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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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Van Doormaal, Perry T. C.
Ticozzi, Nicola
Gellera, Cinzia; et al.

Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study
Neurobiology of Aging, 35(10): 2420.e13-

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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Diekstra, Frank P.
Van Deerlin, Vivianna M.
van Swieten, John C.; et al.

C9orf72 and UNC13A Are Shared Risk Loci for Amyotrophic Lateral Sclerosis and Frontotemporal Dementia: A Genome-Wide Meta-Analysis
Annals of Neurology, 76(1): 120-133

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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Sidansvarig: Åsa Nordström
2014-06-02

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