Showing results 1 to 8 of 8
Title | Author(s) | Issue Date | |
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Burden of rare variants in ALS genes influences survival in familial and sporadic ALS Journal:Neurobiology of Aging | 2017 | ||
The default mode network is disrupted in Parkinson’s disease with visual hallucinations Journal:Human Brain Mapping | 2014 | ||
Deviation from baseline mutation burden provides powerful and robust rare-variants association test for complex diseases Journal:Nucleic Acids Research | 2022 | ||
Multimodal MRI of the hippocampus in Parkinson's disease with visual hallucinations Journal:Brain Structure and Function | 2014 | ||
PMCA4 (ATP2B4) Mutation in Familial Spastic Paraplegia Journal:PLoS ONE | 2014 | ||
PMCA4 (ATP2B4) mutation in familial spastic paraplegia causes delay in intracellular calcium extrusion Journal:Brain and Behavior | 2015 | ||
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