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The Journal of Clinical Investigation
|
November 6, 2025
Early brain-wide disruption of sleep microarchitecture in amyotrophic lateral sclerosis
Christina Lang, Simon J Guillot, Dorothee Lule, et al.
Human Molecular Genetics
|
May 15, 2013
PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis
Judith Eschbach, Birgit Schwalenstöcker, Selma M Soyal, et al.
Neurobiology of Disease
|
November 8, 2016
ALS-causing mutations differentially affect PGC-1α expression and function in the brain vs. peripheral tissues
Hanna Bayer, Kerstin Lang, Eva Buck, et al.
Frontiers in Neurology
|
December 3, 2019
Routine Cerebrospinal Fluid (CSF) Parameters in Patients With Spinal Muscular Atrophy (SMA) Treated With Nusinersen
Claudia D Wurster, Jan C Koch, Isabell Cordts, et al.
Neurological Research and Practice
|
August 23, 2024
User expectations and experiences of an assistive robotic arm in amyotrophic lateral sclerosis: a multicenter observational study
Susanne Spittel, Thomas Meyer, Ute Weyen, et al.
Muscle & Nerve
|
March 17, 2023
Neurofilament light-chain response during therapy with antisense oligonucleotide tofersen in SOD1-related ALS: Treatment experience in clinical practice
Thomas Meyer, Peggy Schumann, Patrick Weydt, et al.
Journal of Alzheimer'S Disease : JAD
|
July 22, 2017
Novel Blood-Based Biomarkers of Cognition, Stress, and Physical or Cognitive Training in Older Adults at Risk of Dementia: Preliminary Evidence for a Role of BDNF, Irisin, and the Kynurenine Pathway
Olivia C Küster, Daria Laptinskaya, Patrick Fissler, 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 dysfunction
Thomas Meyer, Matthias Boentert, Julian Großkreutz, et al.
Journal of Neurology
|
February 22, 2018
The metabolic and endocrine characteristics in spinal and bulbar muscular atrophy
Angela Rosenbohm, Susanne Hirsch, Alexander E Volk, et al.
Brain : a Journal of Neurology
|
September 7, 2014
Serum microRNAs in patients with genetic amyotrophic lateral sclerosis and pre-manifest mutation carriers
Axel Freischmidt, Kathrin Müller, Lisa Zondler, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 108) with videos related to
Sort By:
Page
of 11
The Journal of Clinical Investigation
|
November 6, 2025
Early brain-wide disruption of sleep microarchitecture in amyotrophic lateral sclerosis
Christina Lang, Simon J Guillot, Dorothee Lule, et al.
Human Molecular Genetics
|
May 15, 2013
PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis
Judith Eschbach, Birgit Schwalenstöcker, Selma M Soyal, et al.
Neurobiology of Disease
|
November 8, 2016
ALS-causing mutations differentially affect PGC-1α expression and function in the brain vs. peripheral tissues
Hanna Bayer, Kerstin Lang, Eva Buck, et al.
Frontiers in Neurology
|
December 3, 2019
Routine Cerebrospinal Fluid (CSF) Parameters in Patients With Spinal Muscular Atrophy (SMA) Treated With Nusinersen
Claudia D Wurster, Jan C Koch, Isabell Cordts, et al.
Neurological Research and Practice
|
August 23, 2024
User expectations and experiences of an assistive robotic arm in amyotrophic lateral sclerosis: a multicenter observational study
Susanne Spittel, Thomas Meyer, Ute Weyen, et al.
Muscle & Nerve
|
March 17, 2023
Neurofilament light-chain response during therapy with antisense oligonucleotide tofersen in SOD1-related ALS: Treatment experience in clinical practice
Thomas Meyer, Peggy Schumann, Patrick Weydt, et al.
Journal of Alzheimer'S Disease : JAD
|
July 22, 2017
Novel Blood-Based Biomarkers of Cognition, Stress, and Physical or Cognitive Training in Older Adults at Risk of Dementia: Preliminary Evidence for a Role of BDNF, Irisin, and the Kynurenine Pathway
Olivia C Küster, Daria Laptinskaya, Patrick Fissler, 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 dysfunction
Thomas Meyer, Matthias Boentert, Julian Großkreutz, et al.
Journal of Neurology
|
February 22, 2018
The metabolic and endocrine characteristics in spinal and bulbar muscular atrophy
Angela Rosenbohm, Susanne Hirsch, Alexander E Volk, et al.
Brain : a Journal of Neurology
|
September 7, 2014
Serum microRNAs in patients with genetic amyotrophic lateral sclerosis and pre-manifest mutation carriers
Axel Freischmidt, Kathrin Müller, Lisa Zondler, et al.
Page
of 11