GBA mutations in Parkinson disease: earlier death but similar neuropathological features-Reference-Cited by-同舟云学术

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GBA mutations in Parkinson disease: earlier death but similar neuropathological features

Published:2017-08-17 Issue:11 Volume:24 Page:1363-1368
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Eur J Neurol

Author:

Adler C. H.¹^ORCID,Beach T. G.²,Shill H. A.³,Caviness J. N.¹,Driver-Dunckley E.¹,Sabbagh M. N.³,Patel A.¹,Sue L. I.²,Serrano G.²,Jacobson S. A.⁴,Davis K.⁴,Belden C. M.⁴,Dugger B. N.²⁵,Paciga S. A.⁶^ORCID,Winslow A. R.⁶,Hirst W. D.⁶,Hentz J. G.⁷

Affiliation:

1. Department of Neurology; Parkinson's Disease and Movement Disorders Center; Mayo Clinic Arizona; Scottsdale AZ USA

2. Civin Laboratory for Neuropathology; Banner Sun Health Research Institute; Sun City AZ USA

3. Barrow Neurological Institute; Phoenix AZ USA

4. Cleo Roberts Center; Banner Sun Health Research Institute; Sun City AZ USA

5. University of California; San Francisco CA USA

6. Pfizer Neuroscience Research Unit; Cambridge MA USA

7. Department of Biostatistics; Mayo Clinic Arizona; Scottsdale AZ USA

Funder

National Institute of Neurological Disorders and Stroke

National Institute on Aging

Arizona Biomedical Research Commission

Michael J. Fox Foundation for Parkinson's Research

Mayo Clinic

National Institutes of Health

Arizona Biomedical Research Foundation

Axovant

Cynapsus/Sunovion

Avid Radiopharmaceuticals/Eli Lilly Corporation

Bayer HealthCare

GE Healthcare

Navidea Healthcare

Quintiles

Genentech

Pfizer

Avid

Elan

Eli Lilly and Company

Avanir

DART Neurosciences

Neuronix

Navidea

Functional Neuromodulation

Roche

Novartis

AbbVie

Janssen Pharmaceuticals

Intracellular

Biotie

Biogen

Astra Zeneca

Merck

TransTech Pharma

Takeda/Zinfindel

International Essential Tremor Foundation

CurePSP Foundation

Henry M. Jackson Foundation

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ene.13395/fullpdf

Reference29 articles.

1. Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset;Sidransky;Neurology,2009

2. Glucocerebrosidase mutations in primary parkinsonism;Asselta;Park Relat Disord,2014

3. Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease;Neumann;Brain,2009

4. Lysosomal hydrolases in cerebrospinal fluid from subjects with Parkinson's disease;Balducci;Mov Disord,2007

5. Reduced glucocerebrosidase is associated with increased alpha-synuclein in sporadic Parkinson's disease;Murphy;Brain,2014

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1. Role of GBA variants in Lewy body disease neuropathology;Acta Neuropathologica;2024-03-12

2. A severe neurodegenerative disease with Lewy bodies and a mutation in the glucocerebrosidase gene;npj Parkinson's Disease;2023-04-05

3. SWATH Mass Spectrometry-Based CSF Proteome Profile of GBA-Linked Parkinson’s Disease Patients;International Journal of Molecular Sciences;2022-11-16

4. Skin alpha-synuclein deposit patterns: A predictor of Parkinson's disease subtypes;eBioMedicine;2022-06

5. Neuropathological Features of Gaucher Disease and Gaucher Disease with Parkinsonism;International Journal of Molecular Sciences;2022-05-23

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