Lindsey J. Miller

Deficits in stepping response time are associated with impairments in balance and mobility in people with Huntington disease

Allon Goldberg, S. Feely, C. Siskind, 2010, Journal of the Neurological Sciences.

Charcot‐marie‐tooth disease subtypes and genetic testing strategies

M. Shy, S. Feely, S. Sottile, 2011, Annals of neurology.

Mutations in the tail domain of DYNC1H1 cause dominant spinal muscular atrophy

A. Pestronk, R. Vallee, F. Muntoni, 2012, Neurology.

PMP22 expression in dermal nerve myelin from patients with CMT1A.

I. Katona, Xingyao Wu, M. Shy, 2009, Brain : a journal of neurology.

High-dosage ascorbic acid treatment in Charcot-Marie-Tooth disease type 1A: results of a randomized, double-masked, controlled trial.

R. Lewis, M. Mcdermott, D. Herrmann, 2013, JAMA neurology.

Strategy for genetic testing in Charcot-Marie-Disease

M. Shy, S. Feely, S. Sottile, 2011, Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology.

Anterior tibialis cmap amplitude correlations with impairment in CMT1A

M. Shy, S. Feely, C. Siskind, 2013, Muscle & nerve.