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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 21, 2021
Cardiac troponin T is elevated and increases longitudinally in ALS patientsUlf Kläppe, Sanharib Chamoun, Qing Shen, et al.Cerebellum & Ataxias|July 27, 2019
The cerebellar phenotype of Charcot-Marie-Tooth neuropathy type 4CHumberto Skott, Cristina Muntean-Firanescu, Kristin Samuelsson, et al.Journal of Pharmaceutical Sciences|October 30, 2020
Primary Human Hepatocyte Spheroid Model as a 3D In Vitro Platform for Metabolism StudiesKajsa P Kanebratt, Annika Janefeldt, Liisa Vilén, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 10, 2018
The Swedish motor neuron disease quality registryElisa Longinetti, Amanda Regodón Wallin, Kristin Samuelsson, et al.European Journal of Neurology|January 28, 2026
Novel Clinical Insights From a Swedish RFC1 Spectrum Disorder CohortVictor Alm, Linda Säll, Kristin Samuelsson, et al.Neurology. Genetics|March 18, 2021
Novel Mutation m.10372A>G in <i>MT-ND3</i> Causing Sensorimotor Axonal PolyneuropathyHelene Bruhn, Kristin Samuelsson, Florian A Schober, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 4, 2023
Neurodegenerative biomarkers outperform neuroinflammatory biomarkers in amyotrophic lateral sclerosisUlf Kläppe, Stefan Sennfält, Anikó Lovik, et al.Pharmacology Research & Perspectives|October 14, 2024
Disposition of orally administered atuliflapon, a novel 5-lipoxygenase-activating protein inhibitor in healthy participantsXue-Qing Li, Bo Lindmark, Carl Amilon, et al.Brain Communications|May 19, 2025
Plasma troponin T reflects lower motor neuron involvement on electromyography in amyotrophic lateral sclerosisSanharib Chamoun, Sofia Imrell, Zane Upate, et al.Muscle & Nerve|September 25, 2018
Screening for Fabry disease and Hereditary ATTR amyloidosis in idiopathic small-fiber and mixed neuropathyKristin Samuelsson, Ana Radovic, Rayomand Press, et al.Pageof 5