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Pascal Cintas

Showing results (31-40 of 80) with videos related to

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Clinical Neurology and Neurosurgery|May 9, 2026
Feasibility and usefulness of personalised patient-reported outcome measures in the therapeutic follow-up of adult spinal muscular atrophy patientsPascal Cintas, Samuel Pouplin, Louise Debergé, et al.
European Journal of Radiology|May 4, 2024
Assessment of whole-body muscle MRI for the early diagnosis of Amyotrophic Lateral SclerosisRokia El Khalfi, Estelle Maupoint, Hélène Chiavassa-Gandois, et al.
Biomedicines|February 24, 2024
The <i>FLNC</i> Ala1186Val Variant Linked to Cytoplasmic Body Myopathy and Cardiomyopathy Causes Protein InstabilityMarion Onnée, Audrey Bénézit, Sultan Bastu, et al.
Frontiers in Cardiovascular Medicine|December 17, 2021
New Oral Anticoagulants vs. Vitamin K Antagonists Among Patients With Cardiac Amyloidosis: Prognostic ImpactEve Cariou, Kevin Sanchis, Khailène Rguez, et al.
The Journal of Infection|July 4, 2018
Acute hepatitis E in French patients and neurological manifestationsFlorence Abravanel, Julie Pique, Elisabeth Couturier, et al.
Bulletin Du Cancer|December 11, 2019
[Indication of autologous stem cell transplantation in chronic inflammatory demyelinating polyneuropathy: Guidelines from the Francophone Society of Bone Marrow Transplantation and Cellular Therapy (SFGM-TC)]Mathieu Puyade, Céline Labeyrie, Manuela Badoglio, et al.
International Journal of Molecular Sciences|March 27, 2020
Type 1 FSHD with 6-10 Repeated Units: Factors Underlying Severity in Index Cases and Disease Penetrance in Their Relatives AttentionEmmanuelle Salort-Campana, Farzad Fatehi, Sadia Beloribi-Djefaflia, et al.
Neuromuscular Disorders : NMD|April 23, 2016
Unusual association of amyotrophic lateral sclerosis and myasthenia gravis: A dysregulation of the adaptive immune system?Maria Del Mar Amador, Nadia Vandenberghe, Nawel Berhoune, et al.
Muscle & Nerve|April 14, 2017
Hereditary neuropathy with liability to pressure palsy in patients under 30 years old: Neurophysiological data and proposed electrodiagnostic criteriaFlorence Robert-Varvat, Guillemette Jousserand, Françoise Bouhour, et al.
Orphanet Journal of Rare Diseases|March 3, 2022
Convergence of patient- and physician-reported outcomes in the French National Registry of Facioscapulohumeral DystrophyBenoît Sanson, Caroline Stalens, Céline Guien, et al.
Pageof 8

Showing results (31-40 of 80) with videos related to

Sort By:
Pageof 8
Clinical Neurology and Neurosurgery|May 9, 2026
Feasibility and usefulness of personalised patient-reported outcome measures in the therapeutic follow-up of adult spinal muscular atrophy patientsPascal Cintas, Samuel Pouplin, Louise Debergé, et al.
European Journal of Radiology|May 4, 2024
Assessment of whole-body muscle MRI for the early diagnosis of Amyotrophic Lateral SclerosisRokia El Khalfi, Estelle Maupoint, Hélène Chiavassa-Gandois, et al.
Biomedicines|February 24, 2024
The <i>FLNC</i> Ala1186Val Variant Linked to Cytoplasmic Body Myopathy and Cardiomyopathy Causes Protein InstabilityMarion Onnée, Audrey Bénézit, Sultan Bastu, et al.
Frontiers in Cardiovascular Medicine|December 17, 2021
New Oral Anticoagulants vs. Vitamin K Antagonists Among Patients With Cardiac Amyloidosis: Prognostic ImpactEve Cariou, Kevin Sanchis, Khailène Rguez, et al.
The Journal of Infection|July 4, 2018
Acute hepatitis E in French patients and neurological manifestationsFlorence Abravanel, Julie Pique, Elisabeth Couturier, et al.
Bulletin Du Cancer|December 11, 2019
[Indication of autologous stem cell transplantation in chronic inflammatory demyelinating polyneuropathy: Guidelines from the Francophone Society of Bone Marrow Transplantation and Cellular Therapy (SFGM-TC)]Mathieu Puyade, Céline Labeyrie, Manuela Badoglio, et al.
International Journal of Molecular Sciences|March 27, 2020
Type 1 FSHD with 6-10 Repeated Units: Factors Underlying Severity in Index Cases and Disease Penetrance in Their Relatives AttentionEmmanuelle Salort-Campana, Farzad Fatehi, Sadia Beloribi-Djefaflia, et al.
Neuromuscular Disorders : NMD|April 23, 2016
Unusual association of amyotrophic lateral sclerosis and myasthenia gravis: A dysregulation of the adaptive immune system?Maria Del Mar Amador, Nadia Vandenberghe, Nawel Berhoune, et al.
Muscle & Nerve|April 14, 2017
Hereditary neuropathy with liability to pressure palsy in patients under 30 years old: Neurophysiological data and proposed electrodiagnostic criteriaFlorence Robert-Varvat, Guillemette Jousserand, Françoise Bouhour, et al.
Orphanet Journal of Rare Diseases|March 3, 2022
Convergence of patient- and physician-reported outcomes in the French National Registry of Facioscapulohumeral DystrophyBenoît Sanson, Caroline Stalens, Céline Guien, et al.
Pageof 8