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GBA-Associated Parkinson's Disease: Progression in a Deep Brain Stimulation Cohort.

Lythe V, Athauda D, Foley J, Mencacci NE, Jahanshahi M, Cipolotti L, Hyam J, Zrinzo L, Hariz M, Hardy J, Limousin P, Foltynie T.

J Parkinsons Dis · 2017-01-01

DOI: 10.3233/jpd-171172PMID: 28777757

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[The clinical features of Parkinson's disease in patients with mutations and polymorphic variants of GBA gene].

Senkevich KA, Miliukhina IV, Beletskaia MV, Gracheva EV, Kudrevatykh AV, Nikolaev MA, Emelyanov AK, Kopytova AE, Timofeeva AA, Yakimovskii AF, Pchelina SN.

Zh Nevrol Psikhiatr Im S S Korsakova · 2017-01-01

DOI: 10.17116/jnevro201711710181-86PMID: 29171494

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Open access

GBA Variants Influence Motor and Non-Motor Features of Parkinson's Disease.

Jesús S, Huertas I, Bernal-Bernal I, Bonilla-Toribio M, Cáceres-Redondo MT, Vargas-González L, Gómez-Llamas M, Carrillo F, Calderón E, Carballo M, Gómez-Garre P, Mir P.

PLoS One · 2016-12-28

DOI: 10.1371/journal.pone.0167749PMID: 28030538

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Open access

Commentary: Parkinson disease-linked GBA mutation effects reversed by molecular chaperones in human cell and fly models.

Fernandes HJ, Ryan BJ, Wade-Martins R.

Front Neurosci · 2016-12-23

DOI: 10.3389/fnins.2016.00578PMID: 28066164

A bibliographic record traceable to Europe PMC.

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A "dose" effect of mutations in the GBA gene on Parkinson's disease phenotype.

Thaler A, Gurevich T, Bar Shira A, Gana Weisz M, Ash E, Shiner T, Orr-Urtreger A, Giladi N, Mirelman A.

Parkinsonism Relat Disord · 2016-12-16

DOI: 10.1016/j.parkreldis.2016.12.014PMID: 28012950

A bibliographic record traceable to Europe PMC.

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Oligomeric α-synuclein and glucocerebrosidase activity levels in GBA-associated Parkinson's disease.

Pchelina S, Emelyanov A, Baydakova G, Andoskin P, Senkevich K, Nikolaev M, Miliukhina I, Yakimovskii A, Timofeeva A, Fedotova E, Abramycheva N, Usenko T, Kulabukhova D, Lavrinova A, Kopytova A, Garaeva L, Nuzhnyi E, Illarioshkin S, Zakharova E.

Neurosci Lett · 2016-10-22

DOI: 10.1016/j.neulet.2016.10.039PMID: 27780739

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Autosomal dominant Parkinson's disease: Incidence of mutations in LRRK2, SNCA, VPS35 and GBA genes in Brazil.

Abreu GM, Valença DC, Campos M, da Silva CP, Pereira JS, Araujo Leite MA, Rosso AL, Nicaretta DH, Vasconcellos LF, da Silva DJ, Della Coletta MV, Dos Santos JM, Gonçalves AP, Santos-Rebouças CB, Pimentel MM.

Neurosci Lett · 2016-10-21

DOI: 10.1016/j.neulet.2016.10.040PMID: 27777137

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Survival and dementia in GBA-associated Parkinson's disease: The mutation matters.

Cilia R, Tunesi S, Marotta G, Cereda E, Siri C, Tesei S, Zecchinelli AL, Canesi M, Mariani CB, Meucci N, Sacilotto G, Zini M, Barichella M, Magnani C, Duga S, Asselta R, Soldà G, Seresini A, Seia M, Pezzoli G, Goldwurm S.

Ann Neurol · 2016-10-03

DOI: 10.1002/ana.24777PMID: 27632223

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Association of GBA Mutations and the E326K Polymorphism With Motor and Cognitive Progression in Parkinson Disease.

Davis MY, Johnson CO, Leverenz JB, Weintraub D, Trojanowski JQ, Chen-Plotkin A, Van Deerlin VM, Quinn JF, Chung KA, Peterson-Hiller AL, Rosenthal LS, Dawson TM, Albert MS, Goldman JG, Stebbins GT, Bernard B, Wszolek ZK, Ross OA, Dickson DW, Eidelberg D, Mattis PJ, Niethammer M, Yearout D, Hu SC, Cholerton BA, Smith M, Mata IF, Montine TJ, Edwards KL, Zabetian CP.

JAMA Neurol · 2016-10-01

DOI: 10.1001/jamaneurol.2016.2245PMID: 27571329

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Open access

GBA p.T369M substitution in Parkinson disease: Polymorphism or association? A meta-analysis.

Mallett V, Ross JP, Alcalay RN, Ambalavanan A, Sidransky E, Dion PA, Rouleau GA, Gan-Or Z.

Neurol Genet · 2016-09-08

DOI: 10.1212/nxg.0000000000000104PMID: 27648471

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Neuropsychiatric characteristics of GBA-associated Parkinson disease.

Swan M, Doan N, Ortega RA, Barrett M, Nichols W, Ozelius L, Soto-Valencia J, Boschung S, Deik A, Sarva H, Cabassa J, Johannes B, Raymond D, Marder K, Giladi N, Miravite J, Severt W, Sachdev R, Shanker V, Bressman S, Saunders-Pullman R.

J Neurol Sci · 2016-08-30

DOI: 10.1016/j.jns.2016.08.059PMID: 27772789

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Open access

Parkinson disease-linked GBA mutation effects reversed by molecular chaperones in human cell and fly models.

Sanchez-Martinez A, Beavan M, Gegg ME, Chau KY, Whitworth AJ, Schapira AH.

Sci Rep · 2016-08-19

DOI: 10.1038/srep31380PMID: 27539639

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Records come from scientific sources. Bibliographic counts do not represent completed translations or editorial approvals.

404 articles found

GBA-Associated Parkinson's Disease: Progression in a Deep Brain Stimulation Cohort.

[The clinical features of Parkinson's disease in patients with mutations and polymorphic variants of GBA gene].

GBA Variants Influence Motor and Non-Motor Features of Parkinson's Disease.

Commentary: Parkinson disease-linked GBA mutation effects reversed by molecular chaperones in human cell and fly models.

A "dose" effect of mutations in the GBA gene on Parkinson's disease phenotype.

Oligomeric α-synuclein and glucocerebrosidase activity levels in GBA-associated Parkinson's disease.

Autosomal dominant Parkinson's disease: Incidence of mutations in LRRK2, SNCA, VPS35 and GBA genes in Brazil.

Survival and dementia in GBA-associated Parkinson's disease: The mutation matters.

Association of GBA Mutations and the E326K Polymorphism With Motor and Cognitive Progression in Parkinson Disease.

GBA p.T369M substitution in Parkinson disease: Polymorphism or association? A meta-analysis.

Neuropsychiatric characteristics of GBA-associated Parkinson disease.

Parkinson disease-linked GBA mutation effects reversed by molecular chaperones in human cell and fly models.

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