HuGE Literature Finder
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PREDICT-PD: An online approach to prospectively identify risk indicators of Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2017 Jan . Noyce Alastair J, R'Bibo Lea, Peress Luisa, Bestwick Jonathan P, Adams-Carr Kerala L, Mencacci Niccolo E, Hawkes Christopher H, Masters Joseph M, Wood Nicholas, Hardy John, Giovannoni Gavin, Lees Andrew J, Schrag Anet |
Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene. Movement disorders : official journal of the Movement Disorder Society 2015 Jun 30 (7): 981-6. Mirelman Anat, Alcalay Roy N, Saunders-Pullman Rachel, Yasinovsky Kira, Thaler Avner, Gurevich Tanya, Mejia-Santana Helen, Raymond Deborah, Gana-Weisz Mali, Bar-Shira Anat, Ozelius Laurie, Clark Lorraine, Orr-Urtreger Avi, Bressman Susan, Marder Karen, Giladi Nir, |
Olfactory dysfunction in sporadic Parkinson's Disease and LRRK2 carriers. Acta neurologica Scandinavica 2014 May 129 (5): 300-6. Johansen K K, Warø B J, Aasly J |
Nonmotor symptoms in LRRK2 G2019S associated Parkinson's disease. PloS one 2014 9 (10): e108982. Gaig Carles, Vilas Dolores, Infante Jon, Sierra María, García-Gorostiaga Inés, Buongiorno Mariateresa, Ezquerra Mario, Martí Maria José, Valldeoriola Francesc, Aguilar Miquel, Calopa Matilde, Hernandez-Vara Jorge, Tolosa Eduar |
Cognitive performance of GBA mutation carriers with early-onset PD: the CORE-PD study. Neurology 2012 May 78 (18): 1434-40. Alcalay R N, Caccappolo E, Mejia-Santana H, Tang M -X, Rosado L, Orbe Reilly M, Ruiz D, Ross B, Verbitsky M, Kisselev S, Louis E, Comella C, Colcher A, Jennings D, Nance M, Bressman S, Scott W K, Tanner C, Mickel S, Andrews H, Waters C, Fahn S, Cote L, Frucht S, Ford B, Rezak M, Novak K, Friedman J H, Pfeiffer R, Marsh L, Hiner B, Siderowf A, Payami H, Molho E, Factor S, Ottman R, Clark L N, Marder |
Olfactory deficits and cardiac 123I-MIBG in Parkinson's disease related to the LRRK2 R1441G and G2019S mutations. Movement disorders : official journal of the Movement Disorder Society 2011 Sep 26 (11): 2026-31. Ruiz-Martínez Javier, Gorostidi Ana, Goyenechea Estibaliz, Alzualde Ainhoa, Poza Juan José, Rodríguez Francisco, Bergareche Alberto, Moreno Fermín, López de Munain Adolfo, Martí Massó José |
Olfactory dysfunction in LRRK2 G2019S mutation carriers. Neurology 2011 Jul 77 (4): 319-24. Saunders-Pullman R, Stanley K, Wang C, San Luciano M, Shanker V, Hunt A, Severt L, Raymond D, Ozelius L J, Lipton R B, Bressman S |
Olfactory heterogeneity in LRRK2 related Parkinsonism. Movement disorders : official journal of the Movement Disorder Society 2010 Dec 25 (16): 2879-83. Silveira-Moriyama Laura, Munhoz Renato Pupi, de J Carvalho Margarete, Raskin Salmo, Rogaeva Ekaterina, de C Aguiar Patricia, Bressan Rodrigo A, Felicio Andre C, Barsottini Orlando G P, Andrade Luiz Augusto F, Chien Hsin F, Bonifati Vincenzo, Barbosa Egberto R, Teive Helio A, Lees Andrew |
Hyposmia in G2019S LRRK2-related parkinsonism: clinical and pathologic data. Neurology 2008 Sep 71 (13): 1021-6. Silveira-Moriyama L, Guedes L C, Kingsbury A, Ayling H, Shaw K, Barbosa E R, Bonifati V, Quinn N P, Abou-Sleiman P, Wood N W, Petrie A, Sampaio C, Ferreira J J, Holton J, Revesz T, Lees A |
High prevalence of LRRK2 mutations in familial and sporadic Parkinson's disease in Portugal. Movement disorders : official journal of the Movement Disorder Society 2007 Jun 22 (8): 1194-201. Ferreira Joaquim J, Guedes Leonor Correia, Rosa Mário Miguel, Coelho Miguel, van Doeselaar Marina, Schweiger Dorothea, Di Fonzo Alessio, Oostra Ben A, Sampaio Cristina, Bonifati Vincen |
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