Andersen PM - Search Results

1

Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: increased susceptibility in male carriers of the -2578AA genotype.

Lambrechts D, Poesen K, Fernández-Santiago R, Al-Chalabi A, Del Bo R, Van Vught PW, Khan S, Marklund SL, Brockington A, van Marion I, Anneser J, Shaw C, Ludolph AC, Leigh NP, Comi GP, Gasser T, Shaw PJ, Morrison KE, Andersen PM, Van den Berg LH, Thijs V, Siddique T, Robberecht W, Carmeliet P. Lambrechts D, et al. Among authors: andersen pm. J Med Genet. 2009 Dec;46(12):840-6. doi: 10.1136/jmg.2008.058222. Epub 2008 Apr 15. J Med Genet. 2009. PMID: 18413368

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

Deletions of the heavy neurofilament subunit tail in amyotrophic lateral sclerosis.

Al-Chalabi A, Andersen PM, Nilsson P, Chioza B, Andersson JL, Russ C, Shaw CE, Powell JF, Leigh PN. Al-Chalabi A, et al. Among authors: andersen pm. Hum Mol Genet. 1999 Feb;8(2):157-64. doi: 10.1093/hmg/8.2.157. Hum Mol Genet. 1999. PMID: 9931323

9

[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.

10

Intron 7 retention and exon 9 skipping EAAT2 mRNA variants are not associated with amyotrophic lateral sclerosis.

Flowers JM, Powell JF, Leigh PN, Andersen P, Shaw CE. Flowers JM, et al. Ann Neurol. 2001 May;49(5):643-9. Ann Neurol. 2001. PMID: 11357955

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