Stewart HG - Search Results

1

SOD1 gene mutations in ALS patients from British Columbia, Canada: clinical features, neurophysiology and ethical issues in management.

Eisen A, Mezei MM, Stewart HG, Fabros M, Gibson G, Andersen PM. Eisen A, et al. Among authors: stewart hg. Amyotroph Lateral Scler. 2008 Apr;9(2):108-19. doi: 10.1080/17482960801900073. Amyotroph Lateral Scler. 2008. PMID: 18428003

2

Corticomotoneuronal dysfunction in ALS patients with different SOD1 mutations.

Stewart HG, Andersen PM, Eisen A, Weber M. Stewart HG, et al. Clin Neurophysiol. 2006 Aug;117(8):1850-61. doi: 10.1016/j.clinph.2006.04.004. Epub 2006 Jun 21. Clin Neurophysiol. 2006. PMID: 16793335

3

Corticomotoneuronal connections in primary lateral sclerosis (PLS).

Weber M, Stewart H, Hirota N, Eisen A. Weber M, et al. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002 Dec;3(4):190-8. doi: 10.1080/146608202760839004. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002. PMID: 12710508

4

Preserved slow conducting corticomotoneuronal projections in amyotrophic lateral sclerosis with autosomal recessive D90A CuZn-superoxide dismutase mutation.

Weber M, Eisen A, Stewart HG, Andersen PM. Weber M, et al. Among authors: stewart hg. Brain. 2000 Jul;123 ( Pt 7):1505-15. doi: 10.1093/brain/123.7.1505. Brain. 2000. PMID: 10869061 Clinical Trial.

5

The physiological basis of conduction slowing in ALS patients homozygous for the D90A CuZn-SOD mutation.

Weber M, Eisen A, Stewart HG, Andersen PM, Hirota N. Weber M, et al. Among authors: stewart hg. Muscle Nerve. 2001 Jan;24(1):89-97. doi: 10.1002/1097-4598(200101)24:1<89::aid-mus10>3.0.co;2-i. Muscle Nerve. 2001. PMID: 11150970 Clinical Trial.

6

Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.

Mackenzie IR, Bigio EH, Ince PG, Geser F, Neumann M, Cairns NJ, Kwong LK, Forman MS, Ravits J, Stewart H, Eisen A, McClusky L, Kretzschmar HA, Monoranu CM, Highley JR, Kirby J, Siddique T, Shaw PJ, Lee VM, Trojanowski JQ. Mackenzie IR, et al. Ann Neurol. 2007 May;61(5):427-34. doi: 10.1002/ana.21147. Ann Neurol. 2007. PMID: 17469116

7

Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p.

Stewart H, Rutherford NJ, Briemberg H, Krieger C, Cashman N, Fabros M, Baker M, Fok A, DeJesus-Hernandez M, Eisen A, Rademakers R, Mackenzie IR. Stewart H, et al. Acta Neuropathol. 2012 Mar;123(3):409-17. doi: 10.1007/s00401-011-0937-5. Epub 2012 Jan 7. Acta Neuropathol. 2012. PMID: 22228244 Free PMC article.

8

Clinicopathological phenotype of ALS with a novel G72C SOD1 gene mutation mimicking a myopathy.

Stewart HG, Mackenzie IR, Eisen A, Brännström T, Marklund SL, Andersen PM. Stewart HG, et al. Muscle Nerve. 2006 May;33(5):701-6. doi: 10.1002/mus.20495. Muscle Nerve. 2006. PMID: 16435343

9

Cortical projections to spinal motoneurons: changes with aging and amyotrophic lateral sclerosis.

Eisen A, Entezari-Taher M, Stewart H. Eisen A, et al. Neurology. 1996 May;46(5):1396-404. doi: 10.1212/wnl.46.5.1396. Neurology. 1996. PMID: 8628489

10

Motor system abnormalities in heterozygous relatives of a D90A homozygous CuZn-SOD ALS patient of finnish extraction.

Mezei M, Andersen PM, Stewart H, Weber M, Eisen A. Mezei M, et al. J Neurol Sci. 1999 Oct 31;169(1-2):49-55. doi: 10.1016/s0022-510x(99)00215-4. J Neurol Sci. 1999. PMID: 10540007

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