Parkinsonism in Patients with Neuronopathic (Type 3) Gaucher Disease: A Case Series-Reference-Cited by-同舟云学术

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Parkinsonism in Patients with Neuronopathic (Type 3) Gaucher Disease: A Case Series

Published:2020-08-17 Issue:7 Volume:7 Page:834-837
ISSN:2330-1619
Container-title:Movement Disorders Clinical Practice
language:en
Short-container-title:Mov Disord Clin Pract

Author:

Ryan Emory¹,Amato Dominick²,MacKenzie Jennifer J.³⁴,Sidransky Ellen¹,Lopez Grisel¹

Affiliation:

1. National Human Genome Research Institute, National Institutes of Health Bethesda Maryland USA

2. Mark Freedman and Judy Jacobs Program for Gaucher Disease, Mount Sinai Hospital Toronto Ontario Canada

3. McMaster University Hamilton Ontario Canada

4. Queen's University Kingston Ontario Canada

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mdc3.13031

Reference10 articles.

1. Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

2. The definition of neuronopathic Gaucher disease [published online ahead of print April 3, 2020];Schiffmann R;J Inherit Metab Dis

3. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases.

4. Prodromal PD: A new nosological entity

5. Gaucher Disease and Parkinsonism: A Phenotypic and Genotypic Characterization

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Acid ceramidase involved in pathogenic cascade leading to accumulation of α-synuclein in iPSC model of GBA1-associated Parkinson’s disease;Human Molecular Genetics;2023-02-08

2. The diagnosis and management of Gaucher disease in pediatric patients: Where do we go from here?;Molecular Genetics and Metabolism;2022-05

3. Parkinsonism and ataxia;Journal of the Neurological Sciences;2022-02

4. Gaucher disease – more than just a rare lipid storage disease;Journal of Molecular Medicine;2022-01-23

5. Diagnosing neuronopathic Gaucher disease: New considerations and challenges in assigning Gaucher phenotypes;Molecular Genetics and Metabolism;2021-02

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