Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Laura Luukkainen"'
Publikováno v:
Dementia and Geriatric Cognitive Disorders Extra, Vol 5, Iss 3, Pp 435-441 (2015)
Background: Frontotemporal lobar degeneration (FTLD) is responsible for as many as every fifth case of early-onset dementia. Very few epidemiological studies of FTLD have been conducted; there are no published epidemiological data of FTLD from Finlan
Externí odkaz:
https://doaj.org/article/f20f2796f9234ed6bc0615c3648b8b1e
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
Autor:
Anni-Kaisa Kähkönen, Laura Luukkainen
Publikováno v:
International Journal of Procurement Management. 1:1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a78a5a1354a41ed5662e2f30e1c6dddd
https://doi.org/10.1504/ijpm.2022.10040266
https://doi.org/10.1504/ijpm.2022.10040266
Autor:
Seppo Helisalmi, Mikko Hiltunen, Anne M. Remes, Johanna Krüger, Riitta Ahmasalo, Laura Kytövuori, Annakaisa Haapasalo, Laura Luukkainen, Eino Solje
Publikováno v:
Journal of Alzheimer's disease : JAD. 69(3)
A lot of effort has been done to unravel the genetics underlying early-onset Alzheimer's disease (AD) and frontotemporal lobar degeneration (FTLD). However, many familial early-onset dementia (EOD) cases still show an unclear genetic background. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23c79313901659a960662d6e3a2f1214
https://pubmed.ncbi.nlm.nih.gov/31127772
https://pubmed.ncbi.nlm.nih.gov/31127772
Publikováno v:
Dementia and Geriatric Cognitive Disorders EXTRA
Dementia and Geriatric Cognitive Disorders Extra, Vol 5, Iss 3, Pp 435-441 (2015)
Dementia and Geriatric Cognitive Disorders Extra, Vol 5, Iss 3, Pp 435-441 (2015)
Background: Frontotemporal lobar degeneration (FTLD) is responsible for as many as every fifth case of early-onset dementia. Very few epidemiological studies of FTLD have been conducted; there are no published epidemiological data of FTLD from Finlan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::641399eea72649a69afd97c3c705f329
http://europepmc.org/articles/PMC4677706
http://europepmc.org/articles/PMC4677706