1. 1118 Are MND patients pre-morbidly fitter? Indirect evidence from hospital record-linkage. Issue 3 (9th February 2012) Authors: Turner, M; Wotton, C; Talbot, K; Goldacre, M J Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 83:Issue 3(2012) Page Start: e1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 169 Antisaccade task as a biomarker in MND. Issue 3 (9th February 2012) Authors: Sharma, R; Hicks, S; Berna, C; Kennard, C; Talbot, K; Turner, M R Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 83:Issue 3(2012) Page Start: e1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Amyotrophic lateral sclerosis, 2nd edn. Issue 1 (15th December 2006) Authors: Talbot, K Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 78:Issue 1(2007) Page Start: 109 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Asymmetrical late onset motor neuropathy associated with a novel mutation in the small heat shock protein HSPB1 (HSP27). Issue 4 (14th March 2008) Authors: James, P A; Rankin, J; Talbot, K Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 79:Issue 4(2008) Page Start: 461 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Concordance between site of onset and limb dominance in amyotrophic lateral sclerosis. Issue 8 (18th June 2010) Authors: Turner, M R; Wicks, P; Brownstein, C A; Massagli, M P; Toronjo, M; Talbot, K; Al-Chalabi, A Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 82:Issue 8(2011) Page Start: 853 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Evidence for compound heterozygosity causing mild and severe forms of autosomal recessive spinal muscular atrophy. Issue 12 (December 1996) Authors: Talbot, K; Rodrigues, N; Bernert, G; Bittner, R; Davies, K Journal: Journal of medical genetics Issue: Volume 33:Issue 12(1996) Page Start: 1019 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Functional vitamin B12 deficiency. Issue 1 (16th January 2009) Authors: Turner, M R; Talbot, K Journal: Practical neurology Issue: Volume 9:Issue 1(2009) Page Start: 37 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Gene deletions in spinal muscular atrophy. Issue 2 (February 1996) Authors: Rodrigues, N R; Owen, N; Talbot, K; Patel, S; Muntoni, F; Ignatius, J; Dubowitz, V; Davies, K E Journal: Journal of medical genetics Issue: Volume 33:Issue 2(1996) Page Start: 93 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Motor neurone disease. Issue 923 (1st September 2002) Authors: Talbot, K Journal: Postgraduate medical journal Issue: Volume 78:Issue 923(2002) Page Start: 513 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. PATH44 Corpus callosum diffusion tensor imaging as a biomarker for motor neurone disease. Issue 11 (22nd October 2010) Authors: Filippini, N; Douaud, G; Mackay, C E; Knight, S; Talbot, K; Turner, M R Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 81:Issue 11(2010) Page Start: e19 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗