Published in Neurology on January 30, 2007
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron (2011) 18.73
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Temporal trends in pre-surgical evaluations and epilepsy surgery in the U.S. from 1998 to 2009. Epilepsy Res (2012) 1.00
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A transcription factor map as revealed by a genome-wide gene expression analysis of whole-blood mRNA transcriptome in multiple sclerosis. PLoS One (2010) 1.00
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Deep brain stimulation for movement disorders. Neurotherapeutics (2014) 0.89
Late onset Alzheimer's disease in older people. Clin Interv Aging (2010) 0.89
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Expanding the genetics of amyotrophic lateral sclerosis and frontotemporal dementia. Alzheimers Res Ther (2012) 0.87
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Vitamin D(3) at 50x AI attenuates the decline in paw grip endurance, but not disease outcomes, in the G93A mouse model of ALS, and is toxic in females. PLoS One (2013) 0.85
Harnessing the power of metabolism for seizure prevention: focus on dietary treatments. Epilepsy Behav (2012) 0.85
The role of high-frequency oscillations in epilepsy surgery planning. Cochrane Database Syst Rev (2014) 0.84
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Electrode localization for planning surgical resection of the epileptogenic zone in pediatric epilepsy. Int J Comput Assist Radiol Surg (2013) 0.84
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Exploring new pathways of neurodegeneration in ALS: the role of mitochondria quality control. Brain Res (2014) 0.84
Caenorhabditis elegans: a model to investigate oxidative stress and metal dyshomeostasis in Parkinson's disease. Front Aging Neurosci (2014) 0.84
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Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein. Nat Genet (2000) 6.12
The role of radiotracer imaging in Parkinson disease. Neurology (2005) 3.02
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A chromosome 4p haplotype segregating with Parkinson's disease and postural tremor. Hum Mol Genet (1999) 1.43
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