GBA mutations, glucosylceramide and Parkinson's disease-Reference-Cited by-同舟云学术

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GBA mutations, glucosylceramide and Parkinson's disease

Published:2022-02 Issue: Volume:72 Page:148-154
ISSN:0959-4388
Container-title:Current Opinion in Neurobiology
language:en
Short-container-title:Current Opinion in Neurobiology

Author:

Milenkovic Ivan^ORCID,Blumenreich Shani,Futerman Anthony H.

Publisher

Elsevier BV

Subject

General Neuroscience

Reference42 articles.

1. MDS clinical diagnostic criteria for Parkinson's disease;Postuma;Mov Disord,2015

2. Alpha-synuclein in Lewy bodies;Spillantini;Nature,1997

3. Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease;Robak;Brain,2017

4. Lysosomal storage disorders shed light on lysosomal dysfunction in Parkinson's disease;Blumenreich;Int J Mol Sci,2020

5. Recent advances;Schapira;Mol Cell Neurosci,2015

Cited by 30 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. Gaucher disease provides a unique window into Parkinson disease pathogenesis;Nature Reviews Neurology;2024-08-06

2. A review of sphingolipids from marine sources and their analytical method, metabolic process, and essential roles in human health;Food Frontiers;2024-07-28

3. Evaluation of a Liquid Chromatography–Tandem Mass Spectrometry Method for the Analysis of Glucosylceramide and Galactosylceramide Isoforms in Cerebrospinal Fluid of Parkinson’s Disease Patients;Analytical Chemistry;2024-07-24

4. Neurological symptoms in adults with Gaucher disease: a systematic review;Journal of Neurology;2024-05-21

5. Targeting lysosomal quality control as a therapeutic strategy against aging and diseases;Medicinal Research Reviews;2024-05-06

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