Till umu.se

Publikationer

Författare

Titel

År sorteringsordning

Fulltext

Bergh, Johan
Zetterström, Per
Andersen, Peter M.; et al.

Structural and kinetic analysis of protein-aggregate strains in vivo using binary epitope mapping
Proceedings of the National Academy of Sciences of the United States of America, 112(14): 4489-4494

2015

-

Freischmidt, Axel
Wieland, Thomas
Richter, Benjamin; et al.

Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia
Nature Neuroscience, 18(5): 631-+

2015

-

Nordin, Angelica
Akimoto, Chizuru
Wuolikainen, Anna; et al.

Extensive size variability of the GGGGCC expansion in C9orf72 in both neuronal and non-neuronal tissues in 18 patients with ALS or FTD
Human Molecular Genetics, 24(11): 3133-3142

2015

-

Goris, An
van Setten, Jessica
Diekstra, Frank; et al.

No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis
Human Molecular Genetics, 23(7): 1916-1922

2014

-

McLoon, Linda K
Harandi, Vahid M
Brännstrom, Thomas; et al.

Wnt and Extraocular Muscle Sparing in Amyotrophic Lateral Sclerosis
Investigative ophthalmology & visual science, 55: 5482-5496

2014

-

Freischmidt, Axel
Mueller, Kathrin
Zondler, Lisa; et al.

Serum microRNAs in patients with genetic amyotrophic lateral sclerosis and pre-manifest mutation carriers
Brain, 137(11): 2938-2950

2014

-

Van Doormaal, Perry T. C.
Ticozzi, Nicola
Gellera, Cinzia; et al.

Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study
Neurobiology of Aging, 35(10): 2420.e13-

2014

-

Wuolikainen, Anna
Acimovic, Jure
Loevgren-Sandblom, Anita; et al.

Cholesterol, Oxysterol, Triglyceride, and Coenzyme Q Homeostasis in ALS. Evidence against the Hypothesis That Elevated 27-Hydroxycholesterol Is a Pathogenic Factor
PLoS ONE, 9(11): e113619-

2014

Hämta

Akimoto, Chizuru
Volk, Alexander E.
van Blitterswijk, Marka; et al.

A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories
Journal of Medical Genetics, 51(6): 419-424

2014

-

Bergström, Petra
von Otter, Malin
Nilsson, Staffan; et al.

Association of NFE2L2 and KEAP1 haplotypes with amyotrophic lateral sclerosis
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 15(1-2): 130-137

2014

-


Sidansvarig: Åsa Nordström
2014-06-02

Utskriftsversion