Olfactory identification in LRRK2 G2019S mutation carriers: a relevant marker?

OBJECTIVE: Olfactory impairment is a potential marker for impending phenoconversion to Parkinson disease (PD) that may precede the development of disease by several years. Because of low specificity, it may be of greater predictive value in those with genetic mutations and its potential as a marker...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Ann Clin Transl Neurol
Päätekijät: Saunders-Pullman, Rachel, Mirelman, Anat, Wang, Cuiling, Alcalay, Roy N, San Luciano, Marta, Ortega, Robert, Raymond, Deborah, Mejia-Santana, Helen, Ozelius, Laurie, Clark, Lorraine, Orr-Utreger, Avi, Marder, Karen, Giladi, Nir, Bressman, Susan B
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BlackWell Publishing Ltd 2014
Aiheet:
Research Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4241794/
https://ncbi.nlm.nih.gov/pubmed/25493281
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.95
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