, and neuropathy: Madelung's disease or MERRF?Semantic proximity Read ↗

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