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

Ferraro, Pilar M; Spotorno, Nicola; Finegan, Eoin; Sampedro, Frederic; Caso, Francesca

Ferraro, Pilar M; Spotorno, Nicola; Finegan, Eoin; Sampedro, Frederic; Caso, Francesca.

Afiliação

Ferraro PM; Neurology Unit, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Spotorno N; Clinical Memory Research Unit, Department of Clinical Sciences, Malmö, Lund University, Lund, Sweden.
Finegan E; Computational Neuroimaging Group, Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland.
Sampedro F; Movement Disorders Unit, Neurology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Caso F; Biomedical Research Institute (IIB-Sant Pau), Barcelona, Spain.

Front Neurol ; 13: 1100953, 2022.

Article em En | MEDLINE | ID: mdl-36588898

Palavras-chave

Rett syndrome; fragile X-associated tremor/ataxia syndrome; genetic; motor neuron diseases; multiple sclerosis; neurodegeneration; neuroimaging; progressive supranuclear palsy

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article