1. A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1–12q14. Issue 1 (5th January 2005) Authors: Wilkinson, P A; Simpson, M A; Bastaki, L; Patel, H; Reed, J A; Kalidas, K; Samilchuk, E; Khan, R; Warner, T T; Crosby, A H Journal: Journal of medical genetics Issue: Volume 42:Issue 1(2005) Page Start: 80 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Future of British psychiatrists. Issue 5789 (18th December 1971) Authors: Simpson, M A Journal: BMJ Issue: Volume 4:Issue 5789(1971) Page Start: 745 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the Amish. Issue 10 (8th May 2008) Authors: Zahka, K; Kalidas, K; Simpson, M A; Cross, H; Keller, B B; Galambos, C; Gurtz, K; Patton, M A; Crosby, A H Journal: Heart Issue: Volume 94:Issue 10(2008) Page Start: 1326 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Letter: An easy death--an uneasy argument. Issue 5976 (19th July 1975) Authors: Simpson, M A Journal: BMJ Issue: Volume 3:Issue 5976(1975) Page Start: 155 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Letter: Delayed drug-induced dystonias. Issue 5885 (20th October 1973) Authors: Simpson, M A Journal: BMJ Issue: Volume 4:Issue 5885(1973) Page Start: 174 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗