Steven U. Walkley, DVM
Affiliations: | Neurosciences | Albert Einstein College of Medicine, New York, New York, United States |
Area:
Lysosomal DisordersWebsite:
http://www.einstein.yu.edu/faculty/7668/steven-walkley/Google:
"Steven Walkley"Mean distance: 106866
Children
Sign in to add trainee| Mark Zervas | grad student | 2001 | Yeshiva University (Cell Biology Tree) |
| Marjorie C. Gondre-Lewis | grad student | 2003 | Yeshiva University (Anatomy Tree) |
| Cristin Davidson | grad student | 2013 | Yeshiva University |
| Matthew C. Micsenyi | grad student | 2013 | Yeshiva University |
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Walkley SU. (2021) Rethinking lysosomes and lysosomal disease. Neuroscience Letters. 762: 136155 |
| Davidson J, Molitor E, Moores S, et al. (2019) 2-Hydroxypropyl-β-cyclodextrin is the active component in a triple combination formulation for treatment of Niemann-Pick C1 disease. Biochimica Et Biophysica Acta. Molecular and Cell Biology of Lipids |
| Davidson C, Gibson A, Gu T, et al. (2019) Improved disease amelioration with combination therapy for Niemann-Pick disease type C1 Molecular Genetics and Metabolism. 126: S46 |
| Kerner-Rossi M, Gulinello M, Walkley S, et al. (2018) Pathobiology of Christianson syndrome: Linking disrupted endosomal-lysosomal function with intellectual disability and sensory impairments. Neurobiology of Learning and Memory. 165: 106867 |
| Boudewyn LC, Walkley SU. (2018) Current concepts in the neuropathogenesis of mucolipidosis type IV. Journal of Neurochemistry |
| Ory DS, Ottinger EA, Farhat NY, et al. (2017) Intrathecal 2-hydroxypropyl-β-cyclodextrin decreases neurological disease progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial. Lancet (London, England) |
| Boudewyn LC, Sikora J, Kuchar L, et al. (2017) N-butyl-deoxynojirimycin delays motor deficits, cerebellar microgliosis, and Purkinje cell loss in a mouse model of mucolipidosis type IV. Neurobiology of Disease |
| Sikora J, Dworski S, Jones EE, et al. (2017) Acid Ceramidase Deficiency in Mice Results in a Broad Range of Central Nervous System Abnormalities. The American Journal of Pathology. 187: 864-883 |
| Yang DS, Stavrides P, Kumar A, et al. (2017) Cyclodextrin has conflicting actions on autophagy flux in vivo in brains of normal and Alzheimer model mice. Human Molecular Genetics |
| Patterson MC, Walkley SU. (2016) Niemann-Pick disease, type C and Roscoe Brady. Molecular Genetics and Metabolism |