Andersen P - Search Results

1

A novel ALS SOD1 C6S mutation with implications for aggregation related toxicity and genetic counseling.

Brotherton T, Polak M, Kelly C, Birve A, Andersen P, Marklund SL, Glass JD. Brotherton T, et al. Among authors: andersen p. Amyotroph Lateral Scler. 2011 May;12(3):215-9. doi: 10.3109/17482968.2010.531279. Epub 2010 Nov 12. Amyotroph Lateral Scler. 2011. PMID: 21073275

2

Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase.

Andersen PM, Nilsson P, Ala-Hurula V, Keränen ML, Tarvainen I, Haltia T, Nilsson L, Binzer M, Forsgren L, Marklund SL. Andersen PM, et al. Nat Genet. 1995 May;10(1):61-6. doi: 10.1038/ng0595-61. Nat Genet. 1995. PMID: 7647793

3

Autosomal recessive adult-onset amyotrophic lateral sclerosis associated with homozygosity for Asp90Ala CuZn-superoxide dismutase mutation. A clinical and genealogical study of 36 patients.

Andersen PM, Forsgren L, Binzer M, Nilsson P, Ala-Hurula V, Keränen ML, Bergmark L, Saarinen A, Haltia T, Tarvainen I, Kinnunen E, Udd B, Marklund SL. Andersen PM, et al. Brain. 1996 Aug;119 ( Pt 4):1153-72. doi: 10.1093/brain/119.4.1153. Brain. 1996. PMID: 8813280

4

Normal binding and reactivity of copper in mutant superoxide dismutase isolated from amyotrophic lateral sclerosis patients.

Marklund SL, Andersen PM, Forsgren L, Nilsson P, Ohlsson PI, Wikander G, Oberg A. Marklund SL, et al. Among authors: andersen pm. J Neurochem. 1997 Aug;69(2):675-81. doi: 10.1046/j.1471-4159.1997.69020675.x. J Neurochem. 1997. PMID: 9231727 Free article.

5

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. Brain. 1997 Oct;120 ( Pt 10):1723-37. doi: 10.1093/brain/120.10.1723. Brain. 1997. PMID: 9365366

6

CuZn-superoxide dismutase, extracellular superoxide dismutase, and glutathione peroxidase in blood from individuals homozygous for Asp90Ala CuZu-superoxide dismutase mutation.

Andersen PM, Nilsson P, Forsgren L, Marklund SL. Andersen PM, et al. J Neurochem. 1998 Feb;70(2):715-20. doi: 10.1046/j.1471-4159.1998.70020715.x. J Neurochem. 1998. PMID: 9453566 Free article.

7

Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factor.

Al-Chalabi A, Andersen PM, Chioza B, Shaw C, Sham PC, Robberecht W, Matthijs G, Camu W, Marklund SL, Forsgren L, Rouleau G, Laing NG, Hurse PV, Siddique T, Leigh PN, Powell JF. Al-Chalabi A, et al. Among authors: andersen pm. Hum Mol Genet. 1998 Dec;7(13):2045-50. doi: 10.1093/hmg/7.13.2045. Hum Mol Genet. 1998. PMID: 9817920

8

[Familial amyotrophic lateral sclerosis].

Keränen ML, Ala-Hurula VM, Saarinen A, Andersen PM, Marklund SL. Keränen ML, et al. Among authors: andersen pm. Duodecim. 1996;112(21):2026-30. Duodecim. 1996. PMID: 10605205 Finnish. No abstract available.

9

Superoxide dismutase in CSF from amyotrophic lateral sclerosis patients with and without CuZn-superoxide dismutase mutations.

Jacobsson J, Jonsson PA, Andersen PM, Forsgren L, Marklund SL. Jacobsson J, et al. Among authors: andersen pm. Brain. 2001 Jul;124(Pt 7):1461-6. doi: 10.1093/brain/124.7.1461. Brain. 2001. PMID: 11408340 Clinical Trial.

10

Genetic factors in the early diagnosis of ALS.

Andersen PM. Andersen PM. Amyotroph Lateral Scler Other Motor Neuron Disord. 2000 Mar;1 Suppl 1:S31-42. doi: 10.1080/14660820052415899. Amyotroph Lateral Scler Other Motor Neuron Disord. 2000. PMID: 11464924 Review.

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