R. Ferrante

Neurochemical and histologic characterization of striatal excitotoxic lesions produced by the mitochondrial toxin 3-nitropropionic acid

B. Hyman, B. Rosen, M. Beal, 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

Proliferative and degenerative changes in striatal spiny neurons in Huntington's disease: a combined study using the section-Golgi method and calbindin D28k immunocytochemistry

N W Kowall, R J Ferrante, E P Richardson, 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

Huntington’s Disease: Neuropathological Grading

J. Vonsattel, R. Myers, E. Bird, 1987 .

Chronic quinolinic acid lesions in rats closely resemble Huntington's disease

M. Beal, N. Kowall, K. Swartz, 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

Blockade of neuronal nitric oxide synthase protects against excitotoxicity in vivo

P. Mecocci, B. Jenkins, D. Siwek, 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

Systemic approaches to modifying quinolinic acid striatal lesions in rats

M. Beal, N. Kowall, K. Swartz, 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

Mice lacking cytosolic copper/zinc superoxide dismutase display a distinctive motor axonopathy

J. Shefner, D. Flood, A. Reaume, 1999, Neurology.

Neuronal Plasticity: A Potential Role in Spiny Striatal Neuron Degeneration in Huntington's Disease

N. Kowall, E. Richardson, R. Ferrante, 1994 .