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Annals of Clinical and Translational Neurology
|
June 26, 2024
Cardiac troponin T as a serum biomarker of respiratory impairment in amyotrophic lateral sclerosis
Teresa Koch, Rachel Fabian, Leonie Weinhold, et al.
Orphanet Journal of Rare Diseases
|
July 19, 2022
Short-term safety results from compassionate use of risdiplam in patients with spinal muscular atrophy in Germany
Andreas Hahn, René Günther, Albert Ludolph, et al.
Muscle & Nerve
|
February 12, 2025
Amyotrophic Lateral Sclerosis, the Endocannabinoid System, and Exogenous Cannabinoids: Current State and Clinical Implications
Travis T Denton, Gregory T Carter, Megan Goddard, et al.
Neuropharmacology
|
April 5, 2017
Evaluation of monoacylglycerol lipase as a therapeutic target in a transgenic mouse model of ALS
Noemi Pasquarelli, Michael Engelskirchen, Johannes Hanselmann, et al.
Plos One
|
August 22, 2014
Two-point magnitude MRI for rapid mapping of brown adipose tissue and its application to the R6/2 mouse model of Huntington disease
Katrin S Lindenberg, Patrick Weydt, Hans-Peter Müller, et al.
Human Molecular Genetics
|
May 17, 2012
A greatly extended PPARGC1A genomic locus encodes several new brain-specific isoforms and influences Huntington disease age of onset
Selma M Soyal, Thomas K Felder, Simon Auer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 10, 2017
Hypothalamic atrophy is related to body mass index and age at onset in amyotrophic lateral sclerosis
Martin Gorges, Pauline Vercruysse, Hans-Peter Müller, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 29, 2020
Deficits in verbal fluency in presymptomatic <i>C9orf72</i> mutation gene carriers-a developmental disorder
Dorothée E Lulé, Hans-Peter Müller, Julia Finsel, et al.
Journal of Molecular Neuroscience : MN
|
January 9, 2016
Towards a European Registry and Biorepository for Patients with Spinal and Bulbar Muscular Atrophy
Davide Pareyson, Pietro Fratta, Pierre-François Pradat, et al.
Plos One
|
April 14, 2017
High-resolution respirometry of fine-needle muscle biopsies in pre-manifest Huntington's disease expansion mutation carriers shows normal mitochondrial respiratory function
Eva Buck, Martina Zügel, Uwe Schumann, et al.
Page
of 11
Search research articles
Search
Showing results (41-50 of 108) with videos related to
Sort By:
Page
of 11
Annals of Clinical and Translational Neurology
|
June 26, 2024
Cardiac troponin T as a serum biomarker of respiratory impairment in amyotrophic lateral sclerosis
Teresa Koch, Rachel Fabian, Leonie Weinhold, et al.
Orphanet Journal of Rare Diseases
|
July 19, 2022
Short-term safety results from compassionate use of risdiplam in patients with spinal muscular atrophy in Germany
Andreas Hahn, René Günther, Albert Ludolph, et al.
Muscle & Nerve
|
February 12, 2025
Amyotrophic Lateral Sclerosis, the Endocannabinoid System, and Exogenous Cannabinoids: Current State and Clinical Implications
Travis T Denton, Gregory T Carter, Megan Goddard, et al.
Neuropharmacology
|
April 5, 2017
Evaluation of monoacylglycerol lipase as a therapeutic target in a transgenic mouse model of ALS
Noemi Pasquarelli, Michael Engelskirchen, Johannes Hanselmann, et al.
Plos One
|
August 22, 2014
Two-point magnitude MRI for rapid mapping of brown adipose tissue and its application to the R6/2 mouse model of Huntington disease
Katrin S Lindenberg, Patrick Weydt, Hans-Peter Müller, et al.
Human Molecular Genetics
|
May 17, 2012
A greatly extended PPARGC1A genomic locus encodes several new brain-specific isoforms and influences Huntington disease age of onset
Selma M Soyal, Thomas K Felder, Simon Auer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 10, 2017
Hypothalamic atrophy is related to body mass index and age at onset in amyotrophic lateral sclerosis
Martin Gorges, Pauline Vercruysse, Hans-Peter Müller, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 29, 2020
Deficits in verbal fluency in presymptomatic <i>C9orf72</i> mutation gene carriers-a developmental disorder
Dorothée E Lulé, Hans-Peter Müller, Julia Finsel, et al.
Journal of Molecular Neuroscience : MN
|
January 9, 2016
Towards a European Registry and Biorepository for Patients with Spinal and Bulbar Muscular Atrophy
Davide Pareyson, Pietro Fratta, Pierre-François Pradat, et al.
Plos One
|
April 14, 2017
High-resolution respirometry of fine-needle muscle biopsies in pre-manifest Huntington's disease expansion mutation carriers shows normal mitochondrial respiratory function
Eva Buck, Martina Zügel, Uwe Schumann, et al.
Page
of 11