Scientific Literature Search

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The Neuropsychiatric and Motor Profile of <i>GBA</i>-Associated Parkinson's Disease: A Review.

Pal G, Robertson E, O'Keefe J, Hall D.

Mov Disord Clin Pract · 2015-09-16

DOI: 10.1002/mdc3.12229PMID: 30363594

A bibliographic record traceable to Europe PMC.

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Down-regulation of B cell-related genes in peripheral blood leukocytes of Parkinson's disease patients with and without GBA mutations.

Kobo H, Bar-Shira A, Dahary D, Gan-Or Z, Mirelman A, Goldstein O, Giladi N, Orr-Urtreger A.

Mol Genet Metab · 2015-09-14

DOI: 10.1016/j.ymgme.2015.09.005PMID: 26410072

A bibliographic record traceable to Europe PMC.

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Open access

Effect of GBA Mutations on Phenotype of Parkinson's Disease: A Study on Chinese Population and a Meta-Analysis.

Zhang Y, Sun QY, Zhao YW, Shu L, Guo JF, Xu Q, Yan XX, Tang BS.

Parkinsons Dis · 2015-09-02

DOI: 10.1155/2015/916971PMID: 26421210

A bibliographic record traceable to Europe PMC.

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GBA Variants are associated with a distinct pattern of cognitive deficits in Parkinson's disease.

Mata IF, Leverenz JB, Weintraub D, Trojanowski JQ, Chen-Plotkin A, Van Deerlin VM, Ritz B, Rausch R, Factor SA, Wood-Siverio C, Quinn JF, Chung KA, Peterson-Hiller AL, Goldman JG, Stebbins GT, Bernard B, Espay AJ, Revilla FJ, Devoto J, Rosenthal LS, Dawson TM, Albert MS, Tsuang D, Huston H, Yearout D, Hu SC, Cholerton BA, Montine TJ, Edwards KL, Zabetian CP.

Mov Disord · 2015-08-21

DOI: 10.1002/mds.26359PMID: 26296077

A bibliographic record traceable to Europe PMC.

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The Alzheimer disease BIN1 locus as a modifier of GBA-associated Parkinson disease.

Gan-Or Z, Amshalom I, Bar-Shira A, Gana-Weisz M, Mirelman A, Marder K, Bressman S, Giladi N, Orr-Urtreger A.

J Neurol · 2015-08-02

DOI: 10.1007/s00415-015-7868-3PMID: 26233692

A bibliographic record traceable to Europe PMC.

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Glucocerebrosidase activity in Parkinson's disease with and without GBA mutations.

Alcalay RN, Levy OA, Waters CC, Fahn S, Ford B, Kuo SH, Mazzoni P, Pauciulo MW, Nichols WC, Gan-Or Z, Rouleau GA, Chung WK, Wolf P, Oliva P, Keutzer J, Marder K, Zhang X.

Brain · 2015-06-27

DOI: 10.1093/brain/awv179PMID: 26117366

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Ambroxol-induced rescue of defective glucocerebrosidase is associated with increased LIMP-2 and saposin C levels in GBA1 mutant Parkinson's disease cells.

Ambrosi G, Ghezzi C, Zangaglia R, Levandis G, Pacchetti C, Blandini F.

Neurobiol Dis · 2015-06-19

DOI: 10.1016/j.nbd.2015.06.008PMID: 26094596

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Open access

No evidence for substrate accumulation in Parkinson brains with GBA mutations.

Gegg ME, Sweet L, Wang BH, Shihabuddin LS, Sardi SP, Schapira AH.

Mov Disord · 2015-06-11

DOI: 10.1002/mds.26278PMID: 26096906

A bibliographic record traceable to Europe PMC.

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Web-based assessment of Parkinson's prodromal markers identifies GBA variants.

Noyce AJ, Mencacci NE, Schrag A, Bestwick JP, Giovannoni G, Lees AJ, Hardy J.

Mov Disord · 2015-05-13

DOI: 10.1002/mds.26249PMID: 25970725

A bibliographic record traceable to Europe PMC.

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Association of LRRK2 and GBA mutations in a Brazilian family with Parkinson's disease.

Spitz M, Pereira JS, Nicareta DH, Abreu Gde M, Bastos EF, Seixas TL, Pimentel MM.

Parkinsonism Relat Disord · 2015-05-02

DOI: 10.1016/j.parkreldis.2015.03.029PMID: 25952961

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Presenting symptoms of GBA-related Parkinson's disease.

Kresojević N, Janković M, Petrović I, Kumar KR, Dragašević N, Dobričić V, Novaković I, Svetel M, Klein C, Pekmezović T, Kostić VS.

Parkinsonism Relat Disord · 2015-05-01

DOI: 10.1016/j.parkreldis.2015.04.028PMID: 25957717

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GBA mutations and Parkinson disease: when genotype meets phenotype.

Scholz SW, Jeon BS.

Neurology · 2015-02-04

DOI: 10.1212/wnl.0000000000001321PMID: 25653294

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

404 articles found

The Neuropsychiatric and Motor Profile of <i>GBA</i>-Associated Parkinson's Disease: A Review.

Down-regulation of B cell-related genes in peripheral blood leukocytes of Parkinson's disease patients with and without GBA mutations.

Effect of GBA Mutations on Phenotype of Parkinson's Disease: A Study on Chinese Population and a Meta-Analysis.

GBA Variants are associated with a distinct pattern of cognitive deficits in Parkinson's disease.

The Alzheimer disease BIN1 locus as a modifier of GBA-associated Parkinson disease.

Glucocerebrosidase activity in Parkinson's disease with and without GBA mutations.

Ambroxol-induced rescue of defective glucocerebrosidase is associated with increased LIMP-2 and saposin C levels in GBA1 mutant Parkinson's disease cells.

No evidence for substrate accumulation in Parkinson brains with GBA mutations.

Web-based assessment of Parkinson's prodromal markers identifies GBA variants.

Association of LRRK2 and GBA mutations in a Brazilian family with Parkinson's disease.

Presenting symptoms of GBA-related Parkinson's disease.

GBA mutations and Parkinson disease: when genotype meets phenotype.

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