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

Topics Community

Article

Too many numbers and complexity: time to update the classifications of neurogenetic disorders?

Journal of medical genetics - 1 Oct 2016

Vallat Jean-Michel, Goizet Cyril, Magy Laurent, Mathis Stéphane

Abstract excerpt

No abstract is available from the source.

Topics

Cerebellar Ataxia
Charcot-Marie-Tooth Disease
Genetic Predisposition to Disease
Humans
Mutation
Spastic Paraplegia, Hereditary
Terminology as Topic

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 26518709
DOI: 10.1136/jmedgenet-2015-103477

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Too many numbers and complexity: time to update the classifications of neurogenetic disorders?PMID 26518709Read ↗

Defining neurogenetic phenotypes (or how to compare needles in haystacks).Semantic proximity Read ↗

The Drastic Turn in Neurology: From Classical Disciplines to NeurogeneticsSemantic proximity Read ↗

Approaches to the patient with neurogenetic disease.Semantic proximity Read ↗

Neurofibromatosis: emerging phenotypes, mechanisms and management.Semantic proximity Read ↗

Mechanisms underlying phenotypic variation in neurogenetic disordersSemantic proximity Read ↗

Neurological diagnoses identify molecular processes.Semantic proximity Read ↗

What is complex about complex disorders?Semantic proximity Read ↗

Introduction to Neurogenetics.Semantic proximity Read ↗

Batten's disease: eight genes and still counting?Semantic proximity Read ↗

Neurogenetics II: complex disorders.Semantic proximity Read ↗

NIDDM enigma.Semantic proximity Read ↗

Phenotypes of the tuberous sclerosis complex with a revision of diagnostic criteria.Semantic proximity Read ↗

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