Gredal O - Search Results

1

Novel TARDBP mutations in Nordic ALS patients.

Chiang HH, Andersen PM, Tysnes OB, Gredal O, Christensen PB, Graff C. Chiang HH, et al. Among authors: gredal o. J Hum Genet. 2012 May;57(5):316-9. doi: 10.1038/jhg.2012.24. Epub 2012 Mar 29. J Hum Genet. 2012. PMID: 22456481

2

Ataxin-2 intermediate-length polyglutamine expansions in European ALS patients.

Lee T, Li YR, Ingre C, Weber M, Grehl T, Gredal O, de Carvalho M, Meyer T, Tysnes OB, Auburger G, Gispert S, Bonini NM, Andersen PM, Gitler AD. Lee T, et al. Among authors: gredal o. Hum Mol Genet. 2011 May 1;20(9):1697-700. doi: 10.1093/hmg/ddr045. Epub 2011 Feb 3. Hum Mol Genet. 2011. PMID: 21292779 Free PMC article.

3

Inclusions of amyotrophic lateral sclerosis-linked superoxide dismutase in ventral horns, liver, and kidney.

Jonsson PA, Bergemalm D, Andersen PM, Gredal O, Brännström T, Marklund SL. Jonsson PA, et al. Among authors: gredal o. Ann Neurol. 2008 May;63(5):671-5. doi: 10.1002/ana.21356. Ann Neurol. 2008. PMID: 18409196

4

Phenotypic heterogeneity in motor neuron disease patients with CuZn-superoxide dismutase mutations in Scandinavia.

Andersen PM, Nilsson P, Keränen ML, Forsgren L, Hägglund J, Karlsborg M, Ronnevi LO, Gredal O, Marklund SL. Andersen PM, et al. Among authors: gredal o. Brain. 1997 Oct;120 ( Pt 10):1723-37. doi: 10.1093/brain/120.10.1723. Brain. 1997. PMID: 9365366

5

Minute quantities of misfolded mutant superoxide dismutase-1 cause amyotrophic lateral sclerosis.

Jonsson PA, Ernhill K, Andersen PM, Bergemalm D, Brännström T, Gredal O, Nilsson P, Marklund SL. Jonsson PA, et al. Among authors: gredal o. Brain. 2004 Jan;127(Pt 1):73-88. doi: 10.1093/brain/awh005. Epub 2003 Oct 8. Brain. 2004. PMID: 14534160

6

[Amyotrophic lateral sclerosis and superoxide dismutase--a review].

Binzer MN, Gredal O, Brøndum-Nielsen K, Andersen PM. Binzer MN, et al. Among authors: gredal o. Ugeskr Laeger. 1997 Mar 10;159(11):1593-6. Ugeskr Laeger. 1997. PMID: 9092140 Review. Danish.

7

Toxicity of familial ALS-linked SOD1 mutants from selective recruitment to spinal mitochondria.

Liu J, Lillo C, Jonsson PA, Vande Velde C, Ward CM, Miller TM, Subramaniam JR, Rothstein JD, Marklund S, Andersen PM, Brännström T, Gredal O, Wong PC, Williams DS, Cleveland DW. Liu J, et al. Among authors: gredal o. Neuron. 2004 Jul 8;43(1):5-17. doi: 10.1016/j.neuron.2004.06.016. Neuron. 2004. PMID: 15233913 Free article.

8

A clinical trial of dextromethorphan in amyotrophic lateral sclerosis.

Gredal O, Werdelin L, Bak S, Christensen PB, Boysen G, Kristensen MO, Jespersen JH, Regeur L, Hinge HH, Jensen TS. Gredal O, et al. Acta Neurol Scand. 1997 Jul;96(1):8-13. doi: 10.1111/j.1600-0404.1997.tb00231.x. Acta Neurol Scand. 1997. PMID: 9262126 Clinical Trial.

9

Human CCS gene: genomic organization and exclusion as a candidate for amyotrophic lateral sclerosis (ALS).

Silahtaroglu AN, Brondum-Nielsen K, Gredal O, Werdelin L, Panas M, Petersen MB, Tommerup N, Tümer Z. Silahtaroglu AN, et al. Among authors: gredal o. BMC Genet. 2002 Apr 19;3:5. doi: 10.1186/1471-2156-3-5. BMC Genet. 2002. PMID: 11991808 Free PMC article.

10

Novel heterozygous nonsense mutation of the OPTN gene segregating in a Danish family with ALS.

Tümer Z, Bertelsen B, Gredal O, Magyari M, Nielsen KC, Lucamp, Grønskov K, Brøndum-Nielsen K. Tümer Z, et al. Among authors: gredal o. Neurobiol Aging. 2012 Jan;33(1):208.e1-5. doi: 10.1016/j.neurobiolaging.2011.07.001. Epub 2011 Aug 26. Neurobiol Aging. 2012. PMID: 21852022

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