Shaw C - 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: shaw c, shaw pj. 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

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. Among authors: shaw c. 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

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

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. Among authors: shaw c. 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

Hereditary pure lower motor neuron disease with adult onset and rapid progression.

Van den Berg-Vos RM, Van den Berg LH, Jansen GH, Parton M, Shaw CE, Hesseling-Janssen AL, Wokke JH. Van den Berg-Vos RM, et al. Among authors: shaw ce. J Neurol. 2001 Apr;248(4):290-6. doi: 10.1007/s004150170203. J Neurol. 2001. PMID: 11374093

10

Compound heterozygosity and variable penetrance in SOD1 amyotrophic lateral sclerosis pedigrees.

Parton MJ, Andersen PM, Broom WJ, Shaw CE. Parton MJ, et al. Among authors: shaw ce. Ann Neurol. 2001 Oct;50(4):553-4. doi: 10.1002/ana.1151. Ann Neurol. 2001. PMID: 11601511 No abstract available.

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