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Comment
. 2023 May 30;100(22):1075.
doi: 10.1212/WNL.0000000000207416.

Author Response: D313Y Variant in Fabry Disease: A Systematic Review and Meta-analysis

Lina Palaiodimou  1 , Maria-Ioanna Stefanou  1 , Georgios Tsivgoulis  1
Affiliations
Comment

Author Response: D313Y Variant in Fabry Disease: A Systematic Review and Meta-analysis

Lina Palaiodimou et al. Neurology. .
No abstract available

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References

    1. Palaiodimou L, Stefanou MI, Bakola E, et al. . D313Y variant in Fabry disease: a systematic review and meta-analysis. Neurology. 2022;99(19):e2188-e2200. - PubMed
    1. Lackova A, Beetz C, Oppermann S, et al. . Prevalence of Fabry disease among patients with Parkinson's disease. Parkinson's Dis. 2022;2022:1014950. - PMC - PubMed
    1. Palaiodimou L, Kokotis P, Zompola C, et al. . Fabry disease: current and novel therapeutic strategies. A narrative review. Curr Neuropharmacol. 2023;21(3):440-456. - PMC - PubMed
    1. Colomba P, Zizzo C, Alessandro R, et al. . Fabry disease and multiple sclerosis misdiagnosis: the role of family history and neurological signs. Oncotarget. 2018;9(8):7758-7762. - PMC - PubMed
    1. Zompola C, Palaiodimou L, Kokotis P, et al. . The mutation D313Y may be associated with nervous system manifestations in Fabry disease. J Neurol Sci. 2020;412:116757. - PubMed

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