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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Xehetasun bibliografikoak
Argitaratua izan da:Ann Clin Transl Neurol
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BlackWell Publishing Ltd 2014
Gaiak:
Research Articles
Sarrera elektronikoa: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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