Parkinson's disease prevalence in Fabry disease: A survey study

Parkinson's disease prevalence in Fabry disease: A survey study

Recent research has suggested a possible link between Parkinson's disease (PD) and Fabry disease. To test this relationship, we administered a self-report and family history questionnaire to determine the prevalence of PD in Fabry disease patients and family members with likely pathogenic alpha...

Full description

Bibliographic Details
Main Authors:	Adina H. Wise, Amy Yang, Hetanshi Naik, Chanan Stauffer, Natasha Zeid, Christopher Liong, Manisha Balwani, Robert J. Desnick, Roy N. Alcalay
Format:	Article
Language:	English
Published:	Elsevier 2018-03-01
Series:	Molecular Genetics and Metabolism Reports
Subjects:	Parkinson's disease Fabry disease Lysosomal storage disorder Alpha-galactosidase A GLA
Online Access:	http://www.sciencedirect.com/science/article/pii/S2214426917301544

Similar Items

Fabry Disease - literature review
by: Krystian Wdowiak, et al.
Published: (2024-11-01)

La malattia di Anderson-Fabry. Introduzione
by: Giovanni Duro, et al.
Published: (2017-07-01)

Genomic analysis of Brazilian patients with Fabry disease
by: F.S. Pereira, et al.
Published: (2007-12-01)

Fabry disease, a complex pathology not easy to diagnose
by: Paolo Colomba, et al.
Published: (2015-12-01)

Enfermedad de Fabry, a propósito de un caso interesante
by: Irelys González López, et al.

Might Be Fabry Disease?
by: Aysegul Oruc
Published: (2020-01-01)

THE FEATURES OE CLINICAL AND LABORATORY DIAGNOSIS OF FABRY DISEASE
by: N O. Pichkur
Published: (2017-12-01)

Genotype–Phenotype Spectrum of 52 Mexican Patients With Fabry Disease: A Novel GLA Variant With Atypical Phenotype
by: Tamara N. Kimball, et al.
Published: (2024-12-01)

The Ckd. Qld fabRy Epidemiology (aCQuiRE) study protocol: identifying the prevalence of Fabry disease amongst patients with kidney disease in Queensland, Australia
by: Andrew Mallett, et al.
Published: (2020-02-01)

Anderson-Fabry: una malattia rara?
by: Paolo Colomba, et al.
Published: (2015-06-01)

An Overview of Molecular Mechanisms in Fabry Disease
by: Federica Amodio, et al.
Published: (2022-10-01)

Fabry disease: clinical and genotypic aspects of three cases in first degree relatives
by: Leticia Bueno Nunes da Silva, et al.
Published: (2014-01-01)

Fabry disease: Mechanism and therapeutics strategies
by: Xi Li, et al.
Published: (2022-10-01)

<i>GLA</i> Mutations Suppress Autophagy and Stimulate Lysosome Generation in Fabry Disease
by: Ping Li, et al.
Published: (2024-03-01)

Multiple phenotypic domains of Fabry disease and their relevance for establishing genotype–phenotype correlations
by: Oliveira JP, et al.
Published: (2019-03-01)

AAV2/6 Gene Therapy in a Murine Model of Fabry Disease Results in Supraphysiological Enzyme Activity and Effective Substrate Reduction
by: Makiko Yasuda, et al.
Published: (2020-09-01)

Fabry disease: Four case reports of meningioma and a review of the literature on other malignancies
by: Beth L. Thurberg, MD, PhD, et al.
Published: (2017-06-01)

Doença de Fabry Fabry disease
by: Paula Boggio, et al.
Published: (2009-08-01)

What Is the Role of Sensorineural Hearing Loss in Fabry Disease Screening?
by: Ekin Yiğit Köroğlu, et al.
Published: (2023-06-01)

New mutation in Fabry disease: c.448delG, first phenotypic description
by: Esteban Calabrese, et al.
Published: (2021-06-01)

When should we think about Fabry disease?
by: Natalia Chojnacka, et al.
Published: (2024-01-01)

Anderson–Fabry Disease: A New Piece of the Lysosomal Puzzle in Parkinson Disease?
by: Marialuisa Zedde, et al.
Published: (2022-12-01)

A classical phenotype of Anderson-Fabry disease in a female patient with intronic mutations of the GLA gene: a case report
by: Pisani Antonio, et al.
Published: (2012-06-01)

Enzyme replacement therapy for Fabry disease: a systematic review and meta-analysis
by: Taciane Alegra, et al.
Published: (2012-01-01)

Cornea Verticillata in classical Fabry disease, first from Sri Lanka: a case report
by: Hasani Hewavitharana, et al.
Published: (2020-07-01)

Global research on Fabry's disease: Demands for a rare disease
by: Doris Klingelhöfer, et al.
Published: (2020-09-01)

Diagnostics of Fabry disease in arrhythmology practice: a case report
by: M. A. Dragunova, et al.
Published: (2022-08-01)

Ocular findings in Fabry disease in Colombian patients
by: Katherine Rothstein, et al.
Published: (2019-09-01)

Fabry disease screening in high-risk populations in Japan: a nationwide study
by: Shinichiro Yoshida, et al.
Published: (2020-08-01)

Reduced α-galactosidase A activity in zebrafish (Danio rerio) mirrors distinct features of Fabry nephropathy phenotype
by: Hassan O.A. Elsaid, et al.
Published: (2022-06-01)

Fabry disease exacerbates renal interstitial fibrosis after unilateral ureteral obstruction via impaired autophagy and enhanced apoptosis
by: Sungjin Chung, et al.
Published: (2021-06-01)

Characterization of small fiber pathology in a mouse model of Fabry disease
by: Lukas Hofmann, et al.
Published: (2018-10-01)

Fabry's disease manifesting as familial angiokeratoma corporis diffusum in an indian family – A rare occurrence!
by: Ishmeet Kaur, et al.
Published: (2020-01-01)

Signatures of Altered Gene Expression in Dorsal Root Ganglia of a Fabry Disease Mouse Model
by: Kai K. Kummer, et al.
Published: (2018-01-01)

The coincidence of IgA nephropathy and Fabry disease
by: Maixnerová Dita, et al.
Published: (2013-01-01)

Genotype–Phenotype Correlation in a New Fabry-Disease-Causing Mutation
by: Agnė Čerkauskaitė, et al.
Published: (2019-05-01)

High-Risk Screening for Fabry Disease: A Nationwide Study in Japan and Literature Review
by: Takaaki Sawada, et al.
Published: (2021-09-01)

Screening for Fabry Disease in Young Strokes in the Australian Stroke Clinical Registry (AuSCR)
by: Alejandra Malavera, et al.
Published: (2020-11-01)

The New Pharmacological Chaperones PBXs Increase α-Galactosidase A Activity in Fabry Disease Cellular Models
by: Pedro Besada, et al.
Published: (2021-12-01)

The Role of Cardiac MRI in the Diagnosis of Fabry Disease
by: Yoo Jin Hong, et al.
Published: (2020-03-01)