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Differential effects of severe vs mild GBA mutations on Parkinson disease.

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

Neurology · 2015-02-04

DOI: 10.1212/wnl.0000000000001315PMID: 25653295

A bibliographic record traceable to Europe PMC.

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Evolution of prodromal clinical markers of Parkinson disease in a GBA mutation-positive cohort.

Beavan M, McNeill A, Proukakis C, Hughes DA, Mehta A, Schapira AH.

JAMA Neurol · 2015-02-01

DOI: 10.1001/jamaneurol.2014.2950PMID: 25506732

A bibliographic record traceable to Europe PMC.

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GBA-associated Parkinson's disease: reduced survival and more rapid progression in a prospective longitudinal study.

Brockmann K, Srulijes K, Pflederer S, Hauser AK, Schulte C, Maetzler W, Gasser T, Berg D.

Mov Disord · 2014-12-01

DOI: 10.1002/mds.26071PMID: 25448271

A bibliographic record traceable to Europe PMC.

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Open access

Visual short-term memory deficits associated with GBA mutation and Parkinson's disease.

Zokaei N, McNeill A, Proukakis C, Beavan M, Jarman P, Korlipara P, Hughes D, Mehta A, Hu MT, Schapira AH, Husain M.

Brain · 2014-06-11

DOI: 10.1093/brain/awu143PMID: 24919969

A bibliographic record traceable to Europe PMC.

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iPSC-derived neurons from GBA1-associated Parkinson's disease patients show autophagic defects and impaired calcium homeostasis.

Schöndorf DC, Aureli M, McAllister FE, Hindley CJ, Mayer F, Schmid B, Sardi SP, Valsecchi M, Hoffmann S, Schwarz LK, Hedrich U, Berg D, Shihabuddin LS, Hu J, Pruszak J, Gygi SP, Sonnino S, Gasser T, Deleidi M.

Nat Commun · 2014-06-06

DOI: 10.1038/ncomms5028PMID: 24905578

A bibliographic record traceable to Europe PMC.

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The significance of GBA for Parkinson's disease.

Brockmann K, Berg D.

J Inherit Metab Dis · 2014-06-04

DOI: 10.1007/s10545-014-9714-7PMID: 24894157

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Comparison of Parkinson risk in Ashkenazi Jewish patients with Gaucher disease and GBA heterozygotes.

Alcalay RN, Dinur T, Quinn T, Sakanaka K, Levy O, Waters C, Fahn S, Dorovski T, Chung WK, Pauciulo M, Nichols W, Rana HQ, Balwani M, Bier L, Elstein D, Zimran A.

JAMA Neurol · 2014-06-01

DOI: 10.1001/jamaneurol.2014.313PMID: 24756352

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Clinicogenetic study of GBA mutations in patients with familial Parkinson's disease.

Li Y, Sekine T, Funayama M, Li L, Yoshino H, Nishioka K, Tomiyama H, Hattori N.

Neurobiol Aging · 2013-10-12

DOI: 10.1016/j.neurobiolaging.2013.09.019PMID: 24126159

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

404 articles found

Differential effects of severe vs mild GBA mutations on Parkinson disease.

Evolution of prodromal clinical markers of Parkinson disease in a GBA mutation-positive cohort.

GBA-associated Parkinson's disease: reduced survival and more rapid progression in a prospective longitudinal study.

Visual short-term memory deficits associated with GBA mutation and Parkinson's disease.

iPSC-derived neurons from GBA1-associated Parkinson's disease patients show autophagic defects and impaired calcium homeostasis.

The significance of GBA for Parkinson's disease.

Comparison of Parkinson risk in Ashkenazi Jewish patients with Gaucher disease and GBA heterozygotes.

Clinicogenetic study of GBA mutations in patients with familial Parkinson's disease.

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