Publications

Author

Title

Year sorteringsordning

Fulltext

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

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Eschbach, Judith
Schwalenstocker, Birgit
Soyal, Selma M.; et al.

PGC-1 is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis
Human Molecular Genetics, 22(17): 3477-3484

2013

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Akimoto, Chizuru
Forsgren, Lars
Linder, Jan; et al.

No GGGGCC-hexanucleotide repeat expansion in C9ORF72 in parkinsonism patients in Sweden
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 14(1): 26-29

2013

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Birve, Anna
Neuwirth, Christoph
Weber, Markus; et al.

A novel SOD1 splice site mutation associated with familial ALS revealed by SOD activity analysis
Human Molecular Genetics, 19(21): 4201-4206

2010

-


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