Shaw PJ - Search Results

1

Concurrence of multiple sclerosis and amyotrophic lateral sclerosis in patients with hexanucleotide repeat expansions of C9ORF72.

Ismail A, Cooper-Knock J, Highley JR, Milano A, Kirby J, Goodall E, Lowe J, Scott I, Constantinescu CS, Walters SJ, Price S, McDermott CJ, Sawcer S, Compston DA, Sharrack B, Shaw PJ. Ismail A, et al. Among authors: shaw pj. J Neurol Neurosurg Psychiatry. 2013 Jan;84(1):79-87. doi: 10.1136/jnnp-2012-303326. Epub 2012 Oct 20. J Neurol Neurosurg Psychiatry. 2013. PMID: 23085936

2

Mitochondrial involvement in amyotrophic lateral sclerosis.

Menzies FM, Ince PG, Shaw PJ. Menzies FM, et al. Among authors: shaw pj. Neurochem Int. 2002 May;40(6):543-51. doi: 10.1016/s0197-0186(01)00125-5. Neurochem Int. 2002. PMID: 11850111 Review.

3

Mitochondrial dysfunction in a cell culture model of familial amyotrophic lateral sclerosis.

Menzies FM, Cookson MR, Taylor RW, Turnbull DM, Chrzanowska-Lightowlers ZM, Dong L, Figlewicz DA, Shaw PJ. Menzies FM, et al. Among authors: shaw pj. Brain. 2002 Jul;125(Pt 7):1522-33. doi: 10.1093/brain/awf167. Brain. 2002. PMID: 12077002

4

Differential gene expression in a cell culture model of SOD1-related familial motor neurone disease.

Kirby J, Menzies FM, Cookson MR, Bushby K, Shaw PJ. Kirby J, et al. Among authors: shaw pj. Hum Mol Genet. 2002 Aug 15;11(17):2061-75. doi: 10.1093/hmg/11.17.2061. Hum Mol Genet. 2002. PMID: 12165567

5

Update on the glutamatergic neurotransmitter system and the role of excitotoxicity in amyotrophic lateral sclerosis.

Heath PR, Shaw PJ. Heath PR, et al. Among authors: shaw pj. Muscle Nerve. 2002 Oct;26(4):438-58. doi: 10.1002/mus.10186. Muscle Nerve. 2002. PMID: 12362409 Review.

6

Hereditary spastic paraplegia.

McDermott CJ, Shaw PJ. McDermott CJ, et al. Among authors: shaw pj. 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.

7

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. Among authors: shaw pj. 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

8

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: shaw pj. J Neuropathol Exp Neurol. 2003 Nov;62(11):1166-77. doi: 10.1093/jnen/62.11.1166. J Neuropathol Exp Neurol. 2003. PMID: 14656074

9

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. Among authors: shaw pj. Ann Neurol. 2003 Dec;54(6):748-59. doi: 10.1002/ana.10757. Ann Neurol. 2003. PMID: 14681884

10

Screening of the regulatory and coding regions of vascular endothelial growth factor in amyotrophic lateral sclerosis.

Brockington A, Kirby J, Eggitt D, Schofield E, Morris C, Lewis CE, Ince PG, Shaw PJ. Brockington A, et al. Among authors: shaw pj. Neurogenetics. 2005 May;6(2):101-4. doi: 10.1007/s10048-004-0201-4. Epub 2005 Mar 18. Neurogenetics. 2005. PMID: 15776280 No abstract available.

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