McDermott CJ - Search Results

1

Physical activity as an exogenous risk factor in motor neuron disease (MND): a review of the evidence.

Harwood CA, McDermott CJ, Shaw PJ. Harwood CA, et al. Among authors: mcdermott cj. Amyotroph Lateral Scler. 2009 Aug;10(4):191-204. doi: 10.1080/17482960802549739. Amyotroph Lateral Scler. 2009. PMID: 19263258 Review.

2

Hereditary spastic paraplegia.

McDermott CJ, Shaw PJ. McDermott CJ, et al. Int Rev Neurobiol. 2002;53:191-204. doi: 10.1016/s0074-7742(02)53008-7. Int Rev Neurobiol. 2002. PMID: 12512341 Review. No abstract available.

3

Spastin and paraplegin gene analysis in selected cases of motor neurone disease (MND).

McDermott CJ, Roberts D, Tomkins J, Bushby KM, Shaw PJ. McDermott CJ, et al. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Jun;4(2):96-9. doi: 10.1080/14660820310012718. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003. PMID: 14506940

4

The cellular and molecular pathology of the motor system in hereditary spastic paraparesis due to mutation of the spastin gene.

Wharton SB, McDermott CJ, Grierson AJ, Wood JD, Gelsthorpe C, Ince PG, Shaw PJ. Wharton SB, et al. Among authors: mcdermott cj. J Neuropathol Exp Neurol. 2003 Nov;62(11):1166-77. doi: 10.1093/jnen/62.11.1166. J Neuropathol Exp Neurol. 2003. PMID: 14656074

5

Hereditary spastic paraparesis: disrupted intracellular transport associated with spastin mutation.

McDermott CJ, Grierson AJ, Wood JD, Bingley M, Wharton SB, Bushby KM, Shaw PJ. McDermott CJ, et al. Ann Neurol. 2003 Dec;54(6):748-59. doi: 10.1002/ana.10757. Ann Neurol. 2003. PMID: 14681884

6

The microtubule-severing protein Spastin is essential for axon outgrowth in the zebrafish embryo.

Wood JD, Landers JA, Bingley M, McDermott CJ, Thomas-McArthur V, Gleadall LJ, Shaw PJ, Cunliffe VT. Wood JD, et al. Among authors: mcdermott cj. Hum Mol Genet. 2006 Sep 15;15(18):2763-71. doi: 10.1093/hmg/ddl212. Epub 2006 Aug 7. Hum Mol Genet. 2006. PMID: 16893913

7

Linkage to a known gene but no mutation identified: comprehensive reanalysis of SPG4 HSP pedigrees reveals large deletions as the sole cause.

Beetz C, Zuchner S, Ashley-Koch A, Auer-Grumbach M, Byrne P, Chinnery PF, Hutchinson M, McDermott CJ, Meijer IA, Nygren AO, Pericak-Vance M, Pyle A, Rouleau GA, Schickel J, Shaw PJ, Deufel T. Beetz C, et al. Among authors: mcdermott cj. Hum Mutat. 2007 Jul;28(7):739-40. doi: 10.1002/humu.20508. Hum Mutat. 2007. PMID: 17345589 No abstract available.

8

Diagnosis and management of motor neurone disease.

McDermott CJ, Shaw PJ. McDermott CJ, et al. BMJ. 2008 Mar 22;336(7645):658-62. doi: 10.1136/bmj.39493.511759.BE. BMJ. 2008. PMID: 18356234 Free PMC article. Review. No abstract available.

9

Chapter 17 Hereditary spastic paraparesis.

McDermott CJ, Shaw PJ. McDermott CJ, et al. Handb Clin Neurol. 2007;82:327-52. doi: 10.1016/S0072-9752(07)80020-0. Handb Clin Neurol. 2007. PMID: 18808902 No abstract available.

10

Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients.

Kasher PR, De Vos KJ, Wharton SB, Manser C, Bennett EJ, Bingley M, Wood JD, Milner R, McDermott CJ, Miller CC, Shaw PJ, Grierson AJ. Kasher PR, et al. Among authors: mcdermott cj. J Neurochem. 2009 Jul;110(1):34-44. doi: 10.1111/j.1471-4159.2009.06104.x. Epub 2009 Apr 22. J Neurochem. 2009. PMID: 19453301 Free article.

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