Till umu.se

Peter Andersen

Klinisk neurovetenskap

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Freischmidt, Axel
Mueller, Kathrin
Ludolph, Albert C.; et al.

Association of Mutations in TBK1 With Sporadic and Familial Amyotrophic Lateral Sclerosis and Frontotemporal Dementia
JAMA Neurology, 74(1): 110-113

2017

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Benatar, Michael
Stanislaw, Christine
Reyes, Eliana; et al.

Presymptomatic ALS genetic counseling and testing: Experience and recommendations
Neurology, 86(24): 2295-2302

2016

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Kenna, Kevin P.
van Doormaal, Perry T. C.
Dekker, Annelot M.; et al.

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
Nature Genetics, 48(9): 1037-1042

2016

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Wuolikainen, Anna
Jonsson, Pär
Ahnlund, Maria; et al.

Multi-platform mass spectrometry analysis of the CSF and plasma metabolomes of rigorously matched amyotrophic lateral sclerosis, Parkinson's disease and control subjects
Molecular Biosystems, 12(4): 1287-1298

2016

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Menke, Ricarda A. L.
Proudfoot, Malcolm
Wuu, Joanne; et al.

Increased functional connectivity common to symptomatic amyotrophic lateral sclerosis and those at genetic risk
Journal of Neurology, Neurosurgery and Psychiatry, 87(6): 580-588

2016

Hämta

Oeckl, Patrick
Jardel, Claude
Salachas, Francois; et al.

Multicenter validation of CSF neurofilaments as diagnostic biomarkers for ALS
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 17(5-6): 404-413

2016

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Tjust, Anton E.
Danielsson, Adam
Andersen, Peter M.; et al.

Loss of myofibers containing MyHC Slow tonic in extraocular muscles of terminal ALS patients with bulbar onset
Investigative Ophthalmology and Visual Science, 57(12)

2016

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Brenner, David
Andersen, Peter M.
Ludolph, Albert C.; et al.

Comment on "Cutting Edge: Inhibiting TBK1 by Compound II Ameliorates Autoimmune Disease in Mice"
Journal of Immunology, 196(2): 530-

2016

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Brenner, David
Mueller, Kathrin
Wieland, Thomas; et al.

NEK1 mutations in familial amyotrophic lateral sclerosis
Brain, 139: CP14-CP17

2016

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van Rheenen, Wouter
Shatunov, Aleksey
Dekker, Annelot M.; et al.

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
Nature Genetics, 48(9): 1043-1048

2016

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Sidansvarig: Åsa Nordström

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