Clostridial Cellulitis in the Horse: A Report of Five Cases

Por Valberg, S. J., McKinnon, A. O.
Publicado em 1984

Muscle glycogen concentrations and response to diet and exercise regimes in Warmblood horses with type 2 Polysaccharide Storage Myopathy

Por Williams, Zoë J., Bertels, Megan, Valberg, Stephanie J.
Publicado no PLoS One (2018)

Effects of feeding two RRR-α-tocopherol formulations on serum, cerebrospinal fluid and muscle α-tocopherol concentrations in horses with subclinical vitamin E deficiency

Por Brown, J. C., Valberg, S. J., Hogg, M., Finno, C. J.
Publicado no Equine Vet J (2017)

Clinical and histopathological features of myofibrillar myopathy in Warmblood horses

Por VALBERG, S. J., NICHOLSON, A. M., LEWIS, S. S., REARDON, R. A., FINNO, C. J.
Publicado no Equine Vet J (2017)

Proteome and transcriptome profiling of equine myofibrillar myopathy identifies diminished peroxiredoxin 6 and altered cysteine metabolic pathways

Por Valberg, Stephanie J., Perumbakkam, Sudeep, McKenzie, Erica C., Finno, Carrie J.
Publicado no Physiol Genomics (2018)

Haplotype diversity in the equine myostatin gene with focus on variants associated with race distance propensity and muscle fiber type proportions

Por Petersen, Jessica L, Valberg, Stephanie J, Mickelson, James R, McCue, Molly E
Publicado em 2014

Evidence of the Primary Afferent Tracts Undergoing Neurodegeneration in Horses With Equine Degenerative Myeloencephalopathy Based on Calretinin Immunohistochemical Localization

Por Finno, C. J., Valberg, S. J., Shivers, J., D’Almeida, E., Armién, A. G.
Publicado no Vet Pathol (2015)

Acquired multiple acyl-CoA dehydrogenase deficiency and marked selenium deficiency causing severe rhabdomyolysis in a horse

Por Gomez, Diego E., Valberg, Stephanie J., Magdesian, K. Gary, Hanna, Paul E., Lofstedt, Jeanne
Publicado no Can Vet J (2015)

An E321G MYH1 mutation is strongly associated with nonexertional rhabdomyolysis in Quarter Horses

Por Valberg, Stephanie J., Henry, Marisa L., Perumbakkam, Sudeep, Gardner, Keri L., Finno, Carrie J.
Publicado no J Vet Intern Med (2018)

Genetic mapping of recurrent exertional rhabdomyolysis in a population of North American Thoroughbreds

Por Fritz, K.L., McCue, M.E., Valberg, S.J., Rendahl, A.K., Mickelson, J.R.
Publicado em 2012

Concurrent Equine Degenerative Myeloencephalopathy and Equine Motor Neuron Disease in Three Young Horses

Por Finno, C.J., Miller, A.D., Sisó, S., Divers, T., Gianino, G., Barro, M.V., Valberg, S.J.
Publicado no J Vet Intern Med (2016)

Pigment retinopathy in warmblood horses with equine degenerative myeloencephalopathy and equine motor neuron disease

Por Finno, Carrie J., Kaese, Heather J., Miller, Andrew D., Gianino, Giuliana, Divers, Thomas, Valberg, Stephanie J.
Publicado no Vet Ophthalmol (2016)

Suspected myofibrillar myopathy in Arabian horses with a history of exertional rhabdomyolysis

Por VALBERG, S. J., McKENZIE, E. C., EYRICH, L. V., SHIVERS, J., BARNES, N. E., FINNO, C. J.
Publicado no Equine Vet J (2015)

Prevalence of the E321G MYH1 variant for immune‐mediated myositis and nonexertional rhabdomyolysis in performance subgroups of American Quarter Horses

Por Gianino, Giuliana M., Valberg, Stephanie J., Perumbakkam, Sudeep, Henry, Marisa L., Gardner, Keri, Penedo, Cecilia, Finno, Carrie J.
Publicado no J Vet Intern Med (2019)

Major Histocompatibility Complex I and II Expression and Lymphocytic Subtypes in Muscle of Horses with Immune‐Mediated Myositis

Por Durward‐Akhurst, S.A., Finno, C.J., Barnes, N., Shivers, J., Guo, L.T., Shelton, G.D., Valberg, S.J.
Publicado no J Vet Intern Med (2016)

Glycogen synthase (GYS1) mutation causes a novel skeletal muscle glycogenosis

Por McCue, Molly E, Valberg, Stephanie J, Miller, Michael B, Wade, Claire, DiMauro, Salvatore, Akman, Hasan O, Mickelson, James R
Publicado em 2008

Suspected Congenital Centronuclear Myopathy in an Arabian‐cross Foal

Por Polle, F., Andrews, F.M., Gillon, T., Eades, S.C., McConnico, R.S., Strain, G.M., Valberg, S.J., Guo, L.T., Shelton, G.D.
Publicado no J Vet Intern Med (2014)

Evidence of Positive Selection for a Glycogen Synthase (GYS1) Mutation in Domestic Horse Populations

Por McCoy, Annette M., Schaefer, Robert, Petersen, Jessica L., Morrell, Peter L., Slamka, Megan A., Mickelson, James R., Valberg, Stephanie J., McCue, Molly E.
Publicado em 2014

Transcriptome profiling of equine vitamin E deficient neuroaxonal dystrophy identifies upregulation of liver X receptor target genes

Por Finno, Carrie J., Bordbari, Matthew H., Valberg, Stephanie J., Lee, David, Herron, Josi, Hines, Kelly, Monsour, Tamer, Scott, Erica, Bannasch, Danika L., Mickelson, James, Xu, Libin
Publicado no Free Radic Biol Med (2016)

Identification of long non-coding RNA in the horse transcriptome

Por Scott, E. Y., Mansour, T., Bellone, R. R., Brown, C. T., Mienaltowski, M. J., Penedo, M. C., Ross, P. J., Valberg, S. J., Murray, J. D., Finno, C. J.
Publicado no BMC Genomics (2017)