Shaw PJ - Search Results

1

C9ORF72 expansions, parkinsonism, and Parkinson disease: a clinicopathologic study.

Cooper-Knock J, Frolov A, Highley JR, Charlesworth G, Kirby J, Milano A, Hartley J, Ince PG, McDermott CJ, Lashley T, Revesz T, Shaw PJ, Wood NW, Bandmann O. Cooper-Knock J, et al. Among authors: shaw pj. Neurology. 2013 Aug 27;81(9):808-11. doi: 10.1212/WNL.0b013e3182a2cc38. Epub 2013 Jul 24. Neurology. 2013. PMID: 23884045 Free PMC article.

2

Parvalbumin and calbindin D-28k in the human motor system and in motor neuron disease.

Ince P, Stout N, Shaw P, Slade J, Hunziker W, Heizmann CW, Baimbridge KG. Ince P, et al. Neuropathol Appl Neurobiol. 1993 Aug;19(4):291-9. doi: 10.1111/j.1365-2990.1993.tb00443.x. Neuropathol Appl Neurobiol. 1993. PMID: 8232749

3

The expression of the glutamate re-uptake transporter excitatory amino acid transporter 1 (EAAT1) in the normal human CNS and in motor neurone disease: an immunohistochemical study.

Banner SJ, Fray AE, Ince PG, Steward M, Cookson MR, Shaw PJ. Banner SJ, et al. Among authors: shaw pj. Neuroscience. 2002;109(1):27-44. doi: 10.1016/s0306-4522(01)00437-7. Neuroscience. 2002. PMID: 11784698

4

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.

5

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

6

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

7

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: shaw pj. J Neurochem. 2002 Sep;82(5):1118-28. doi: 10.1046/j.1471-4159.2002.01045.x. J Neurochem. 2002. PMID: 12358759 Free article.

8

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.

9

No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disorders.

Ahmad-Annuar A, Shah P, Hafezparast M, Hummerich H, Witherden AS, Morrison KE, Shaw PJ, Kirby J, Warner TT, Crosby A, Proukakis C, Wilkinson P, Orrell RW, Bradley L, Martin JE, Fisher EM. Ahmad-Annuar A, et al. Among authors: shaw pj. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Sep;4(3):150-7. doi: 10.1080/14660820310011737. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003. PMID: 13129801

10

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

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