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Guillaume Bassez

Showing results (11-20 of 92) with videos related to

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Information Processing in Medical Imaging : Proceedings of the ... Conference|August 22, 2009
Clustering of the human skeletal muscle fibers using linear programming and angular Hilbertian metricsRadhouène Neji, Ahmed Besbes, Nikos Komodakis, et al.
Neuromuscular Disorders : NMD|April 9, 2008
Left ventricular non-compaction in a patient with myotonic dystrophy type 2Karim Wahbi, Christophe Meune, Guillaume Bassez, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|April 24, 2025
Key determinants of impaired gait performance in adults with neuromuscular diseases: a multiparametric and multimodal analysisRomain Feigean, Cylia Afroun-Roca, Cloé Guerrini, et al.
Neuromuscular Disorders : NMD|November 25, 2025
287th ENMC international workshop: Harmonization and federated analysis of myotonic dystrophy registries to model heterogeneous disease trajectories. Hoofddorp, the Netherlands, 28-30 March 2025Leandre A la Fontaine, Daniël van As, Guillaume Bassez, et al.
Neuromuscular Disorders : NMD|June 2, 2009
Left ventricular dysfunction and cardiac arrhythmias are frequent in type 2 myotonic dystrophy: a case control studyKarim Wahbi, Christophe Meune, Henri Marc Bécane, et al.
Medicine|January 26, 2019
Assessment of diaphragm motion using ultrasonography in a patient with facio-scapulo-humeral dystrophy: A case reportAbdallah Fayssoil, Tanya Stojkovic, Adam Ogna, et al.
Journal of Neuromuscular Diseases|January 8, 2026
Multiparametric assessment of the MyoSuit, a bi-articular exoskeleton designed to assist gait and transfers in adults with neuromuscular diseasesRomain Feigean, Cylia Afroun-Roca, Cloé Guerrini, et al.
Orphanet Journal of Rare Diseases|June 5, 2019
The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical careMarie De Antonio, Céline Dogan, Ferroudja Daidj, et al.
Journal of Neuropathology and Experimental Neurology|May 29, 2003
Inflammatory myopathy with abundant macrophages (IMAM): a condition sharing similarities with cytophagic histiocytic panniculitis and distinct from macrophagic myofasciitisGuillaume Bassez, Francois-Jérôme Authier, Emmanuèle Lechapt-Zalcman, et al.
Journal of Neuropathology and Experimental Neurology|April 2, 2008
Type 2 myotonic dystrophy can be predicted by the combination of type 2 muscle fiber central nucleation and scattered atrophyGuillaume Bassez, Elisabeth Chapoy, Sylvie Bastuji-Garin, et al.
Pageof 10

Showing results (11-20 of 92) with videos related to

Sort By:
Pageof 10
Information Processing in Medical Imaging : Proceedings of the ... Conference|August 22, 2009
Clustering of the human skeletal muscle fibers using linear programming and angular Hilbertian metricsRadhouène Neji, Ahmed Besbes, Nikos Komodakis, et al.
Neuromuscular Disorders : NMD|April 9, 2008
Left ventricular non-compaction in a patient with myotonic dystrophy type 2Karim Wahbi, Christophe Meune, Guillaume Bassez, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|April 24, 2025
Key determinants of impaired gait performance in adults with neuromuscular diseases: a multiparametric and multimodal analysisRomain Feigean, Cylia Afroun-Roca, Cloé Guerrini, et al.
Neuromuscular Disorders : NMD|November 25, 2025
287th ENMC international workshop: Harmonization and federated analysis of myotonic dystrophy registries to model heterogeneous disease trajectories. Hoofddorp, the Netherlands, 28-30 March 2025Leandre A la Fontaine, Daniël van As, Guillaume Bassez, et al.
Neuromuscular Disorders : NMD|June 2, 2009
Left ventricular dysfunction and cardiac arrhythmias are frequent in type 2 myotonic dystrophy: a case control studyKarim Wahbi, Christophe Meune, Henri Marc Bécane, et al.
Medicine|January 26, 2019
Assessment of diaphragm motion using ultrasonography in a patient with facio-scapulo-humeral dystrophy: A case reportAbdallah Fayssoil, Tanya Stojkovic, Adam Ogna, et al.
Journal of Neuromuscular Diseases|January 8, 2026
Multiparametric assessment of the MyoSuit, a bi-articular exoskeleton designed to assist gait and transfers in adults with neuromuscular diseasesRomain Feigean, Cylia Afroun-Roca, Cloé Guerrini, et al.
Orphanet Journal of Rare Diseases|June 5, 2019
The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical careMarie De Antonio, Céline Dogan, Ferroudja Daidj, et al.
Journal of Neuropathology and Experimental Neurology|May 29, 2003
Inflammatory myopathy with abundant macrophages (IMAM): a condition sharing similarities with cytophagic histiocytic panniculitis and distinct from macrophagic myofasciitisGuillaume Bassez, Francois-Jérôme Authier, Emmanuèle Lechapt-Zalcman, et al.
Journal of Neuropathology and Experimental Neurology|April 2, 2008
Type 2 myotonic dystrophy can be predicted by the combination of type 2 muscle fiber central nucleation and scattered atrophyGuillaume Bassez, Elisabeth Chapoy, Sylvie Bastuji-Garin, et al.
Pageof 10