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Comment
. 2022 Aug;37(8):1779-1781.
doi: 10.1002/mds.29132. Epub 2022 Jul 6.

Could Blood Hexosylsphingosine Be a Marker for Parkinson's Disease Linked with GBA1 Mutations?

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Comment

Could Blood Hexosylsphingosine Be a Marker for Parkinson's Disease Linked with GBA1 Mutations?

Alena E Kopytova et al. Mov Disord. 2022 Aug.
No abstract available

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References

    1. Surface M, Balwani M, Waters C, et al. Plasma glucosylsphingosine in GBA1 mutation carriers with and without Parkinson's disease. Mov Disord 2022;37(2):416-421. https://doi.org/10.1002/mds.28846
    1. Gleason A, Tayebi N, Lopez G, Sidransky E. No evidence that glucosylsphingosine is a biomarker for Parkinson's disease: statistical differences do not necessarily indicate biological significance. Mov Disord 2022;37(3):653. https://doi.org/10.1002/mds.28935
    1. Pchelina S, Emelyanov A, Baydakova G, et al. Oligomeric alpha-synuclein and glucocerebrosidase activity levels in GBA-associated Parkinson's disease. Neurosci Lett 2017;636:70-76. https://doi.org/10.1016/j.neulet.2016.10.039
    1. Pchelina S, Baydakova G, Nikolaev M, et al. Blood lysosphingolipids accumulation in patients with parkinson's disease with glucocerebrosidase 1 mutations. Mov Disord 2018;33(8):1316-1321. https://doi.org/10.1002/mds.27393
    1. Polo G, Burlina AP, Ranieri E, et al. Plasma and dried blood spot lysosphingolipids for the diagnosis of different sphingolipidoses: a comparative study. Clin Chem Lab Med 2019;57(12):1863-1874. https://doi.org/10.1515/cclm-2018-1301

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