Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Charlotte, Forsell"'
Autor:
Huei-Hsin Chiang, Linn Öijerstedt, Anna-Karin Lindström, Charlotte Forsell, Caroline Graff, Lena Lilius, Håkan Thonberg, Jenny Björkström
Publikováno v:
Neurobiology of Aging. 84:241.e21-241.e25
Frontotemporal dementia (FTD) is the second most common early-onset dementia. Up to half of the cases are familial, and several mutations have been identified as pathogenic. Repeat expansion mutations in C9orf72 are the most common genetic cause of F
Autor:
Latchezar Traykov, Lena Lilius, Bengt Winblad, Håkan Thonberg, Eric Westman, Shima Mehrabian, Katya Stoyanova, Charlotte Forsell, Desislava Nesheva, Caroline Graff, Draga Toncheva, Margarita Raycheva, Lena Cavallin
Publikováno v:
PLoS ONE, Vol 13, Iss 12, p e0208383 (2018)
PLoS ONE
PLoS ONE
Background The GGGGCC repeat expansion in the C9orf72 gene was recently identified as a major cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) in several European populations. The objective of this study was to determine
Autor:
Lena Lilius, Linn Öijerstedt, Inger Nennesmo, Marie Westerlund, Håkan Thonberg, Huei-Hsin Chiang, Steinunn Thordardottir, Caroline Graff, Krishnan Shanmugarajan, Charlotte Forsell
Frontotemporal lobar degeneration (FTLD) is a progressive neurodegenerative disease with an age at onset generally below 65 years. Mutations in progranulin (GRN) have been reported to be able to cause FTLD through haploinsufficiency. We have sequence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c940f85cbaf1435096f0547fd6ff70f5
https://europepmc.org/articles/PMC3798842/
https://europepmc.org/articles/PMC3798842/
Publikováno v:
Alzheimer's & Dementia. 6
significant variants (P
Autor:
Susanne Froelich Fabre, Lars-Olof Wahlund, Marie Blomberg, Matti Viitanen, Christian Andersen, Anders Wallin, Charlotte Forsell, Kaj Blennow, Lars Lannfelt, Magnus Sjögren
Publikováno v:
Experimental neurology. 168(2)
Frontotemporal dementia (FTD) belongs to a group of neurodegenerative disorders known as tauopathies, characterized by intracellular aggregation of hyperphosphorylated tau protein in the brain. Some tauopathies, like Alzheimer's disease (AD), consist
Autor:
Charlotte Forsell, Hans Basun, Lena Lilius, Susanne Froelich, Karin Axelman, Athena Andreadis, Lars Lannfelt
Publikováno v:
American journal of medical genetics. 74(4)
Familial frontotemporal dementia (FTD) is a complex disorder with lack of distinctive histopathological markers found in other types of dementia. Most of the linkage reports from FTD families map the disease loci to chromosome 17q21-22. However, FTD
Autor:
Lars-Olof Wahlund, Arne Brun, Hans Basun, Lars Lannfelt, Susanne Froelich, John Collinge, Tracy Campbell, Charlotte Forsell, Lennart Wetterberg, Karin Axelman, Ove Almkvist
Publikováno v:
Karolinska Institutet
Objective: To describe symptoms, signs, neuroimaging results, and neuropathologic findings in patients from a family with chromosome 17q21—linked autosomal dominant frontotemporal dementia. Design: Multiple case report with genetic investigations.