Shaw CE - Search Results

1

Homozygosity analysis in amyotrophic lateral sclerosis.

Mok K, Laaksovirta H, Tienari PJ, Peuralinna T, Myllykangas L, Chiò A, Traynor BJ, Nalls MA, Gurunlian N, Shatunov A, Restagno G, Mora G, Nigel Leigh P, Shaw CE, Morrison KE, Shaw PJ, Al-Chalabi A, Hardy J, Orrell RW. Mok K, et al. Among authors: shaw ce, shaw pj. Eur J Hum Genet. 2013 Dec;21(12):1429-35. doi: 10.1038/ejhg.2013.59. Epub 2013 Apr 24. Eur J Hum Genet. 2013. PMID: 23612577 Free PMC article.

2

Two novel mutations in the gene for copper zinc superoxide dismutase in UK families with amyotrophic lateral sclerosis.

Enayat ZE, Orrell RW, Claus A, Ludolph A, Bachus R, Brockmüller J, Ray-Chaudhuri K, Radunovic A, Shaw C, Wilkinson J, et al. Enayat ZE, et al. Hum Mol Genet. 1995 Jul;4(7):1239-40. doi: 10.1093/hmg/4.7.1239. Hum Mol Genet. 1995. PMID: 8528216 No abstract available.

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. 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. Ann Neurol. 1998 Mar;43(3):390-4. doi: 10.1002/ana.410430319. Ann Neurol. 1998. PMID: 9506558

5

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. Hum Mol Genet. 1998 Dec;7(13):2045-50. doi: 10.1093/hmg/7.13.2045. Hum Mol Genet. 1998. PMID: 9817920

6

Flail arm syndrome: a distinctive variant of amyotrophic lateral sclerosis.

Hu MT, Ellis CM, Al-Chalabi A, Leigh PN, Shaw CE. Hu MT, et al. Among authors: shaw ce. J Neurol Neurosurg Psychiatry. 1998 Dec;65(6):950-1. doi: 10.1136/jnnp.65.6.950. J Neurol Neurosurg Psychiatry. 1998. PMID: 9854987 Free PMC article. No abstract available.

7

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

8

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: shaw ce. Ann Neurol. 2001 May;49(5):643-9. Ann Neurol. 2001. PMID: 11357955

9

Progress in the pathogenesis of amyotrophic lateral sclerosis.

Shaw CE, al-Chalabi A, Leigh N. Shaw CE, et al. Curr Neurol Neurosci Rep. 2001 Jan;1(1):69-76. doi: 10.1007/s11910-001-0078-7. Curr Neurol Neurosci Rep. 2001. PMID: 11898502 Review.

10

Prognostic modelling of therapeutic interventions in amyotrophic lateral sclerosis.

Turner MR, Bakker M, Sham P, Shaw CE, Leigh PN, Al-Chalabi A. Turner MR, et al. Among authors: shaw ce. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002 Mar;3(1):15-21. doi: 10.1080/146608202317576499. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002. PMID: 12061944

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