Shaw CE - Search Results

1

[11C]-WAY100635 PET demonstrates marked 5-HT1A receptor changes in sporadic ALS.

Turner MR, Rabiner EA, Hammers A, Al-Chalabi A, Grasby PM, Shaw CE, Brooks DJ, Leigh PN. Turner MR, et al. Among authors: shaw ce. Brain. 2005 Apr;128(Pt 4):896-905. doi: 10.1093/brain/awh428. Epub 2005 Feb 2. Brain. 2005. PMID: 15689356

2

Association of apolipoprotein E epsilon 4 allele with bulbar-onset motor neuron disease.

al-Chalabi A, Enayat ZE, Bakker MC, Sham PC, Ball DM, Shaw CE, Lloyd CM, Powell JF, Leigh PN. al-Chalabi A, et al. Among authors: shaw ce. Lancet. 1996 Jan 20;347(8995):159-60. doi: 10.1016/s0140-6736(96)90343-8. Lancet. 1996. PMID: 8544551

3

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: shaw ce. Ann Neurol. 1997 Jul;42(1):130-1. doi: 10.1002/ana.410420124. Ann Neurol. 1997. PMID: 9225698 No abstract available.

4

CuZnSOD-associated amyotrophic lateral sclerosis.

Radunović A, Shaw CE, Akman-Demir G, Idrisoglu H, Leigh PN. Radunović A, et al. Among authors: shaw ce. Ann Neurol. 1997 Aug;42(2):273-4. doi: 10.1002/ana.410420229. Ann Neurol. 1997. PMID: 9266745 No abstract available.

5

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

6

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

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

8

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.

9

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

10

Use of human intravenous immunoglobulin in lower motor neuron syndromes.

Ellis CM, Leary S, Payan J, Shaw C, Hu M, O'Brien M, Leigh PN. Ellis CM, et al. J Neurol Neurosurg Psychiatry. 1999 Jul;67(1):15-9. doi: 10.1136/jnnp.67.1.15. J Neurol Neurosurg Psychiatry. 1999. PMID: 10369816 Free PMC article.

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