Monogenic small vessel diseases - rare but still important
- PMID: 32355255
- DOI: 10.1038/s41582-020-0363-1
Monogenic small vessel diseases - rare but still important
Comment on
-
Monogenic cerebral small-vessel diseases: diagnosis and therapy. Consensus recommendations of the European Academy of Neurology.Eur J Neurol. 2020 Jun;27(6):909-927. doi: 10.1111/ene.14183. Epub 2020 Mar 20. Eur J Neurol. 2020. PMID: 32196841
References
-
- Tan, R. Y. Y. et al. How common are single gene mutations as a cause for lacunar stroke? A targeted gene panel study. Neurology 93, e2007–e2020 (2019). - DOI
-
- Tournier-Lasserve, E. et al. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Nat. Genet. 3, 256–259 (1993). - DOI
-
- Carare, R. O., Hawkes, C. A., Jeffrey, M., Kalaria, R. N. & Weller, R. O. Review: cerebral amyloid angiopathy, prion angiopathy, CADASIL and the spectrum of protein elimination failure angiopathies (PEFA) in neurodegenerative disease with a focus on therapy. Neuropathol. Appl. Neurobiol. 39, 593–611 (2013). - DOI
-
- Mancuso, M. et al. Monogenic cerebral small-vessel diseases: diagnosis and therapy. Consensus recommendations of the European Academy of Neurology. Eur. J. Neurol. https://doi.org/10.1111/ene.14183 (2020). - DOI - PubMed
-
- van der Knaap, M. S., Schiffmann, R., Mochel, F. & Wolf, N. I. Diagnosis, prognosis, and treatment of leukodystrophies. Lancet Neurol. 18, 962–972 (2019). - DOI
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
