1. A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changes. Issue 3 (5th December 2007) Authors: Loesch, D Z; Cook, M; Litewka, L; Gould, E; Churchyard, A; Tassone, F; Slater, H R; Storey, E Journal: Journal of medical genetics Issue: Volume 45:Issue 3(2008) Page Start: 179 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1messenger RNA. Issue 7 (1st July 2001) Authors: Tassone, F; Hagerman, R J; Taylor, A K; Hagerman, P J Journal: Journal of medical genetics Issue: Volume 38:Issue 7(2001) Page Start: 453 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. FMR1 premutation in females diagnosed with multiple sclerosis. Issue 7 (16th June 2009) Authors: Zhang, L; Coffey, S; Lua, L L; Greco, C M; Schafer, J A; Brunberg, J; Borodyanskaya, M; Agius, M A; Apperson, M; Leehey, M; Tartaglia, N; Tassone, F; Hagerman, P J; Hagerman, R J Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 80:Issue 7(2009) Page Start: 812 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Fragile X‐associated tremor/ataxia syndrome (FXTAS) in grey zone carriers. (17th October 2012) Authors: Liu, Y; Winarni, TI; Zhang, L; Tassone, F; Hagerman, RJ Journal: Clinical genetics Issue: Volume 84:Number 1(2013:Jul.) Page Start: 74 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome. Issue 4 (1st April 2004) Authors: Tassone, F; Hagerman, R J; Garcia-Arocena, D; Khandjian, E W; Greco, C M; Hagerman, P J Journal: Journal of medical genetics Issue: Volume 41:Issue 4(2004) Page Start: e43 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's disease. (25th December 2012) Authors: Loesch, DZ; Tassone, F; Lo, J; Slater, HR; Hills, LV; Bui, MQ; Silburn, PA; Mellick, GD Journal: Clinical genetics Issue: Volume 84:Number 4(2013:Oct.) Page Start: 382 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Offering fragile X syndrome carrier screening: a prospective mixed-methods observational study comparing carrier screening of pregnant and non-pregnant women in the general population. Issue 9 (9th September 2013) Authors: Martyn, M; Anderson, V; Archibald, A; Carter, R; Cohen, J; Delatycki, M; Donath, S; Emery, J; Halliday, J; Hill, M; Sheffield, L; Slater, H; Tassone, F; Younie, S; Metcalfe, S Journal: BMJ open Issue: Volume 3:Issue 9(2013) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Prevalence and risk of migraine headaches in adult fragile X premutation carriers. (21st February 2013) Authors: Au, J; Akins, RS; Berkowitz‐Sutherland, L; Tang, H‐T; Chen, Y; Boyd, A; Tassone, F; Nguyen, DV; Hagerman, R Journal: Clinical genetics Issue: Volume 84:Number 6(2013:Dec.) Page Start: 546 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Spastic paraparesis, cerebellar ataxia, and intention tremor: a severe variant of FXTAS?. Issue 2 (2nd February 2005) Authors: Jacquemont, S; Orrico, A; Galli, L; Sahota, P K; Brunberg, J A; Anichini, C; Leehey, M; Schaeffer, S; Hagerman, R J; Hagerman, P J; Tassone, F Journal: Journal of medical genetics Issue: Volume 42:Issue 2(2005) Page Start: e14 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗