M. Melis

Progressive apraxia of speech in a patient with a C9orf72 mutation

F. Marrosu, A. Cannas, S. Tranquilli, 2016, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Creutzfeldt-Jakob disease associated with high titer of antithyroid autoantibodies: case report and literature review

G. Cossu, A. Spissu, L. Pinna, 2003, Neurological Sciences.

Neurological phenomenology of the IRF2BPL mutation syndrome: Analysis of a new case and systematic review of the literature

L. Rocchi, G. Defazio, S. Giglio, 2022, Seizure.

Anti-Hu antibodies, sensory neuropathy, and Holmes–Adie syndrome in a patient with seminoma

G. Cossu, A. Spissu, A. Antonini, 2004 .

Bipolar affective disorder and Parkinson's disease: a rare, insidious and often unrecognized association

M. Giagheddu, P. Tacconi, A. Tuveri, 2002, Neurological Sciences.

[123I]FP-CIT SPECT findings in two patients with Hallervorden–Spatz disease with homozygous mutation in PANK2 gene

G. Cossu, A. Spissu, A. Antonini, 2005, Neurology.

Pathological gambling, delusional parasitosis and adipsia as a post-haemorrhagic syndrome: A case report

A. Cannas, P. Solla, M. Marrosu, 2008, Neurocase.