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Orphanet Journal of Rare Diseases|November 27, 2014
Cryptogenic stroke and small fiber neuropathy of unknown etiology in patients with alpha-galactosidase A -10T genotypeMichael Schelleckes, Malte Lenders, Katrin Guske, et al.
Cell Death & Disease|August 12, 2022
Acidosis induces RIPK1-dependent death of glioblastoma stem cells via acid-sensing ion channel 1aJan Clusmann, Klaus-Daniel Cortés Franco, David Alejandro Corredor Suárez, et al.
The Journal of Gene Medicine|February 20, 2025
RNA Interference Targeting Small Heat Shock Protein B8 Failed to Improve Distal Hereditary Motor Neuropathy in the Mouse ModelLeen Vendredy, Vicky De Winter, Jonas Van Lent, et al.
Archives of Neurology|June 15, 2011
Neuropathy in a human without the PMP22 geneMario Andre Saporta, Istvan Katona, Xuebao Zhang, et al.
Nature Communications|September 27, 2012
Uncoupling of the endocannabinoid signalling complex in a mouse model of fragile X syndromeKwang-Mook Jung, Marja Sepers, Christopher M Henstridge, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 16, 2019
Myelinating Glia-Specific Deletion of Fbxo7 in Mice Triggers Axonal Degeneration in the Central Nervous System Together with Peripheral NeuropathySabitha Joseph, Siv Vingill, Olaf Jahn, et al.
Journal of Alzheimer'S Disease : JAD|April 7, 2020
Aggregates of RNA Binding Proteins and ER Chaperones Linked to Exosomes in Granulovacuolar Degeneration of the Alzheimer's Disease BrainAlfred Yamoah, Priyanka Tripathi, Antonio Sechi, et al.
Nature Communications|December 10, 2015
Cold-aggravated pain in humans caused by a hyperactive NaV1.9 channel mutantEnrico Leipold, Andrea Hanson-Kahn, Miya Frick, et al.
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