Costanza Lamperti

A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score

Gabriele Siciliano, Lucio Santoro, Leda Volpi, 2010, Muscle & nerve.

Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies

Daniele Ghezzi, Massimo Zeviani, Cristina Smiderle, 2011, Nature Genetics.

Distinctive patterns of microRNA expression in primary muscular disorders

Isaac S. Kohane, Alan H. Beggs, Alal Eran, 2007, Proceedings of the National Academy of Sciences.

Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up

Anna Carla Turconi, Domenico Coviello, N. Bresolin, 2011, Journal of Neurology.