Variably protease‐sensitive prionopathy presenting within ALS/FTD spectrum

We report clinico‐pathological features of a 65‐year‐old woman and a 56‐year‐old man with a 5‐year clinical history who had clinical and neuropathological characteristics of upper and lower motor neuron disease consistent with amyotrophic lateral sclerosis, and a frontotemporal atrophy pattern in ca...

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Detalles Bibliográficos
Autores principales: Vicente‐Pascual, Mikel, Rossi, Marcello, Gámez, Josep, Lladó, Albert, Valls, Josep, Grau‐Rivera, Oriol, Ávila Polo, Rainiero, Llorens, Franc, Zerr, Inga, Ferrer, Isidre, Nos, Carlos, Parchi, Piero, Sánchez‐Valle, Raquel, Gelpí, Ellen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Brief Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6186932/
https://www.ncbi.nlm.nih.gov/pubmed/30349865
http://dx.doi.org/10.1002/acn3.632

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6186932/
https://www.ncbi.nlm.nih.gov/pubmed/30349865
http://dx.doi.org/10.1002/acn3.632

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