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Parkinsonism & Related Disorders|November 5, 2018
New Era in disease modification in Parkinson's disease: Review of genetically targeted therapeuticsS Pablo Sardi, Tanya Simuni
Movement Disorders : Official Journal of the Movement Disorder Society|April 29, 2018
Targeted Therapies for Parkinson's Disease: From Genetics to the ClinicS Pablo Sardi, Jesse M Cedarbaum, Patrik Brundin
Progress in Neurobiology|January 10, 2015
Gaucher-related synucleinopathies: the examination of sporadic neurodegeneration from a rare (disease) angleS Pablo Sardi, Seng H Cheng, Lamya S Shihabuddin
Scientific Reports|January 13, 2021
Sterol auto-oxidation adversely affects human motor neuron viability and is a neuropathological feature of amyotrophic lateral sclerosisJames C Dodge, Jinlong Yu, S Pablo Sardi, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 24, 2006
Notch1 signaling regulates radial glia differentiation through multiple transcriptional mechanismsBrooke A Patten, S Pablo Sardi, Samir Koirala, et al.
Cell|October 5, 2006
Presenilin-dependent ErbB4 nuclear signaling regulates the timing of astrogenesis in the developing brainS Pablo Sardi, Joshua Murtie, Samir Koirala, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 2, 2018
New Frontiers in Parkinson's Disease: From Genetics to the ClinicLamya S Shihabuddin, Patrik Brundin, J Timothy Greenamyre, et al.
Neuro-Degenerative Diseases|February 14, 2012
Mutant GBA1 expression and synucleinopathy risk: first insights from cellular and mouse modelsS Pablo Sardi, Priyanka Singh, Seng H Cheng, et al.
Genes & Development|July 18, 2018
Dysregulation of Mdm2 and Mdm4 alternative splicing underlies motor neuron death in spinal muscular atrophyMeaghan Van Alstyne, Christian M Simon, S Pablo Sardi, et al.
Neurobiology of Disease|June 25, 2019
Viral delivery of a microRNA to Gba to the mouse central nervous system models neuronopathic Gaucher diseaseKasey L Jackson, Catherine Viel, Jennifer Clarke, et al.
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