Bilimsel Makale Arama | NeuralCipher AI

Kaynak kaydı

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

Europe PMC üzerinden doğrulanabilir bibliyografik kayıt.

Makale detayına git Kaynağa git ↗

Kaynak kaydı

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

Europe PMC üzerinden doğrulanabilir bibliyografik kayıt.

Makale detayına git Kaynağa git ↗

Açık erişim

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

Europe PMC üzerinden doğrulanabilir bibliyografik kayıt.

Makale detayına git Kaynağa git ↗

Kaynak kaydı

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

Europe PMC üzerinden doğrulanabilir bibliyografik kayıt.

Makale detayına git Kaynağa git ↗

Kaynak kaydı

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

Europe PMC üzerinden doğrulanabilir bibliyografik kayıt.

Makale detayına git Kaynağa git ↗

Kaynak kaydı

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

Europe PMC üzerinden doğrulanabilir bibliyografik kayıt.

Makale detayına git Kaynağa git ↗

Kaynak kaydı

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

Europe PMC üzerinden doğrulanabilir bibliyografik kayıt.

Makale detayına git Kaynağa git ↗

Açık erişim

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

Europe PMC üzerinden doğrulanabilir bibliyografik kayıt.

Makale detayına git Kaynağa git ↗

Kaynak kaydı

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

Europe PMC üzerinden doğrulanabilir bibliyografik kayıt.

Makale detayına git Kaynağa git ↗

Kaynak kaydı

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

Europe PMC üzerinden doğrulanabilir bibliyografik kayıt.

Makale detayına git Kaynağa git ↗

Kaynak kaydı

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

Europe PMC üzerinden doğrulanabilir bibliyografik kayıt.

Makale detayına git Kaynağa git ↗

Kaynak kaydı

GBA mutations and Parkinson disease: when genotype meets phenotype.

Scholz SW, Jeon BS.

Neurology · 2015-02-04

DOI: 10.1212/wnl.0000000000001321PMID: 25653294

Europe PMC üzerinden doğrulanabilir bibliyografik kayıt.

Makale detayına git Kaynağa git ↗

Kayıtlar bilimsel kaynaklardan alınır. Bibliyografik kayıt sayısı, Türkçe çeviri veya editoryal onay sayısı değildir.

404 makale bulundu

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.

Filtreler