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Editorial : Genotype–phenotype correlations in neurodegenerative diseases: From clinical features to neuroimaging signatures

Ferraro, Pilar M. ; Spotorno, Nicola LU ; Finegan, Eoin ; Sampedro, Frederic and Caso, Francesca (2022) In Frontiers in Neurology 13.
Please use this url to cite or link to this publication:
author
; ; ; and
organization
publishing date
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
2024-05-30 00:56:01
@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}},
}