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Peter Andersen

Kontaktinformation

Befattning:

Professor/överläkare

personbild

Verksam vid:

Farmakologi och klinisk neurovetenskap

Avdelning:

Klinisk neurovetenskap

Adress:

Umeå universitet
SE-901 85 Umeå
Sverige

Besöksadress:

Byggnad 6B, 6H och 10, NUS

Tel:

+46 90 785 23 72

E-postadress:

peter.andersen@neuro.umu.seE-post

Webbsida:

http://www.neuropharm.umu.se Webbsida

Publikationer

Författare

Titel

År 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

-

Rosenbohm, Angela
Kassubek, Jan
Weydt, Patrick; et al.

Can lesions to the motor cortex induce amyotrophic lateral sclerosis?
Journal of Neurology, 261(2): 283-290

2014

-

Fogh, Isabella
Ratti, Antonia
Gellera, Cinzia; et al.

A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis
Human Molecular Genetics, 23(8): 2220-2231

2014

-

Czell, David
Andersen, Peter M
Neuwirth, Christoph; et al.

Progressive aphasia as the presenting symptom in a patient with amyotrophic lateral sclerosis with a novel mutation in the OPTN gene
Amyotrophic Lateral Sclerosis and Frontootemporal Degeneration, 14(2): 138-140

2013

-

Ingre, Caroline
Landers, John E
Rizik, Naji; et al.

A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts
Neurobiology of Aging, 34(6): 1708.e1-1708.e6

2013

-

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

-

van Rheenen, Wouter
Diekstra, Frank P
van Doormaal, Perry TC; et al.

H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis
Neurobiology of Aging, 34(5): 1517.e5-1517.e7

2013

-

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

-

Ingre, Caroline
Pinto, Susana
Birve, Anna; et al.

No association between VAPB mutations and familial or sporadic ALS in Sweden, Portugal and Iceland
Amyotrophic lateral sclerosis and frontotemporal degeneration, 14(7-8): 620-627

2013

-

Weishaupt, Jochen H
Waibel, Stefan
Birve, Anna; et al.

A novel optineurin truncating mutation and three glaucoma-associated missense variants in patients with familial amyotrophic lateral sclerosis in Germany
Neurobiology of Aging, 34(5): 1516.e9-1516.e15

2013

-


Sidansvarig: Agneta Valleskog
2010-11-02

Utskriftsversion