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Neurobiology of Aging|November 15, 2011
VCP mutations in familial and sporadic amyotrophic lateral sclerosisMax Koppers, Marka M van Blitterswijk, Lotte Vlam, et al.
Human Molecular Genetics|May 18, 2013
ALS-associated mutations in FUS disrupt the axonal distribution and function of SMNEwout J N Groen, Katsumi Fumoto, Anna M Blokhuis, et al.
The American Journal of Gastroenterology|March 22, 2017
Risk for Incomplete Resection after Macroscopic Radical Endoscopic Resection of T1 Colorectal Cancer: A Multicenter Cohort StudyY Backes, W H de Vos Tot Nederveen Cappel, J van Bergeijk, et al.
Genome Medicine|March 22, 2025
Long-read sequencing identifies copy-specific markers of SMN gene conversion in spinal muscular atrophyM M Zwartkruis, M G Elferink, D Gommers, et al.
Acta Neuropathologica Communications|September 17, 2024
Molecular pathology, developmental changes and synaptic dysfunction in (pre-) symptomatic human C9ORF72-ALS/FTD cerebral organoidsAstrid T van der Geest, Channa E Jakobs, Tijana Ljubikj, et al.
Plos One|April 18, 2012
Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALSFrank P Diekstra, Christiaan G J Saris, Wouter van Rheenen, et al.
Neurobiology of Aging|May 20, 2014
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival studyPerry T C van Doormaal, Nicola Ticozzi, Cinzia Gellera, et al.
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