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Heather G Stewart

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Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 24, 2006
Corticomotoneuronal dysfunction in ALS patients with different SOD1 mutationsHeather G Stewart, Peter M Andersen, Andrew Eisen, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|April 23, 2008
SOD1 gene mutations in ALS patients from British Columbia, Canada: clinical features, neurophysiology and ethical issues in managementAndrew Eisen, Michelle M Mezei, Heather G Stewart, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 24, 2007
Soluble misfolded subfractions of mutant superoxide dismutase-1s are enriched in spinal cords throughout life in murine ALS modelsPer Zetterström, Heather G Stewart, Daniel Bergemalm, et al.
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Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 24, 2006
Corticomotoneuronal dysfunction in ALS patients with different SOD1 mutationsHeather G Stewart, Peter M Andersen, Andrew Eisen, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|April 23, 2008
SOD1 gene mutations in ALS patients from British Columbia, Canada: clinical features, neurophysiology and ethical issues in managementAndrew Eisen, Michelle M Mezei, Heather G Stewart, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 24, 2007
Soluble misfolded subfractions of mutant superoxide dismutase-1s are enriched in spinal cords throughout life in murine ALS modelsPer Zetterström, Heather G Stewart, Daniel Bergemalm, et al.
Pageof 1