Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jenny Björkström"'
Autor:
Håkan Thonberg, Huei-Hsin Chiang, Lena Lilius, Charlotte Forsell, Anna-Karin Lindström, Charlotte Johansson, Jenny Björkström, Steinunn Thordardottir, Kristel Sleegers, Christine Van Broeckhoven, Annica Rönnbäck, Caroline Graff
Publikováno v:
Acta Neuropathologica Communications, Vol 5, Iss 1, Pp 1-14 (2017)
Abstract Alzheimer disease (AD) is a progressive neurodegenerative disorder and the most common form of dementia. The majority of AD cases are sporadic, while up to 5% are families with an early onset AD (EOAD). Mutations in one of the three genes: a
Externí odkaz:
https://doaj.org/article/c59c108dc0284f3baaa06cab13de6805
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:
Charlotte Johansson, Annica Rönnbäck, Anna-Karin Lindström, Huei-Hsin Chiang, Kristel Sleegers, Håkan Thonberg, Steinunn Thordardottir, Lena Lilius, Christine Van Broeckhoven, Caroline Graff, Charlotte Forsell, Jenny Björkström
Publikováno v:
Acta Neuropathologica Communications
Acta Neuropathologica Communications, Vol 5, Iss 1, Pp 1-14 (2017)
Acta neuropathologica communications
Acta Neuropathologica Communications, Vol 5, Iss 1, Pp 1-14 (2017)
Acta neuropathologica communications
Alzheimer disease (AD) is a progressive neurodegenerative disorder and the most common form of dementia. The majority of AD cases are sporadic, while up to 5% are families with an early onset AD (EOAD). Mutations in one of the three genes: amyloid be
Autor:
Inger Nennesmo, Jenny Björkström, Håkan Thonberg, Marie Fallström, Caroline Graff, Jacqueline Schoumans
Publikováno v:
BMC Research Notes, vol. 4, no. 476, pp. 1-9
BMC Research Notes
BMC Research Notes, Vol 4, Iss 1, p 476 (2011)
BMC Research Notes
BMC Research Notes, Vol 4, Iss 1, p 476 (2011)
Background Missense mutations in three different genes encoding amyloid-β precursor protein, presenilin 1 and presenilin 2 are recognized to cause familial early-onset Alzheimer disease. Also duplications of the amyloid precursor protein gene have b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fcee63692bc32870e3857d14870a11d
https://serval.unil.ch/notice/serval:BIB_2B21B4515D23
https://serval.unil.ch/notice/serval:BIB_2B21B4515D23