Mary B. Davis

Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort

M. Roberts, F. Muntoni, R. Horvath, 2012, Journal of Neurology.

Autosomal-dominant GTPCH1-deficient DRD: clinical characteristics and long-term outcome of 34 patients

K. Bhatia, M. Sweeney, J. Polke, 2009, Journal of Neurology Neurosurgery & Psychiatry.

Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype

R. Griggs, M. Davis, M. Hanna, 2011, Neurology.

Variable phenotypes are associated with PMP22 missense mutations

David L. Bennett, M. Russo, M. Laurá, 2011, Neuromuscular Disorders.