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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|January 20, 2017
A risk stratifying tool to facilitate safe late-stage percutaneous endoscopic gastrostomy in ALSAlexander G Thompson, Victoria Blackwell, Rachael Marsden, et al.Human Molecular Genetics|June 7, 2020
Correction of amyotrophic lateral sclerosis related phenotypes in induced pluripotent stem cell-derived motor neurons carrying a hexanucleotide expansion mutation in C9orf72 by CRISPR/Cas9 genome editing using homology-directed repairNidaa A Ababneh, Jakub Scaber, Rowan Flynn, et al.Clinical Proteomics|August 22, 2020
CSF extracellular vesicle proteomics demonstrates altered protein homeostasis in amyotrophic lateral sclerosisAlexander G Thompson, Elizabeth Gray, Imre Mäger, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 24, 2020
The use of biotelemetry to explore disease progression markers in amyotrophic lateral sclerosisMadeline Kelly, Arseniy Lavrov, Luis Garcia-Gancedo, et al.Biochimica Et Biophysica Acta|June 13, 2006
The molecular genetics of non-ALS motor neuron diseasesPaul A James, Kevin TalbotProgress in Neurobiology|February 20, 2008
Transgenics, toxicity and therapeutics in rodent models of mutant SOD1-mediated familial ALSBradley J Turner, Kevin TalbotAnnals of Neurology|January 14, 2018
Cerebrospinal fluid macrophage biomarkers in amyotrophic lateral sclerosisAlexander G Thompson, Elizabeth Gray, Marie-Laëtitia Thézénas, et al.Acta Neuropathologica Communications|July 4, 2020
Quantitative patterns of motor cortex proteinopathy across ALS genotypesMatthew Nolan, Connor Scott, Menuka Pallebage Gamarallage, et al.JMIR Mhealth and Uhealth|December 21, 2019
Objectively Monitoring Amyotrophic Lateral Sclerosis Patient Symptoms During Clinical Trials With Sensors: Observational StudyLuis Garcia-Gancedo, Madeline L Kelly, Arseniy Lavrov, et al.Pageof 35