Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Heidi Aaltokallio"'
Autor:
Eino Solje, Heidi Aaltokallio, Heli Koivumaa-Honkanen, Noora M Suhonen, Virpi Moilanen, Anna Kiviharju, Bryan Traynor, Pentti J Tienari, Päivi Hartikainen, Anne M Remes
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0131817 (2015)
The C9ORF72 expansion is one of the most common genetic etiologies observed with behavioural variant frontotemporal dementia (bvFTD). Revised diagnostic criteria for bvFTD (FTDC) were recently introduced but only a few studies have evaluated the accu
Externí odkaz:
https://doaj.org/article/df03e3f571a641ac93b3fa651e6e1eea
Autor:
Pentti J. Tienari, Anna Kiviharju, Bryan J. Traynor, Anne M. Remes, Eino Solje, Noora M. Suhonen, Heli Koivumaa-Honkanen, Heidi Aaltokallio, Päivi Hartikainen, Virpi Moilanen
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 7, p e0131817 (2015)
PLoS ONE, Vol 10, Iss 7, p e0131817 (2015)
Background The C9ORF72 expansion is one of the most common genetic etiologies observed with behavioural variant frontotemporal dementia (bvFTD). Revised diagnostic criteria for bvFTD (FTDC) were recently introduced but only a few studies have evaluat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7626108ca3da645a8fce65a07c27f31b
https://doi.org/10.1371/journal.pone.0131817
https://doi.org/10.1371/journal.pone.0131817