Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Editorial
. 2021 Mar;28(3):733-734.
doi: 10.1111/ene.14694. Epub 2021 Jan 6.

Hypomyelinating leukodystrophies in adults

Affiliations
Editorial

Hypomyelinating leukodystrophies in adults

Fanny Mochel. Eur J Neurol. 2021 Mar.
No abstract available

PubMed Disclaimer

Comment on

  • Hypomyelinating leukodystrophies in adults: Clinical and genetic features.
    Di Bella D, Magri S, Benzoni C, Farina L, Maccagnano C, Sarto E, Moscatelli M, Baratta S, Ciano C, Piacentini SHMJ, Draghi L, Mauro E, Pareyson D, Gellera C, Taroni F, Salsano E. Di Bella D, et al. Eur J Neurol. 2021 Mar;28(3):934-944. doi: 10.1111/ene.14646. Epub 2020 Dec 3. Eur J Neurol. 2021. PMID: 33190326

References

REFERENCES

    1. van der Knaap MS, Schiffmann R, Mochel F, Wolf NI. Diagnosis, prognosis, and treatment of leukodystrophies. Lancet Neurol. 2019;18(10):962-972. https://doi.org/10.1016/S1474-4422(19)30143-7
    1. Lynch DS, Wade C, Paiva ARB, et al. Practical approach to the diagnosis of adult-onset leukodystrophies: an updated guide in the genomic era. J Neurol Neurosurg Psychiatry. 2019;90(5):543-554. https://doi.org/10.1136/jnnp-2018-319481
    1. Di Bella D, Magri S, Benzoni C, et al. Hypomyelinating leukodystrophies in adults: clinical and genetic features. Eur J Neurol. 2020; 28: 934-944. https://doi.org/10.1111/ene.14646
    1. Rubegni A, Battisti C, Tessa A, et al. SPG2 mimicking multiple sclerosis in a family identified using next generation sequencing. J Neurol Sci. 2017;375:198-202. https://doi.org/10.1016/j.jns.2017.01.069
    1. Kuipers DJS, Tufekcioglu Z, Bilgiç B, et al. Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish family. Parkinsonism Relat Disord. 2019;66:228-231. https://doi.org/10.1016/j.parkreldis.2019.07.033

LinkOut - more resources