Structural MRI Signatures in Genetic Presentations of the Frontotemporal Dementia/Motor Neuron Disease Spectrum

BACKGROUND AND OBJECTIVES: To assess cortical, subcortical, and cerebellar gray matter (GM) atrophy using MRI in patients with disorders of the frontotemporal lobar degeneration (FTLD) spectrum with known genetic mutations. METHODS: Sixty-six patients carrying FTLD-related mutations were enrolled, i...

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Detalles Bibliográficos
Autores principales: Spinelli, Edoardo Gioele, Ghirelli, Alma, Basaia, Silvia, Cividini, Camilla, Riva, Nilo, Canu, Elisa, Castelnovo, Veronica, Domi, Teuta, Magnani, Giuseppe, Caso, Francesca, Caroppo, Paola, Prioni, Sara, Rossi, Giacomina, Tremolizzo, Lucio, Appollonio, Ildebrando, Silani, Vincenzo, Carrera, Paola, Filippi, Massimo, Agosta, Federica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8548958/
https://www.ncbi.nlm.nih.gov/pubmed/34544819
http://dx.doi.org/10.1212/WNL.0000000000012702

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8548958/
https://www.ncbi.nlm.nih.gov/pubmed/34544819
http://dx.doi.org/10.1212/WNL.0000000000012702

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