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Case report: coexistence of C9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia—clinical features and neuroimaging correlates

Detalles Bibliográficos
Autores principales: Ghirelli, Alma, Spinelli, Edoardo Gioele, Canu, Elisa, Domi, Teuta, Basaia, Silvia, Castelnovo, Veronica, Pozzi, Laura, Magnani, Giuseppe, Caso, Francesca, Caroppo, Paola, Prioni, Sara, Villa, Cristina, Riva, Nilo, Quattrini, Angelo, Carrera, Paola, Filippi, Massimo, Agosta, Federica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511558/
https://www.ncbi.nlm.nih.gov/pubmed/37382630
http://dx.doi.org/10.1007/s00415-023-11839-3
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author Ghirelli, Alma
Spinelli, Edoardo Gioele
Canu, Elisa
Domi, Teuta
Basaia, Silvia
Castelnovo, Veronica
Pozzi, Laura
Magnani, Giuseppe
Caso, Francesca
Caroppo, Paola
Prioni, Sara
Villa, Cristina
Riva, Nilo
Quattrini, Angelo
Carrera, Paola
Filippi, Massimo
Agosta, Federica
author_facet Ghirelli, Alma
Spinelli, Edoardo Gioele
Canu, Elisa
Domi, Teuta
Basaia, Silvia
Castelnovo, Veronica
Pozzi, Laura
Magnani, Giuseppe
Caso, Francesca
Caroppo, Paola
Prioni, Sara
Villa, Cristina
Riva, Nilo
Quattrini, Angelo
Carrera, Paola
Filippi, Massimo
Agosta, Federica
author_sort Ghirelli, Alma
collection PubMed
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spelling pubmed-105115582023-09-22 Case report: coexistence of C9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia—clinical features and neuroimaging correlates Ghirelli, Alma Spinelli, Edoardo Gioele Canu, Elisa Domi, Teuta Basaia, Silvia Castelnovo, Veronica Pozzi, Laura Magnani, Giuseppe Caso, Francesca Caroppo, Paola Prioni, Sara Villa, Cristina Riva, Nilo Quattrini, Angelo Carrera, Paola Filippi, Massimo Agosta, Federica J Neurol Letter to the Editors Springer Berlin Heidelberg 2023-06-29 2023 /pmc/articles/PMC10511558/ /pubmed/37382630 http://dx.doi.org/10.1007/s00415-023-11839-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Letter to the Editors
Ghirelli, Alma
Spinelli, Edoardo Gioele
Canu, Elisa
Domi, Teuta
Basaia, Silvia
Castelnovo, Veronica
Pozzi, Laura
Magnani, Giuseppe
Caso, Francesca
Caroppo, Paola
Prioni, Sara
Villa, Cristina
Riva, Nilo
Quattrini, Angelo
Carrera, Paola
Filippi, Massimo
Agosta, Federica
Case report: coexistence of C9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia—clinical features and neuroimaging correlates
title Case report: coexistence of C9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia—clinical features and neuroimaging correlates
title_full Case report: coexistence of C9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia—clinical features and neuroimaging correlates
title_fullStr Case report: coexistence of C9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia—clinical features and neuroimaging correlates
title_full_unstemmed Case report: coexistence of C9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia—clinical features and neuroimaging correlates
title_short Case report: coexistence of C9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia—clinical features and neuroimaging correlates
title_sort case report: coexistence of c9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia—clinical features and neuroimaging correlates
topic Letter to the Editors
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511558/
https://www.ncbi.nlm.nih.gov/pubmed/37382630
http://dx.doi.org/10.1007/s00415-023-11839-3
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