Showing results (161-170 of 176) with videos related to
Sort By:
Pageof 18
Neurology(R) Neuroimmunology & Neuroinflammation|June 25, 2025
Neuropathic Pain and Distinct CASPR2 Autoantibody IgG Subclasses Drive Neuronal HyperexcitabilityMargarita Habib, Anna-Lena Wiessler, Patrik Fischer, et al.Cell|September 22, 2009
Synaptic PRG-1 modulates excitatory transmission via lipid phosphate-mediated signalingThorsten Trimbuch, Prateep Beed, Johannes Vogt, et al.Scientific Reports|April 13, 2019
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosisAnnelot M Dekker, Frank P Diekstra, Sara L Pulit, et al.Brain : a Journal of Neurology|October 9, 2010
Loss of striatal type 1 cannabinoid receptors is a key pathogenic factor in Huntington's diseaseCristina Blázquez, Anna Chiarlone, Onintza Sagredo, et al.Journal of Neurology, Neurosurgery, and Psychiatry|April 14, 2018
Comprehensive analysis of the mutation spectrum in 301 German ALS familiesKathrin Müller, David Brenner, Patrick Weydt, et al.Neuron|September 28, 2011
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTDAlan E Renton, Elisa Majounie, Adrian Waite, et al.Brain : a Journal of Neurology|April 19, 2007
Large-scale pathways-based association study in amyotrophic lateral sclerosisDalia Kasperaviciute, Mike E Weale, Kevin V Shianna, et al.Nature Genetics|July 26, 2016
NEK1 variants confer susceptibility to amyotrophic lateral sclerosisKevin P Kenna, Perry T C van Doormaal, Annelot M Dekker, et al.Brain : a Journal of Neurology|January 18, 2018
Hot-spot KIF5A mutations cause familial ALSDavid Brenner, Rüstem Yilmaz, Kathrin Müller, et al.Developmental Cell|March 20, 2018
Opposing Effects of CREBBP Mutations Govern the Phenotype of Rubinstein-Taybi Syndrome and Adult SHH MedulloblastomaDaniel J Merk, Jasmin Ohli, Natalie D Merk, et al.Pageof 18