Julia D. Hicks

Increased frequency of congenital heart defects in Menkes disease

T. Pierson, S. Kaler, A. Donsante, 2012, Clinical dysmorphology.

Molecular and biochemical characterization of a unique mutation in CCS, the human copper chaperone to superoxide dismutase

P. Huppke, P. J. Steinbach, S. Kaler, 2012, Human mutation.

Molecular correlates of epilepsy in early diagnosed and treated Menkes disease

S. Kaler, Susumu Sato, A. Donsante, 2010, Journal of Inherited Metabolic Disease.