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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...

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Détails bibliographiques
Publié dans:Ann Clin Transl Neurol
Auteurs principaux: 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
Format: Artigo
Langue:Inglês
Publié: BlackWell Publishing Ltd 2014
Sujets:
Accès en ligne: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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