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Andreas Hermann

Showing results (311-320 of 348) with videos related to

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JAMA Neurology|January 10, 2022
Safety and Effectiveness of Long-term Intravenous Administration of Edaravone for Treatment of Patients With Amyotrophic Lateral SclerosisSimon Witzel, André Maier, Robert Steinbach, et al.
Human Molecular Genetics|January 10, 2018
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiencySarah J Brockmann, Axel Freischmidt, Patrick Oeckl, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|February 23, 2017
Eighth International Chorea-Acanthocytosis Symposium: Summary of Workshop Discussion and Action PointsSamuel S Pappas, Juan Bonifacino, Adrian Danek, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|April 16, 2021
Reconditioning the Neurogenic Niche of Adult Non-human Primates by Antisense Oligonucleotide-Mediated Attenuation of TGFβ SignalingSebastian Peters, Sabrina Kuespert, Eva Wirkert, et al.
European Journal of Neurology|January 19, 2024
In-depth analysis of data from the RAS-ALS study reveals new insights in rasagiline treatment for amyotrophic lateral sclerosisJoachim Schuster, Jens Dreyhaupt, Karla Mönkemöller, et al.
Brain : a Journal of Neurology|April 19, 2021
A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosisAxel Freischmidt, Anand Goswami, Katharina Limm, et al.
Annals of Clinical and Translational Neurology|May 4, 2026
Impact of Plasma p-tau181 on Cognition, Motor Phenotypes, and Disease Course in ALSElisabeth Kasper, Annaliis Lehto, Nina Nordmann, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 9, 2025
"The DESCRIBE-ALS-FTD study: a prospective multicenter observational study of the ALS-FTD spectrum"Andreas Hermann, Johannes Prudlo, Elisabeth Kasper, et al.
Acta Neuropathologica Communications|April 24, 2025
Premature skeletal muscle aging in VPS13A deficiency relates to impaired autophagyVeronica Riccardi, Carlo Fiore Viscomi, Marco Sandri, et al.
Human Molecular Genetics|November 26, 2013
Human iPSC models of neuronal ceroid lipofuscinosis capture distinct effects of TPP1 and CLN3 mutations on the endocytic pathwayXenia Lojewski, John F Staropoli, Sunita Biswas-Legrand, et al.
Pageof 35

Showing results (311-320 of 348) with videos related to

Sort By:
Pageof 35
JAMA Neurology|January 10, 2022
Safety and Effectiveness of Long-term Intravenous Administration of Edaravone for Treatment of Patients With Amyotrophic Lateral SclerosisSimon Witzel, André Maier, Robert Steinbach, et al.
Human Molecular Genetics|January 10, 2018
CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiencySarah J Brockmann, Axel Freischmidt, Patrick Oeckl, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|February 23, 2017
Eighth International Chorea-Acanthocytosis Symposium: Summary of Workshop Discussion and Action PointsSamuel S Pappas, Juan Bonifacino, Adrian Danek, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|April 16, 2021
Reconditioning the Neurogenic Niche of Adult Non-human Primates by Antisense Oligonucleotide-Mediated Attenuation of TGFβ SignalingSebastian Peters, Sabrina Kuespert, Eva Wirkert, et al.
European Journal of Neurology|January 19, 2024
In-depth analysis of data from the RAS-ALS study reveals new insights in rasagiline treatment for amyotrophic lateral sclerosisJoachim Schuster, Jens Dreyhaupt, Karla Mönkemöller, et al.
Brain : a Journal of Neurology|April 19, 2021
A serum microRNA sequence reveals fragile X protein pathology in amyotrophic lateral sclerosisAxel Freischmidt, Anand Goswami, Katharina Limm, et al.
Annals of Clinical and Translational Neurology|May 4, 2026
Impact of Plasma p-tau181 on Cognition, Motor Phenotypes, and Disease Course in ALSElisabeth Kasper, Annaliis Lehto, Nina Nordmann, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|June 9, 2025
"The DESCRIBE-ALS-FTD study: a prospective multicenter observational study of the ALS-FTD spectrum"Andreas Hermann, Johannes Prudlo, Elisabeth Kasper, et al.
Acta Neuropathologica Communications|April 24, 2025
Premature skeletal muscle aging in VPS13A deficiency relates to impaired autophagyVeronica Riccardi, Carlo Fiore Viscomi, Marco Sandri, et al.
Human Molecular Genetics|November 26, 2013
Human iPSC models of neuronal ceroid lipofuscinosis capture distinct effects of TPP1 and CLN3 mutations on the endocytic pathwayXenia Lojewski, John F Staropoli, Sunita Biswas-Legrand, et al.
Pageof 35