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

Isolated palatal tremor as unique clinical manifestation of SCA 18 due to a new mutation of IFRD1.

Parkinsonism & related disorders - 1 Sept 2017

Echeveste Beatriz, Covarrubias Eva, Cabello Juan Pablo, Luquin María-Rosario

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 Immediate-Early Proteins
Share to Mutation
Share to Spinocerebellar Degenerations
Share to Tremor

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 28601596
DOI: 10.1016/j.parkreldis.2017.05.026

Genes

IFRD1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Isolated palatal tremor as unique clinical manifestation of SCA 18 due to a new mutation of IFRD1.PMID 28601596Read ↗

Palatal Tremor Revisited: Disorder with Nosological Diversity and Etiological Heterogeneity.Semantic proximity Read ↗

Teaching Video NeuroImages: Palatal tremor associated with SPG7 variants.Semantic proximity Read ↗

A novel ATP1A3 mutation with unique clinical presentation.Semantic proximity Read ↗

Isolated and combined genetic tremor syndromes: a critical appraisal based on the 2018 MDS criteria.Semantic proximity Read ↗

A novel CACNA1A mutation associated with adult-onset, paroxysmal head tremor.Semantic proximity Read ↗

Writing tremor: Should we look for a TOR1A mutation?Semantic proximity Read ↗

DNAJC6 mutation causing cranial-onset dystonia with tremor dominant levodopa non-responsive parkinsonism: A novel phenotype.Semantic proximity Read ↗

A novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood.Semantic proximity Read ↗

Paroxysmal tonic upgaze (PTU) associated with CACNA1A mutation and gross motor delay.Semantic proximity Read ↗

Long-term changes in electroencephalogram findings in a girl with a nonsense SMC1A variant: A case reportSemantic proximity Read ↗

Oromandibular and Laryngeal Dystonia Secondary to Dystonia 6 Due to THAP1 Variant in a Child.Semantic proximity Read ↗

Identification of FXTAS presenting with SCA 12 like phenotype in India.Semantic proximity Read ↗

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