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

Benign tremulous parkinsonism in a patient with dardarin mutation.

Movement disorders : official journal of the Movement Disorder Society - 15 Jul 2009

Rizzo Giovanni, Marconi Sara, Capellari Sabina, Scaglione Cesa, Martinelli Paolo

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 Aged, 80 and over
Share to Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
Share to Mutation
Share to Parkinson Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Protein Serine-Threonine Kinases

Share to Tremor

Source

Identifiers

PMID: 19373934
DOI: 10.1002/mds.22544

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

Benign tremulous parkinsonism in a patient with dardarin mutation.PMID 19373934Read ↗

A common LRRK2 mutation in idiopathic Parkinson's diseaseSemantic proximity Read ↗

Pure Parkinsonism as Possible Phenotype Expansion of THAP1-Related Disorders.Semantic proximity Read ↗

Parkinsonism in a patient with valosin-containing protein gene mutation showing: a case report.Semantic proximity Read ↗

How much does dardarin contribute to Parkinson's disease?Semantic proximity Read ↗

LRRK2 mutations in a clinic-based cohort of Parkinson's disease.Semantic proximity Read ↗

Diagnostic delay in Parkinson's disease caused by PRKN mutationsSemantic proximity Read ↗

The dardarin G 2019 S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases.Semantic proximity Read ↗

G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort.Semantic proximity Read ↗

Early-onset levodopa responsive parkinsonism in PPP2R5D mutation.Semantic proximity Read ↗

Novel ATP2A2 mutation in a patient with Darier's disease.Semantic proximity Read ↗

Rapidly progressive primary progressive aphasia and parkinsonism with novel GRN mutation.Semantic proximity Read ↗

Darier's Disease Complicated by Schizophrenia Caused by a Novel ATP2A2 Mutation.Semantic proximity Read ↗

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