N. Russo

The epsilon-sarcoglycan gene in myoclonic syndromes

Hee Taek Kim, M. Edwards, N. Quinn, 2005, Neurology.

Agrypnia excitata in a patient with progeroid short stature and pigmented Nevi (Mulvihill‐Smith syndrome)

P. Bosco, R. Ferri, B. Lanuzza, 2005, Journal of sleep research.

Hereditary haemochromatosis is unlikely to cause movement disorders

M. Edwards, K. Bhatia, T. Andrews, 2004, Journal of Neurology.