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

Clinical features of parkinsonian patients with the alpha-synuclein (G209A) mutation.

Movement disorders : official journal of the Movement Disorder Society - 1 Nov 2001

Bostantjopoulou S, Katsarou Z, Papadimitriou A, Veletza V, Hatzigeorgiou G, Lees A

Abstract excerpt

The motor and neuropsychological abnormalities in eight Greek patients with Parkinson's disease (PD) carrying the alpha-synuclein gene mutation (G209A) were studied. These patients (five men, three women) belonged to six different families. Their symptoms started between 32-50 years of age (mean +/- SD, 39.7 +/- 7.6 years) and they had a mean disease duration of 5.4 +/- 2.1 years (range, 2-9 years) at the time of...

Read the complete abstract on PubMed

Topics

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

Share to alpha-Synuclein
Share to Cognition Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Diagnosis, Differential

Share to Greece

Share to Neuropsychological Tests

Share to Parkinson Disease

Share to Phosphoproteins

Share to Synucleins

Source

Identifiers

PMID: 11748731
DOI: 10.1002/mds.1221

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical features of parkinsonian patients with the alpha-synuclein (G209A) mutation.PMID 11748731Read ↗

Clinical characteristics of the alpha-synuclein mutation (G209A)-associated Parkinson's disease in comparison with other forms of familial Parkinson's disease in Greece.Semantic proximity Read ↗

Clinical phenotype in patients with alpha-synuclein Parkinson's disease living in Greece in comparison with patients with sporadic Parkinson's disease.Semantic proximity Read ↗

Dementia with Lewy bodies in an elderly Greek male due to alpha-synuclein gene mutation.Semantic proximity Read ↗

Disease-related and genetic correlates of psychotic symptoms in Parkinson's disease.Semantic proximity Read ↗

Clinical and pathological features of a Parkinsonian syndrome in a family with an Ala53Thr alpha-synuclein mutation.Semantic proximity Read ↗

The G209A mutation in the alpha-synuclein gene in Brazilian families with Parkinson's disease.Semantic proximity Read ↗

Motor and Nonmotor Features of Carriers of the p.A53T Alpha-Synuclein Mutation: A Longitudinal Study.Semantic proximity Read ↗

Mutated alpha-synuclein gene in two Greek kindreds with familial PD: incomplete penetrance?Semantic proximity Read ↗

Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene.Semantic proximity Read ↗

LRRK2 G2019S mutation in Parkinson's disease: a neuropsychological and neuropsychiatric study in a large Algerian cohort.Semantic proximity Read ↗

Analysis of the α-synuclein G209A mutation in familial Parkinson's diseaseSemantic proximity Read ↗

Absence of the G209A mutation in the alpha-synuclein gene in British families with Parkinson's disease.Semantic proximity Read ↗

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