"False"
Umeå universitet
printicon
Huvudmenyn dold.

Ann-Charloth Nilsson

Kontakt

E-post
lotta.nilsson@medbio.umu.se
Telefon
090-785 29 79

Verksam vid

Anknytning
Forskningsingenjör vid Institutionen för medicinsk biovetenskap Enhet: Klinisk kemi
Plats
By 6M, vån 2, Sjukhusområdet Umeå universitet, 901 85 Umeå
Association of NFE2L2 and KEAP1 haplotypes with amyotrophic lateral sclerosis
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Informa Healthcare 2014, Vol. 15, (1-2) : 130-137
Bergström, Petra; von Otter, Malin; Nilsson, Staffan; et al.
No GGGGCC-hexanucleotide repeat expansion in C9ORF72 in parkinsonism patients in Sweden
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, Informa Healthcare 2013, Vol. 14, (1) : 26-29
Akimoto, Chizuru; Forsgren, Lars; Linder, Jan; et al.
PGC-1 is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis
Human Molecular Genetics, Vol. 22, (17) : 3477-3484
Eschbach, Judith; Schwalenstocker, Birgit; Soyal, Selma M.; et al.
A novel SOD1 splice site mutation associated with familial ALS revealed by SOD activity analysis
Human Molecular Genetics, Vol. 19, (21) : 4201-4206
Birve, Anna; Neuwirth, Christoph; Weber, Markus; et al.
Visa publikationer i DiVA