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Brain : a Journal of Neurology
|
December 23, 2011
The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype
Cécile Rouzier, Sylvie Bannwarth, Annabelle Chaussenot, et al.
Neurophysiologie Clinique = Clinical Neurophysiology
|
July 31, 2025
Is the decrement pattern in myasthenia gravis due to muscle-specific kinase antibodies different to that due to acetylcholine receptor antibodies?
Antoine Pegat, Antoine Gavoille, Maxime Bonjour, et al.
BMJ Open
|
October 31, 2018
Molecular diagnosis of inherited peripheral neuropathies by targeted next-generation sequencing: molecular spectrum delineation
Juliette Bacquet, Tanya Stojkovic, Amandine Boyer, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
|
November 16, 2010
Safety of home parenteral nutrition in patients with amyotrophic lateral sclerosis: a French national survey
Maya Abdelnour-Mallet, Annie Verschueren, Nathalie Guy, et al.
International Journal of Molecular Sciences
|
August 14, 2025
Improving ALS Molecular Diagnosis Through Functional Assays: Reassessment of a <i>SOD1</i> Variant of Uncertain Significance
Léa Bedja-Iacona, Arthur Forget, Chloé Boisseau, et al.
American Journal of Human Genetics
|
September 1, 2009
Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy
Lucie Gueneau, Anne T Bertrand, Jean-Philippe Jais, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
August 29, 2021
Assessing the upper motor neuron in amyotrophic lateral sclerosis using the triple stimulation technique: A multicenter prospective study
Aude-Marie Grapperon, Annie Verschueren, Elisabeth Jouve, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
July 25, 2020
Motor unit number index as an individual biomarker: Reference limits of intra-individual variability over time in healthy subjects
Emilien Delmont, François Wang, Jean-Pascal Lefaucheur, et al.
Brain : a Journal of Neurology
|
June 18, 2014
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement
Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 31, 2021
Impact of a frequent nearsplice <i>SOD1</i> variant in amyotrophic lateral sclerosis: optimising <i>SOD1</i> genetic screening for gene therapy opportunities
François Muratet, Elisa Teyssou, Aude Chiot, et al.
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of 6
Search research articles
Search
Showing results (41-50 of 57) with videos related to
Sort By:
Page
of 6
Brain : a Journal of Neurology
|
December 23, 2011
The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype
Cécile Rouzier, Sylvie Bannwarth, Annabelle Chaussenot, et al.
Neurophysiologie Clinique = Clinical Neurophysiology
|
July 31, 2025
Is the decrement pattern in myasthenia gravis due to muscle-specific kinase antibodies different to that due to acetylcholine receptor antibodies?
Antoine Pegat, Antoine Gavoille, Maxime Bonjour, et al.
BMJ Open
|
October 31, 2018
Molecular diagnosis of inherited peripheral neuropathies by targeted next-generation sequencing: molecular spectrum delineation
Juliette Bacquet, Tanya Stojkovic, Amandine Boyer, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
|
November 16, 2010
Safety of home parenteral nutrition in patients with amyotrophic lateral sclerosis: a French national survey
Maya Abdelnour-Mallet, Annie Verschueren, Nathalie Guy, et al.
International Journal of Molecular Sciences
|
August 14, 2025
Improving ALS Molecular Diagnosis Through Functional Assays: Reassessment of a <i>SOD1</i> Variant of Uncertain Significance
Léa Bedja-Iacona, Arthur Forget, Chloé Boisseau, et al.
American Journal of Human Genetics
|
September 1, 2009
Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy
Lucie Gueneau, Anne T Bertrand, Jean-Philippe Jais, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
August 29, 2021
Assessing the upper motor neuron in amyotrophic lateral sclerosis using the triple stimulation technique: A multicenter prospective study
Aude-Marie Grapperon, Annie Verschueren, Elisabeth Jouve, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
July 25, 2020
Motor unit number index as an individual biomarker: Reference limits of intra-individual variability over time in healthy subjects
Emilien Delmont, François Wang, Jean-Pascal Lefaucheur, et al.
Brain : a Journal of Neurology
|
June 18, 2014
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement
Sylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 31, 2021
Impact of a frequent nearsplice <i>SOD1</i> variant in amyotrophic lateral sclerosis: optimising <i>SOD1</i> genetic screening for gene therapy opportunities
François Muratet, Elisa Teyssou, Aude Chiot, et al.
Page
of 6