Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Samuli Huttula"'
Autor:
Samuli Huttula, Henri Väyrynen, Seppo Helisalmi, Laura Kytövuori, Laura Luukkainen, Mikko Hiltunen, Anne M Remes, Johanna Krüger
Publikováno v:
Neurobiology of Aging. 114:113-116
Early-onset dementia (EOD) is highly heritable. However, in many EOD cases the genetic etiology remains unknown. Mitochondrial dysfunction is associated with neurodegeneration and the complex I (CI) deficiency is the most common enzyme deficiency in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9546128dfe748c927db9aba7bebf5f10
https://doi.org/10.1016/j.neurobiolaging.2021.09.026
https://doi.org/10.1016/j.neurobiolaging.2021.09.026
Autor:
Anne M. Remes, Mikko Hiltunen, Seppo Helisalmi, Henri Väyrynen, Johanna Krüger, Samuli Huttula, Laura Kytövuori, Laura Luukkainen, Annakaisa Haapasalo
Publikováno v:
Journal of Alzheimer's disease : JAD. 76(3)
BACKGROUND Alzheimer's disease, frontotemporal lobar degeneration, dementia with Lewy bodies, and Parkinson's disease (PD) overlap in clinical characteristics, neuropathology, and genetics. OBJECTIVE The aim of this study was to evaluate the role of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45c61f1a112ed53f8533f24e41f77b0f
https://pubmed.ncbi.nlm.nih.gov/32568194
https://pubmed.ncbi.nlm.nih.gov/32568194