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

Sensory-motor not length-dependent multineuropathy followed by the syringomyelia-like phenotype: a novel presentation of Tangier disease.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology - 1 Dec 2022

Sabatelli Eleonora, Luigetti Marco, Costantini Umberto, Lucioli Gabriele, Conte Amelia

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 Magnetic Resonance Imaging
Share to Phenotype
Share to Tangier Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 35960386
DOI: 10.1007/s10072-022-06334-y

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Sensory-motor not length-dependent multineuropathy followed by the syringomyelia-like phenotype: a novel presentation of Tangier disease.PMID 35960386Read ↗

Tangier disease with unusual clinical manifestations.Semantic proximity Read ↗

Sensory-motor neuropathy in a case with SPG35: Expanding the phenotype.Semantic proximity Read ↗

A novel nonsense mutation in the ABC1 gene causes a severe syringomyelia-like phenotype of Tangier disease.Semantic proximity Read ↗

The neuropathy in hereditary transthyretin amyloidosis: A narrative review.Semantic proximity Read ↗

X-linked dystonia ("Lubag") presenting predominantly with parkinsonism: a more benign phenotype?Semantic proximity Read ↗

An unusual phenotype of McLeod syndrome with late onset axonal neuropathy.Semantic proximity Read ↗

Hereditary motor sensory neuropathy (type 1) presenting with transient and persistent central nervous system manifestations: a novel genetic mutation.Semantic proximity Read ↗

A novel mutation in the ABCA1 gene causing an atypical phenotype of Tangier disease.Semantic proximity Read ↗

Tangier DiseaseSemantic proximity Read ↗

Giant axonal neuropathy: An updated perspective on its pathology and pathogenesis.Semantic proximity Read ↗

ATP1A3 related disease manifesting as rapid onset dystonia-parkinsonism with prominent myoclonus and exaggerated startle.Semantic proximity Read ↗

A novel familial prion disease causing pan‐autonomic‐sensory neuropathy and cognitive impairmentSemantic proximity Read ↗

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