Different Saccadic Abnormalities in PINK1 Mutation Carriers and in Patients with Non-genetic Parkinson's Disease

Overview

Journal J Neurol

Specialty Neurology

Date 2009 Mar 31

PMID 19330279

Citations 5

Authors

Susanne Hertel

Andreas Sprenger

Christine Klein

Detlef Kompf

Christoph Helmchen

Hubert Kimmig

Affiliations

Soon will be listed here.

Citing Articles

Multimodal oculomotor assessment reveals prodromal markers of Parkinson's disease in non-manifesting LRRK2 G2019S mutation carriers.

Riek H, Visanji N, Pitigoi I, Di Luca D, Armengou-Garcia L, Ahmed N NPJ Parkinsons Dis. 2024; 10(1):234.

PMID: 39702611 PMC: 11659598. DOI: 10.1038/s41531-024-00840-w.

Oculomotor Dysfunction in Idiopathic and LRRK2-Parkinson's Disease and At-Risk Individuals.

Lage C, Sanchez-Rodriguez A, Rivera-Sanchez M, Sierra M, Gonzalez-Aramburu I, Madera J J Parkinsons Dis. 2024; 14(4):797-808.

PMID: 38701160 PMC: 11191487. DOI: 10.3233/JPD-230416.

Oculomotor abnormalities indicate early executive dysfunction in prodromal X-linked dystonia-parkinsonism (XDP).

Mertin R, Diesta C, Bruggemann N, Rosales R, Hanssen H, Westenberger A J Neurol. 2023; 270(9):4262-4275.

PMID: 37191726 PMC: 10421788. DOI: 10.1007/s00415-023-11761-8.

Eye Movements in Parkinson's Disease and Inherited Parkinsonian Syndromes.

Pretegiani E, Optican L Front Neurol. 2017; 8:592.

PMID: 29170650 PMC: 5684125. DOI: 10.3389/fneur.2017.00592.

Parkinson's disease and 2009: recent advances.

Breen D, Barker R J Neurol. 2010; 257(7):1224-8.

PMID: 20376474 DOI: 10.1007/s00415-010-5555-y.

References

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