1. 69 THE PRADER-WILLI CLINICAL SUBPHENOTYPE OF FRAGILE X SYNDROME. (1st January 2006) Authors: Nowicki, S. T.; Tassone, F.; Ferranti, J.; Ono, M. Y.; Hagerman, R. J. Journal: Journal of investigative medicine Issue: Volume 54:Number 1(2006) Page Start: S91 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A family with two female siblings with compound heterozygous FMR1 premutation alleles. (28th July 2013) Authors: Basuta, K.; Lozano, R.; Schneider, A.; Yrigollen, C.M.; Hessl, D.; Hagerman, R.J.; Tassone, F. Journal: Clinical genetics Issue: Volume 85:Number 5(2014:May) Page Start: 458 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Broad autism spectrum and obsessive–compulsive symptoms in adults with the fragile X premutation. Issue 6 (17th August 2016) Authors: Schneider, A.; Johnston, C.; Tassone, F.; Sansone, S.; Hagerman, R. J.; Ferrer, E.; Rivera, S. M.; Hessl, D. Journal: Clinical neuropsychologist Issue: Volume 30:Issue 6(2016) Page Start: 929 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cutaneous adverse reactions following SARS‐CoV‐2 vaccine booster dose: a real‐life multicentre experience. (10th July 2022) Authors: Avallone, G.; Cavallo, F.; Astrua, C.; Caldarola, G.; Conforti, C.; De Simone, C.; di Meo, N.; di Stefani, A.; Genovese, G.; Maronese, C.A.; Marzano, A.V.; Parente, R.; Quaglino, P.; Roccuzzo, G.; Tassone, F.; Zalaudek, I.; Senetta, R.; Ribero, S. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 36:Number 11(2022) Page Start: e876 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. FXTAS in an unmethylated mosaic male with fragile X syndrome from Chile. (13th October 2013) Authors: Santa María, L.; Pugin, A.; Alliende, M.A.; Aliaga, S.; Curotto, B.; Aravena, T.; Tang, H.‐T.; Mendoza‐Morales, G.; Hagerman, R.; Tassone, F. Journal: Clinical genetics Issue: Volume 86:Number 4(2014:Oct.) Page Start: 378 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Metformin as targeted treatment in fragile X syndrome. Issue 2 (25th September 2017) Authors: Dy, A.B.C.; Tassone, F.; Eldeeb, M.; Salcedo‐Arellano, M.J.; Tartaglia, N.; Hagerman, R. Journal: Clinical genetics Issue: Volume 93:Issue 2(2018) Page Start: 216 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Psychological status in female carriers of premutation FMR1 allele showing a complex relationship with the size of CGG expansion. (17th February 2014) Authors: Loesch, D. Z.; Bui, M. Q.; Hammersley, E.; Schneider, A.; Storey, E.; Stimpson, P.; Burgess, T.; Francis, D.; Slater, H.; Tassone, F.; Hagerman, R. J.; Hessl, D. Journal: Clinical genetics Issue: Volume 87:Number 2(2015:Feb.) Page Start: 173 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Tacrolimus 0.1% ointment in nail psoriasis: a randomized controlled open‐label study. (13th July 2012) Authors: De Simone, C.; Maiorino, A.; Tassone, F.; D'Agostino, M.; Caldarola, G. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 27:Number 8(2013:Aug.) Page Start: 1003 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗