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Brain Communications|October 28, 2021
SCFD1 expression quantitative trait loci in amyotrophic lateral sclerosis are differentially expressedAlfredo Iacoangeli, Isabella Fogh, Sashika Selvackadunco, et al.
Neurobiology of Aging|April 23, 2010
Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosisElke Bogaert, An Goris, Philip Van Damme, et al.
Muscle & Nerve|April 26, 2017
Finger extension weakness and downbeat nystagmus motor neuron disease syndrome: A novel motor neuron disorder?Aline Delva, Nimish Thakore, Erik P Pioro, et al.
Frontiers in Cellular Neuroscience|March 11, 2024
TUBA4A downregulation as observed in ALS post-mortem motor cortex causes ALS-related abnormalities in zebrafishEvelien Van Schoor, Dufie Strubbe, Elke Braems, et al.
The Lancet. Oncology|October 12, 2010
Treatment-related peripheral neuropathy in multiple myeloma: the challenge continuesMichel Delforge, Joan Bladé, Meletios A Dimopoulos, et al.
European Journal of Neurology|March 7, 2022
Respiratory onset of amyotrophic lateral sclerosis in a pregnant woman with a novel SOD1 mutationPegah Masrori, Simona Ospitalieri, Karin Forsberg, et al.
Stem Cell Reports|December 28, 2013
APP processing in human pluripotent stem cell-derived neurons is resistant to NSAID-based γ-secretase modulationJerome Mertens, Kathrin Stüber, Patrick Wunderlich, et al.
European Journal of Neurology|September 1, 2021
RNF170 mutation causes autosomal dominant sensory ataxia with variable pyramidal involvementSien H Van Daele, Matthieu Moisse, Valérie Race, et al.
Molecular Neurobiology|March 23, 2022
HDAC3 Inhibition Stimulates Myelination in a CMT1A Mouse ModelRobert Prior, Stijn Verschoren, Katlijn Vints, et al.
Neurobiology of Aging|September 23, 2017
NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patientsHung Phuoc Nguyen, Sara Van Mossevelde, Lubina Dillen, et al.
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