Increased glucosylsphingosine levels and Gaucher disease in GBA1-associated Parkinson's disease

Author:

Marano MassimoORCID,Zizzo Carmela,Malaguti Maria ChiaraORCID,Bacchin RuggeroORCID,Cavallieri Francesco,De Micco RosaORCID,Spagnolo Francesca,Bentivoglio Anna Rita,Schirinzi Tommaso,Bovenzi Roberta,Ramat Silvia,Erro Roberto,Sorrentino CristianoORCID,Sucapane Patrizia,Pilotto Andrea,Lupini AlessandroORCID,Magliozzi Alessandro,Di Vico IlariaORCID,Carecchio MiryamORCID,Bonato Giulia,Cilia Roberto,Colucci Fabiana,Tamma FilippoORCID,Caputo Elena,Mostile Giovanni,Arabia Gennarina,Modugno Nicola,Zibetti Maurizio,Ceravolo Maria Gabriella,Tambasco Nicola,Cossu Giovanni,Valzania Franco,Manganotti Paolo,Di Lazzaro VincenzoORCID,Zappia Mario,Fabbrini Giovanni,Tinazzi Michele,Tessitore Alessandro,Duro Giovanni,Di Fonzo AlessioORCID

Publisher

Elsevier BV

Reference35 articles.

1. Lysosomal functions and dysfunctions: molecular and cellular mechanisms underlying Gaucher disease and its association with Parkinson disease;Horowitz;Adv. Drug Deliv. Rev.,2022

2. Contribution of glucosylsphingosine (Lyso-Gb1) to Treatment Decisions in patients with Gaucher disease;Dinur;Int. J. Mol. Sci.,2023

3. Gaucher disease types 1 and 3: phenotypic characterization of large populations from the ICGG Gaucher Registry;Grabowski;Am. J. Hematol.,2015

4. GBA1 p.T369M substitution in Parkinson disease: polymorphism or association? A meta-analysis;Mallett;Neurol Genet,2016

5. The E326K mutation and Gaucher disease: mutation or polymorphism?;Park;Clin. Genet.,2002

Cited by 1 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. GBA1-Associated Parkinson’s Disease Is a Distinct Entity;International Journal of Molecular Sciences;2024-06-28

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