1. Comparison of X‐chromosome inactivation in Duchenne muscle/myocardium‐manifesting carriers, non‐manifesting carriers and related daughters. (20th December 2012) Authors: Viggiano, E; Picillo, E; Cirillo, A; Politano, L Journal: Clinical genetics Issue: Volume 84:Number 3(2013:Sep.) Page Start: 265 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes. Issue 9 (1st September 2005) Authors: Piluso, G; Politano, L; Aurino, S; Fanin, M; Ricci, E; Ventriglia, V M; Belsito, A; Totaro, A; Saccone, V; Topaloglu, H; Nascimbeni, A C; Fulizio, L; Broccolini, A; Canki-Klain, N; Comi, L I; Nigro, G; Angelini, C; Nigro, V Journal: Journal of medical genetics Issue: Volume 42:Issue 9(2005) Page Start: 686 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Is heart rate variability a valid parameter to predict sudden death in patients with Becker's muscular dystrophy?. Issue 11 (13th October 2006) Authors: Ammendola, E; Russo, V; Politano, L; Santangelo, L; Calabrò, R Journal: Heart Issue: Volume 92:Issue 11(2006) Page Start: 1686 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Is the value of QT dispersion a valid method to foresee the risk of sudden death? A study in Becker patients. Issue 2 (1st February 2002) Authors: Nigro, Ge; Nigro, G; Politano, L; Santangelo, L; Petretta, V R; Passamano, L; Panico, F; De Luca, F; Montefusco, A; Comi, L I Journal: Heart Issue: Volume 87:Issue 2(2002) Page Start: 156 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes. Issue 12 (18th December 2003) Authors: Vytopil, M; Benedetti, S; Ricci, E; Galluzzi, G; Dello Russo, A; Merlini, L; Boriani, G; Gallina, M; Morandi, L; Politano, L; Moggio, M; Chiveri, L; Hausmanova-Petrusewicz, I; Ricotti, R; Vohanka, S; Toman, J; Toniolo, D Journal: Journal of medical genetics Issue: Volume 40:Issue 12(2003) Page Start: e132 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. P3170Innovative approach for risk stratification of LMNA-related cardiomyopathy: results from an integrated cardiological and neurological 10-year follow-up multicentre study. (28th August 2018) Authors: Peretto, G; Di Resta, C; Perversi, J; Forleo, C; Maggi, L; Previtali, S; Politano, L; Manzi, R C; D'Amico, A; Limongelli, G; Ambrosi, A; Ferrari, M; Della Bella, P; Sala, S; Benedetti, S Journal: European heart journal Issue: Volume 39(2018)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Phenotype and clinical outcomes of dystrophin associated dilated cardiomyopathy. (25th November 2020) Authors: Restrepo Cordoba, M.A; Wahbi, K; Florian, A; Mogensen, J; Jimenez-Jaimez, J; Climent-Paya, V; Politano, L; Garcia-Alvarez, A; Arad, M; Barriales-Villa, R; Kubanek, M; Lopes, L.R; Jurcut, R; Hazebroek, M.R; Garcia-Pavia, P Journal: European heart journal Issue: Volume 41:(2020)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Risk of arrhythmia in type I myotonic dystrophy: the role of clinical and genetic variables. Issue 7 (22nd February 2009) Authors: Cudia, P; Bernasconi, P; Chiodelli, R; Mangiola, F; Bellocci, F; Russo, A Dello; Angelini, C; Romeo, V; Melacini, P; Politano, L; Palladino, A; Nigro, G; Siciliano, G; Falorni, M; Bongiorni, M G; Falcone, C; Mantegazza, R; Morandi, L Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 80:Issue 7(2009) Page Start: 790 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗