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Neurobiology of Aging|December 21, 2019
SQSTM1/p62 variants in 486 patients with familial ALS from Germany and SwedenRüstem Yilmaz, Kathrin Müller, David Brenner, et al.
Alcoholism, Clinical and Experimental Research|April 25, 2003
Hepatitis C and alcohol: fundamental and translational research directionsTimothy R Morgan, David Brenner, James Everhart, et al.
Neurogenetics|June 21, 2023
PSEN1/SLC20A2 double mutation causes early-onset Alzheimer's disease and primary familial brain calcification co-morbiditySophie Hebestreit, Janine Schwahn, Vesile Sandikci, et al.
Experimental Neurology|October 10, 2020
Hemizygous deletion of Tbk1 worsens neuromuscular junction pathology in TDP-43G298S transgenic miceKirsten Sieverding, Johannes Ulmer, Clara Bruno, et al.
Cell Death & Disease|August 3, 2024
Heterozygous knockout of Synaptotagmin13 phenocopies ALS features and TP53 activation in human motor neuronsJohannes Lehmann, Amr Aly, Christina Steffke, et al.
Neurobiology of Aging|May 10, 2022
Methylome analysis of ALS patients and presymptomatic mutation carriers in blood cellsWolfgang P Ruf, Eilis Hannon, Axel Freischmidt, et al.
Acta Neuropathologica|October 7, 2014
Inflammatory dysregulation of blood monocytes in Parkinson's disease patientsVeselin Grozdanov, Corinna Bliederhaeuser, Wolfgang P Ruf, et al.
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