• 60 Citations
  • 3 h-Index
20142018
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Research Output 2014 2018

  • 60 Citations
  • 3 h-Index
  • 5 Article
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Article
2018
3 Citations (Scopus)

Arginase-1 expressing microglia in close proximity to motor neurons were increased early in disease progression in canine degenerative myelopathy, a model of amyotrophic lateral sclerosis

Toedebusch, C., Snyder, J. C., Jones, M. R., Garcia, V. B., Johnson, G. C., Villalón, E. L., Coates, J. R. & Garcia, M. L., Apr 1 2018, In : Molecular and Cellular Neuroscience. 88, p. 148-157 10 p.

Research output: Contribution to journalArticle

Arginase
Spinal Cord Diseases
Amyotrophic Lateral Sclerosis
Microglia
Motor Neurons
2017
2 Citations (Scopus)

Cerebrospinal Fluid Levels of Phosphorylated Neurofilament Heavy as a Diagnostic Marker of Canine Degenerative Myelopathy

Toedebusch, C., Bachrach, M. D., Garcia, V. B., Johnson, G. C., Katz, M. L., Shaw, G., Coates, J. R. & Garcia, M. L., Mar 1 2017, In : Journal of Veterinary Internal Medicine. 31, 2, p. 513-520 8 p.

Research output: Contribution to journalArticle

Intermediate Filaments
Spinal Cord Diseases
cerebrospinal fluid
Cerebrospinal Fluid
Canidae
1 Citation (Scopus)

Muscle spindle alterations precede onset of sensorimotor deficits in Charcot–Marie–Tooth type 2E

Villalón, E., Jones, M. R., Toedebusch, C., Zino, S. J., Dale, J. M., Landayan, D. S., Shen, H., Cornelison, D. D. W. & Garcia, M. L., Feb 1 2017, In : Genes, Brain and Behavior. 16, 2, p. 260-270 11 p.

Research output: Contribution to journalArticle

Muscle Spindles
Intermediate Filaments
Light
Pathology
Muscular Atrophy
2016
7 Citations (Scopus)

Rescue of a mouse model of spinal muscular atrophy with respiratory distress type 1 by AAV9-IGHMBP2 is dose dependent

Shababi, M., Feng, Z., Villalon, E., Toedebusch, C., Osman, E. Y., Miller, M. R., Williams-Simon, P. A., Lombardi, A., Sass, T. H., Atkinson, A. K., Garcia, M. L., Ko, C. P. & Lorson, C. L., May 1 2016, In : Molecular Therapy. 24, 5, p. 855-866 12 p.

Research output: Contribution to journalArticle

Motor Neurons
Genes
Injections
Muscular Atrophy
Viral Genes
2014
47 Citations (Scopus)

Enzyme replacement therapy attenuates disease progression in a canine model of late-infantile neuronal ceroid lipofuscinosis (CLN2 disease)

Katz, M. L., Coates, J. R., Toedebusch, C., Taylor, J. D., Carpentier, M., Young, W. M., Wininger, F. A., Kennedy, D., Vuillemenot, B. R. & O'Neill, C. A., Jan 1 2014, In : Journal of Neuroscience Research. 92, 11, p. 1591-1598 8 p.

Research output: Contribution to journalArticle

Neuronal Ceroid-Lipofuscinoses
Enzyme Replacement Therapy
Disease Progression
Canidae
Cerebrospinal Fluid