Andersen PM - Search Results

1

Good practice in the management of amyotrophic lateral sclerosis: clinical guidelines. An evidence-based review with good practice points. EALSC Working Group.

Andersen PM, Borasio GD, Dengler R, Hardiman O, Kollewe K, Leigh PN, Pradat PF, Silani V, Tomik B; EALSC Working Group. Andersen PM, et al. Amyotroph Lateral Scler. 2007 Aug;8(4):195-213. doi: 10.1080/17482960701262376. Amyotroph Lateral Scler. 2007. PMID: 17653917 Review.

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

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

5

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

6

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

7

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.

8

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.

9

Genetics of sporadic ALS.

Andersen PM. Andersen PM. Amyotroph Lateral Scler Other Motor Neuron Disord. 2001 Mar;2 Suppl 1:S37-41. doi: 10.1080/14660820152415726. Amyotroph Lateral Scler Other Motor Neuron Disord. 2001. PMID: 11465923 Review.

10

The geographical and ethnic distribution of the D90A CuZn-SOD mutation in the Russian Federation.

Andersen PM, Spitsyn VA, Makarov SV, Nilsson L, Kravchuk OI, Bychkovskaya LS, Marklund SL. Andersen PM, et al. Amyotroph Lateral Scler Other Motor Neuron Disord. 2001 Jun;2(2):63-9. doi: 10.1080/146608201316949406. Amyotroph Lateral Scler Other Motor Neuron Disord. 2001. PMID: 11675874

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