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Paul Lingor

Showing results (131-140 of 173) with videos related to

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Cell Death and Differentiation|April 29, 2020
Inhibition of the autophagic protein ULK1 attenuates axonal degeneration in vitro and in vivo, enhances translation, and modulates splicingBjörn Friedhelm Vahsen, Vinicius Toledo Ribas, Jonas Sundermeyer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 1, 2022
Bi-Allelic COQ4 Variants Cause Adult-Onset Ataxia-Spasticity Spectrum DiseaseIsabell Cordts, Luisa Semmler, Jannik Prasuhn, et al.
Gigascience|December 18, 2024
A dataset profiling the multiomic landscape of the prefrontal cortex in amyotrophic lateral sclerosisFabian Hausmann, Lucas Caldi Gomes, Sonja Hänzelmann, et al.
Neurological Research and Practice|April 27, 2025
Motor phenotypes of amyotrophic lateral sclerosis - a three-determinant anatomical classification based on the region of onset, propagation of motor symptoms, and the degree of upper and lower motor neuron dysfunctionThomas Meyer, Matthias Boentert, Julian Großkreutz, et al.
Neurology|February 13, 2025
Long-Term Dynamics of CSF and Serum Neurofilament Light Chain in Adult Patients With 5q Spinal Muscular Atrophy Treated With NusinersenIsabell Cordts, Cornelia Fuetterer, Annika Wachinger, et al.
Human Molecular Genetics|September 17, 2011
The spinal muscular atrophy disease protein SMN is linked to the Rho-kinase pathway via profilinAnna Nölle, Andre Zeug, Jeroen van Bergeijk, et al.
Emerging Infectious Diseases|February 23, 2022
Infection Control Measures and Prevalence of SARS-CoV-2 IgG among 4,554 University Hospital Employees, Munich, GermanyJohanna Erber, Verena Kappler, Bernhard Haller, et al.
Journal of Neurochemistry|April 1, 2006
Granulocyte-colony stimulating factor is neuroprotective in a model of Parkinson's diseaseKatrin Meuer, Claudia Pitzer, Peter Teismann, et al.
Annals of Clinical and Translational Neurology|February 22, 2022
Validity and reliability of the German multidimensional fatigue inventory in spinal muscular atrophyCamilla Binz, Alma Osmanovic, Nele H Thomas, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 17, 2026
ALS motor phenotypes: a revised 'OPM' classificationThomas Meyer, Nicola Ticozzi, Markus Weber, et al.
Pageof 18

Showing results (131-140 of 173) with videos related to

Sort By:
Pageof 18
Cell Death and Differentiation|April 29, 2020
Inhibition of the autophagic protein ULK1 attenuates axonal degeneration in vitro and in vivo, enhances translation, and modulates splicingBjörn Friedhelm Vahsen, Vinicius Toledo Ribas, Jonas Sundermeyer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 1, 2022
Bi-Allelic COQ4 Variants Cause Adult-Onset Ataxia-Spasticity Spectrum DiseaseIsabell Cordts, Luisa Semmler, Jannik Prasuhn, et al.
Gigascience|December 18, 2024
A dataset profiling the multiomic landscape of the prefrontal cortex in amyotrophic lateral sclerosisFabian Hausmann, Lucas Caldi Gomes, Sonja Hänzelmann, et al.
Neurological Research and Practice|April 27, 2025
Motor phenotypes of amyotrophic lateral sclerosis - a three-determinant anatomical classification based on the region of onset, propagation of motor symptoms, and the degree of upper and lower motor neuron dysfunctionThomas Meyer, Matthias Boentert, Julian Großkreutz, et al.
Neurology|February 13, 2025
Long-Term Dynamics of CSF and Serum Neurofilament Light Chain in Adult Patients With 5q Spinal Muscular Atrophy Treated With NusinersenIsabell Cordts, Cornelia Fuetterer, Annika Wachinger, et al.
Human Molecular Genetics|September 17, 2011
The spinal muscular atrophy disease protein SMN is linked to the Rho-kinase pathway via profilinAnna Nölle, Andre Zeug, Jeroen van Bergeijk, et al.
Emerging Infectious Diseases|February 23, 2022
Infection Control Measures and Prevalence of SARS-CoV-2 IgG among 4,554 University Hospital Employees, Munich, GermanyJohanna Erber, Verena Kappler, Bernhard Haller, et al.
Journal of Neurochemistry|April 1, 2006
Granulocyte-colony stimulating factor is neuroprotective in a model of Parkinson's diseaseKatrin Meuer, Claudia Pitzer, Peter Teismann, et al.
Annals of Clinical and Translational Neurology|February 22, 2022
Validity and reliability of the German multidimensional fatigue inventory in spinal muscular atrophyCamilla Binz, Alma Osmanovic, Nele H Thomas, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|March 17, 2026
ALS motor phenotypes: a revised 'OPM' classificationThomas Meyer, Nicola Ticozzi, Markus Weber, et al.
Pageof 18