D. Moore

PolyQ Tract Toxicity in SCA1 is Length Dependent in the Absence of CAG Repeat Interruption

M. Sweeney, P. Giunti, Mary B. Davis, 2018, Front. Cell. Neurosci..

Leber Hereditary Optic Neuropathy and Longitudinally Extensive Transverse Myelitis.

G. Gole, D. Mackey, L. Kearns, 2018, JIMD reports.

Detection of novel mutations and review of published data suggests that hereditary spastic paraplegia caused by spastin (SPAST) mutations is found more often in males

N. Wood, H. Houlden, C. Proukakis, 2011, Journal of the Neurological Sciences.

Evidence for neuroaxonal injury in patients with proteolipid protein gene mutations

R. Schiffmann, G. Tedeschi, S. Bonavita, 2001, Neurology.