Powell JF - Search Results

1

Copper and zinc levels in familial amyotrophic lateral sclerosis patients with CuZnSOD gene mutations.

Radunović A, Delves HT, Robberecht W, Tilkin P, Enayat ZE, Shaw CE, Stević Z, Apostolski S, Powell JF, Leigh PN. Radunović A, et al. Among authors: powell jf. Ann Neurol. 1997 Jul;42(1):130-1. doi: 10.1002/ana.410420124. Ann Neurol. 1997. PMID: 9225698 No abstract available.

2

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. Among authors: powell jf. Ann Neurol. 2001 May;49(5):643-9. Ann Neurol. 2001. PMID: 11357955

3

Familial amyotrophic lateral sclerosis. Molecular pathology of a patient with a SOD1 mutation.

Shaw CE, Enayat ZE, Powell JF, Anderson VE, Radunovic A, al-Sarraj S, Leigh PN. Shaw CE, et al. Among authors: powell jf. Neurology. 1997 Dec;49(6):1612-6. doi: 10.1212/wnl.49.6.1612. Neurology. 1997. PMID: 9409355

4

Mutations in all five exons of SOD-1 may cause ALS.

Shaw CE, Enayat ZE, Chioza BA, Al-Chalabi A, Radunovic A, Powell JF, Leigh PN. Shaw CE, et al. Among authors: powell jf. Ann Neurol. 1998 Mar;43(3):390-4. doi: 10.1002/ana.410430319. Ann Neurol. 1998. PMID: 9506558

5

Mutations in the lysyl oxidase gene are not associated with amyotrophic lateral sclerosis.

Chioza BA, Ujfalusy A, Csiszar K, Leigh PN, Powell JF, Radunović A. Chioza BA, et al. Among authors: powell jf. Amyotroph Lateral Scler Other Motor Neuron Disord. 2001 Jun;2(2):93-7. doi: 10.1080/146608201316949532. Amyotroph Lateral Scler Other Motor Neuron Disord. 2001. PMID: 11675877

6

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: powell jf. Hum Mol Genet. 1999 Feb;8(2):157-64. doi: 10.1093/hmg/8.2.157. Hum Mol Genet. 1999. PMID: 9931323

7

No association of the SOD1 locus and disease susceptibility or phenotype in sporadic ALS.

Broom WJ, Parton MJ, Vance CA, Russ C, Andersen PM, Hansen V, Leigh PN, Powell JF, Al-Chalabi A, Shaw CE. Broom WJ, et al. Among authors: powell jf. Neurology. 2004 Dec 28;63(12):2419-22. doi: 10.1212/01.wnl.0000147264.60349.eb. Neurology. 2004. PMID: 15623718

8

Neurofilaments, free radicals, excitotoxins, and amyotrophic lateral sclerosis.

al-Chalabi A, Powell JF, Leigh PN. al-Chalabi A, et al. Among authors: powell jf. Muscle Nerve. 1995 May;18(5):540-5. doi: 10.1002/mus.880180511. Muscle Nerve. 1995. PMID: 7739643 Review.

9

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.

Shatunov A, Mok K, Newhouse S, Weale ME, Smith B, Vance C, Johnson L, Veldink JH, van Es MA, van den Berg LH, Robberecht W, Van Damme P, Hardiman O, Farmer AE, Lewis CM, Butler AW, Abel O, Andersen PM, Fogh I, Silani V, Chiò A, Traynor BJ, Melki J, Meininger V, Landers JE, McGuffin P, Glass JD, Pall H, Leigh PN, Hardy J, Brown RH Jr, Powell JF, Orrell RW, Morrison KE, Shaw PJ, Shaw CE, Al-Chalabi A. Shatunov A, et al. Among authors: powell jf. Lancet Neurol. 2010 Oct;9(10):986-94. doi: 10.1016/S1474-4422(10)70197-6. Lancet Neurol. 2010. PMID: 20801717 Free PMC article.

10

Variants in the ALS2 gene are not associated with sporadic amyotrophic lateral sclerosis.

Al-Chalabi A, Hansen VK, Simpson CL, Xi J, Hosler BA, Powell JF, McKenna-Yasek D, Shaw CE, Leigh PN, Brown RH Jr. Al-Chalabi A, et al. Among authors: powell jf. Neurogenetics. 2003 Aug;4(4):221-2. doi: 10.1007/s10048-003-0152-1. Epub 2003 May 27. Neurogenetics. 2003. PMID: 12768434 No abstract available.

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