Steven U. Walkley, DVM

Neurosciences Albert Einstein College of Medicine, New York, New York, United States 
Lysosomal Disorders
"Steven Walkley"
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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
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Huizing M, Hackbarth ME, Adams DR, et al. (2021) Mini-Review Free Sialic Acid Storage Disorder: Progress and Promise. Neuroscience Letters. 135896
Walkley SU, Abbeduto L, Batshaw ML, et al. (2019) Intellectual and Developmental Disabilities Research Centers: 50 Years of Scientific Accomplishments. Annals of Neurology
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
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
Walkley SU, Davidson CD, Jacoby J, et al. (2016) Fostering collaborative research for rare genetic disease: the example of niemann-pick type C disease. Orphanet Journal of Rare Diseases. 11: 161
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