Parkinson Disease Phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutations

BACKGROUND: The phenotype of Parkinson disease (PD) patients with and without LRRK2 G2019S mutations is reported to be similar; however large uniformly evaluated series are lacking. OBJECTIVE: To characterize the clinical phenotype of Ashkenazi Jewish (AJ) PD carriers of the LRRK2 G2019S mutation. M...

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Main Authors: Alcalay, Roy N., Mirelman, Anat, Saunders-Pullman, Rachel, Tang, Ming-X, Santana, Helen Mejia, Raymond, Deborah, Roos, Ernest, Orbe-Reilly, Martha, Gurevich, Tanya, Shira, Anat Bar, Weisz, Mali Gana, Yasinovsky, Kira, Zalis, Maayan, Thaler, Avner, Deik, Andres, Barrett, Matthew James, Cabassa, Jose, Groves, Mark, Hunt, Ann L., Lubarr, Naomi, Luciano, Marta San, Miravite, Joan, Palmese, Christina, Sachdev, Rivka, Sarva, Harini, Severt, Lawrence, Shanker, Vicki, Swan, Matthew Carrington, Soto-Valencia, Jeannie, Johannes, Brooke, Ortega, Robert, Fahn, Stanley, Cote, Lucien, Waters, Cheryl, Mazzoni, Pietro, Ford, Blair, Louis, Elan, Levy, Oren, Rosado, Llency, Ruiz, Diana, Dorovski, Tsvyatko, Pauciulo, Michael, Nichols, William, Orr-Urtreger, Avi, Ozelius, Laurie, Clark, Lorraine, Giladi, Nir, Bressman, Susan, Marder, Karen S
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3859844/
https://ncbi.nlm.nih.gov/pubmed/24243757
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.25647
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