McDermott CJ - Search Results

1

Clinical features of hereditary spastic paraplegia due to spastin mutation.

McDermott CJ, Burness CE, Kirby J, Cox LE, Rao DG, Hewamadduma C, Sharrack B, Hadjivassiliou M, Chinnery PF, Dalton A, Shaw PJ; UK and Irish HSP Consortium. McDermott CJ, et al. Neurology. 2006 Jul 11;67(1):45-51. doi: 10.1212/01.wnl.0000223315.62404.00. Neurology. 2006. PMID: 16832076

2

Hereditary spastic paraparesis: a review of new developments.

McDermott C, White K, Bushby K, Shaw P. McDermott C, et al. J Neurol Neurosurg Psychiatry. 2000 Aug;69(2):150-60. doi: 10.1136/jnnp.69.2.150. J Neurol Neurosurg Psychiatry. 2000. PMID: 10896685 Free PMC article. Review. No abstract available.

3

Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis.

Lindsey JC, Lusher ME, McDermott CJ, White KD, Reid E, Rubinsztein DC, Bashir R, Hazan J, Shaw PJ, Bushby KM. Lindsey JC, et al. Among authors: mcdermott cj. J Med Genet. 2000 Oct;37(10):759-65. doi: 10.1136/jmg.37.10.759. J Med Genet. 2000. PMID: 11015453 Free PMC article.

4

Paraplegin gene analysis in hereditary spastic paraparesis (HSP) pedigrees in northeast England.

McDermott CJ, Dayaratne RK, Tomkins J, Lusher ME, Lindsey JC, Johnson MA, Casari G, Turnbull DM, Bushby K, Shaw PJ. McDermott CJ, et al. Neurology. 2001 Feb 27;56(4):467-71. doi: 10.1212/wnl.56.4.467. Neurology. 2001. PMID: 11222789

5

Mutation screening of manganese superoxide dismutase in amyotrophic lateral sclerosis.

Tomkins J, Banner SJ, McDermott CJ, Shaw PJ. Tomkins J, et al. Among authors: mcdermott cj. Neuroreport. 2001 Aug 8;12(11):2319-22. doi: 10.1097/00001756-200108080-00008. Neuroreport. 2001. PMID: 11496103

6

Investigation of mitochondrial function in hereditary spastic paraparesis.

McDermott CJ, Taylor RW, Hayes C, Johnson M, Bushby KM, Turnbull DM, Shaw PJ. McDermott CJ, et al. Neuroreport. 2003 Mar 3;14(3):485-8. doi: 10.1097/00001756-200303030-00038. Neuroreport. 2003. PMID: 12634509

7

HSP60 is a rare cause of hereditary spastic paraparesis, but may act as a genetic modifier.

Hewamadduma CA, Kirby J, Kershaw C, Martindale J, Dalton A, McDermott CJ, Shaw PJ. Hewamadduma CA, et al. Among authors: mcdermott cj. Neurology. 2008 May 6;70(19):1717-8. doi: 10.1212/01.wnl.0000311395.31081.70. Neurology. 2008. PMID: 18458233 No abstract available.

8

New pedigrees and novel mutation expand the phenotype of REEP1-associated hereditary spastic paraplegia (HSP).

Hewamadduma C, McDermott C, Kirby J, Grierson A, Panayi M, Dalton A, Rajabally Y, Shaw P. Hewamadduma C, et al. Neurogenetics. 2009 Apr;10(2):105-10. doi: 10.1007/s10048-008-0163-z. Epub 2008 Nov 26. Neurogenetics. 2009. PMID: 19034539

9

An evaluation of neurophysiological criteria used in the diagnosis of motor neuron disease.

Douglass CP, Kandler RH, Shaw PJ, McDermott CJ. Douglass CP, et al. Among authors: mcdermott cj. J Neurol Neurosurg Psychiatry. 2010 Jun;81(6):646-9. doi: 10.1136/jnnp.2009.197434. J Neurol Neurosurg Psychiatry. 2010. PMID: 20522872 Clinical Trial.

10

Protocol for a double-blind randomised placebo-controlled trial of lithium carbonate in patients with amyotrophic lateral sclerosis (LiCALS) [Eudract number: 2008-006891-31].

Al-Chalabi A, Shaw PJ, Young CA, Morrison KE, Murphy C, Thornhill M, Kelly J, Steen IN, Leigh PN; UKMND-LiCALS. Al-Chalabi A, et al. BMC Neurol. 2011 Sep 21;11:111. doi: 10.1186/1471-2377-11-111. BMC Neurol. 2011. PMID: 21936930 Free PMC article. Clinical Trial.

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