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Peter Andersen

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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

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

Wnt and Extraocular Muscle Sparing in Amyotrophic Lateral Sclerosis.
Investigative ophthalmology & visual science

2014

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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

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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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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

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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

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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

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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

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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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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

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Sidansvarig: Åsa Nordström
2014-06-02

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