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Page 1
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.
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.
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.
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.
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.
181 results