Parkinson Disease Phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutations
Identifieur interne : 000371 ( Pmc/Corpus ); précédent : 000370; suivant : 000372Parkinson Disease Phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutations
Auteurs : Roy N. Alcalay ; Anat Mirelman ; Rachel Saunders-Pullman ; Ming-X Tang ; Helen Mejia Santana ; Deborah Raymond ; Ernest Roos ; Martha Orbe-Reilly ; Tanya Gurevich ; Anat Bar Shira ; Mali Gana Weisz ; Kira Yasinovsky ; Maayan Zalis ; Avner Thaler ; Andres Deik ; Matthew James Barrett ; Jose Cabassa ; Mark Groves ; Ann L. Hunt ; Naomi Lubarr ; Marta San Luciano ; Joan Miravite ; Christina Palmese ; Rivka Sachdev ; Harini Sarva ; Lawrence Severt ; Vicki Shanker ; Matthew Carrington Swan ; Jeannie Soto-Valencia ; Brooke Johannes ; Robert Ortega ; Stanley Fahn ; Lucien Cote ; Cheryl Waters ; Pietro Mazzoni ; Blair Ford ; Elan Louis ; Oren Levy ; Llency Rosado ; Diana Ruiz ; Tsvyatko Dorovski ; Michael Pauciulo ; William Nichols ; Avi Orr-Urtreger ; Laurie Ozelius ; Lorraine Clark ; Nir Giladi ; Susan Bressman ; Karen S. MarderSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2013.
Abstract
The phenotype of Parkinson disease (PD) patients with and without
To characterize the clinical phenotype of Ashkenazi Jewish (AJ) PD carriers of the
We studied 553 AJ PD patients, including 65 patients who were previously reported, from three sites (two in New York and one in Tel-Aviv).
PD in AJ-
Url:
DOI: 10.1002/mds.25647
PubMed: 24243757
PubMed Central: 3859844
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