Editorial : Genotype–phenotype correlations in neurodegenerative diseases: From clinical features to neuroimaging signatures
(2022) In Frontiers in Neurology 13.
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/0c5f3407-2b4b-4435-b402-e65b794d6e6e
- author
- Ferraro, Pilar M. ; Spotorno, Nicola LU ; Finegan, Eoin ; Sampedro, Frederic and Caso, Francesca
- organization
- publishing date
- 2022-12
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- fragile X-associated tremor/ataxia syndrome, genetic, motor neuron diseases, multiple sclerosis, neurodegeneration, neuroimaging, progressive supranuclear palsy, Rett syndrome
- in
- Frontiers in Neurology
- volume
- 13
- article number
- 1100953
- publisher
- Frontiers Media S. A.
- external identifiers
-
- scopus:85145374854
- pmid:36588898
- ISSN
- 1664-2295
- DOI
- 10.3389/fneur.2022.1100953
- language
- English
- LU publication?
- yes
- id
- 0c5f3407-2b4b-4435-b402-e65b794d6e6e
- date added to LUP
- 2023-01-16 15:24:33
- date last changed
- 2024-09-19 11:03:10
@misc{0c5f3407-2b4b-4435-b402-e65b794d6e6e, author = {{Ferraro, Pilar M. and Spotorno, Nicola and Finegan, Eoin and Sampedro, Frederic and Caso, Francesca}}, issn = {{1664-2295}}, keywords = {{fragile X-associated tremor/ataxia syndrome; genetic; motor neuron diseases; multiple sclerosis; neurodegeneration; neuroimaging; progressive supranuclear palsy; Rett syndrome}}, language = {{eng}}, publisher = {{Frontiers Media S. A.}}, series = {{Frontiers in Neurology}}, title = {{Editorial : Genotype–phenotype correlations in neurodegenerative diseases: From clinical features to neuroimaging signatures}}, url = {{http://dx.doi.org/10.3389/fneur.2022.1100953}}, doi = {{10.3389/fneur.2022.1100953}}, volume = {{13}}, year = {{2022}}, }