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

Charcot–Marie–Tooth diseases: an update and some new proposals for the classification

5 Aug 2015

Abstract excerpt

BACKGROUND: Charcot-Marie-Tooth (CMT) disease, the most frequent form of inherited neuropathy, is a genetically heterogeneous group of disorders of the peripheral nervous system, but with a quite homogeneous clinical phenotype (progressive distal muscle weakness and atrophy, foot deformities, distal sensory loss and usually decreased tendon reflexes). Our aim was to review the various CMT subtypes identified at...

Read the complete abstract on PubMed

Topics

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

Share to Hereditary Neurological Disorders
Share to Peripheral Neuropathies and Disorders

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 26246519
DOI: 10.1136/jmedgenet-2015-103272

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 · 12 closest

Charcot–Marie–Tooth diseases: an update and some new proposals for the classificationPMID 26246519Read ↗

[Charcot-Marie-Tooth (CMT) disease: an update].Semantic proximity Read ↗

Charcot‐Marie‐Tooth Disease: A Clinico‐genetic ConfrontationSemantic proximity Read ↗

Update on Charcot-Marie-Tooth disease.Semantic proximity Read ↗

The shifting paradigm of Charcot-Marie-Tooth disease.Semantic proximity Read ↗

Charcot-Marie-tooth disease.Semantic proximity Read ↗

Clinical practice guidelines for the diagnosis and management of Charcot-Marie-Tooth diseaseSemantic proximity Read ↗

[Hereditary motor-sensory neuropathies (Charcot-Marie-Tooth syndrome) and related neuropathies. Current classification and genotype-phenotype correlation].Semantic proximity Read ↗

The various Charcot-Marie-Tooth diseases.Semantic proximity Read ↗

Charcot-Marie-Tooth neuropathies: diagnosis and management.Semantic proximity Read ↗

Genetics of Charcot-Marie-Tooth disease type 4A: mutations, inheritance, phenotypic variability, and founder effectSemantic proximity Read ↗

Charcot–Marie–Tooth disease and related disorders: an evolving landscapeSemantic proximity Read ↗

[Guidelines for molecular diagnosis of Charcot-Marie-Tooth disease].Semantic proximity Read ↗

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