Ince PG - Search Results

1

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

2

Expression of vascular endothelial growth factor and its receptors in the central nervous system in amyotrophic lateral sclerosis.

Brockington A, Wharton SB, Fernando M, Gelsthorpe CH, Baxter L, Ince PG, Lewis CE, Shaw PJ. Brockington A, et al. Among authors: ince pg. J Neuropathol Exp Neurol. 2006 Jan;65(1):26-36. doi: 10.1097/01.jnen.0000196134.51217.74. J Neuropathol Exp Neurol. 2006. PMID: 16410746

3

Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation.

White KD, Ince PG, Lusher M, Lindsey J, Cookson M, Bashir R, Shaw PJ, Bushby KM. White KD, et al. Among authors: ince pg. Neurology. 2000 Jul 12;55(1):89-94. doi: 10.1212/wnl.55.1.89. Neurology. 2000. PMID: 10891911

4

Corticospinal tract degeneration in the progressive muscular atrophy variant of ALS.

Ince PG, Evans J, Knopp M, Forster G, Hamdalla HH, Wharton SB, Shaw PJ. Ince PG, et al. Neurology. 2003 Apr 22;60(8):1252-8. doi: 10.1212/01.wnl.0000058901.75728.4e. Neurology. 2003. PMID: 12707426

5

Amyotrophic lateral sclerosis associated with genetic abnormalities in the gene encoding Cu/Zn superoxide dismutase: molecular pathology of five new cases, and comparison with previous reports and 73 sporadic cases of ALS.

Ince PG, Tomkins J, Slade JY, Thatcher NM, Shaw PJ. Ince PG, et al. J Neuropathol Exp Neurol. 1998 Oct;57(10):895-904. doi: 10.1097/00005072-199810000-00002. J Neuropathol Exp Neurol. 1998. PMID: 9786240

6

Selective loss of neurofilament expression in Cu/Zn superoxide dismutase (SOD1) linked amyotrophic lateral sclerosis.

Menzies FM, Grierson AJ, Cookson MR, Heath PR, Tomkins J, Figlewicz DA, Ince PG, Shaw PJ. Menzies FM, et al. Among authors: ince pg. J Neurochem. 2002 Sep;82(5):1118-28. doi: 10.1046/j.1471-4159.2002.01045.x. J Neurochem. 2002. PMID: 12358759 Free article.

7

Expression of Ki67, PCNA and the chromosome replication licensing protein Mcm2 in glial cells of the ageing human hippocampus increases with the burden of Alzheimer-type pathology.

Wharton SB, Williams GH, Stoeber K, Gelsthorpe CH, Baxter L, Johnson AL, Ince PG; MRC-CFAS. Wharton SB, et al. Among authors: ince pg. Neurosci Lett. 2005 Jul 22-29;383(1-2):33-8. doi: 10.1016/j.neulet.2005.04.019. Epub 2005 Apr 26. Neurosci Lett. 2005. PMID: 15936508

8

Motor neuron disease in a patient with a mitochondrial tRNAIle mutation.

Borthwick GM, Taylor RW, Walls TJ, Tonska K, Taylor GA, Shaw PJ, Ince PG, Turnbull DM. Borthwick GM, et al. Among authors: ince pg. Ann Neurol. 2006 Mar;59(3):570-4. doi: 10.1002/ana.20758. Ann Neurol. 2006. PMID: 16358336

9

White matter lesions in an unselected cohort of the elderly: molecular pathology suggests origin from chronic hypoperfusion injury.

Fernando MS, Simpson JE, Matthews F, Brayne C, Lewis CE, Barber R, Kalaria RN, Forster G, Esteves F, Wharton SB, Shaw PJ, O'Brien JT, Ince PG; MRC Cognitive Function and Ageing Neuropathology Study Group. Fernando MS, et al. Among authors: ince pg. Stroke. 2006 Jun;37(6):1391-8. doi: 10.1161/01.STR.0000221308.94473.14. Epub 2006 Apr 20. Stroke. 2006. PMID: 16627790

10

Impairment of mitochondrial anti-oxidant defence in SOD1-related motor neuron injury and amelioration by ebselen.

Wood-Allum CA, Barber SC, Kirby J, Heath P, Holden H, Mead R, Higginbottom A, Allen S, Beaujeux T, Alexson SE, Ince PG, Shaw PJ. Wood-Allum CA, et al. Among authors: ince pg. Brain. 2006 Jul;129(Pt 7):1693-709. doi: 10.1093/brain/awl118. Epub 2006 May 15. Brain. 2006. PMID: 16702190

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