1. Cross‐sectional serum metabolomic study of multiple forms of muscular dystrophy. Issue 4 (14th February 2018) Authors: Spitali, Pietro; Hettne, Kristina; Tsonaka, Roula; Sabir, Ekrem; Seyer, Alexandre; Hemerik, Jesse B.A.; Goeman, Jelle J.; Picillo, Esther; Ergoli, Manuela; Politano, Luisa; Aartsma‐Rus, Annemieke Journal: Journal of cellular and molecular medicine Issue: Volume 22:Issue 4(2018) Page Start: 2442 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Skewed X‐chromosome inactivation plays a crucial role in the onset of symptoms in carriers of Becker muscular dystrophy. (April 2017) Authors: Viggiano, Emanuela; Picillo, Esther; Ergoli, Manuela; Cirillo, Alessandra; Del Gaudio, Stefania; Politano, Luisa Journal: Journal of gene medicine Issue: Volume 19:Number 4(2017) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Study of expression of genes potentially responsible for reduced fitness in patients with myotonic dystrophy type 1 and identification of new biomarkers of testicular function. Issue 1 (16th December 2019) Authors: Ergoli, Manuela; Venditti, Massimo; Picillo, Esther; Minucci, Sergio; Politano, Luisa Journal: Molecular reproduction and development Issue: Volume 87:Issue 1(2020) Page Start: 45 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗