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Guillaume Bassez

Showing results (51-60 of 92) with videos related to

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Muscle & Nerve|February 7, 2017
The quality of life in genetic neuromuscular disease questionnaire: Rasch validation of the French versionAntoine Dany, Amandine Rapin, Brice Lavrard, et al.
BMC Neurology|June 16, 2026
Exploring the impact of myotonia on daily functioning in myotonic dystrophy: a patient-reported surveyValeria A Sansone, Utkarsh J Dang, Linda Edmondson, et al.
Neurology. Clinical Practice|October 5, 2019
Consensus-based care recommendations for adults with myotonic dystrophy type 2Benedikt Schoser, Federica Montagnese, Guillaume Bassez, et al.
Rheumatology (Oxford, England)|February 24, 2018
Muscle ischaemia associated with NXP2 autoantibodies: a severe subtype of juvenile dermatomyositisJessie Aouizerate, Marie De Antonio, Brigitte Bader-Meunier, et al.
Circulation. Cardiovascular Genetics|June 15, 2017
Association Between Mutation Size and Cardiac Involvement in Myotonic Dystrophy Type 1: An Analysis of the DM1-Heart RegistryCaroline Chong-Nguyen, Karim Wahbi, Vincent Algalarrondo, et al.
Neurology. Genetics|April 22, 2021
Associations Between Variant Repeat Interruptions and Clinical Outcomes in Myotonic Dystrophy Type 1Stephan Wenninger, Sarah A Cumming, Kristina Gutschmidt, et al.
Journal of Neuromuscular Diseases|April 5, 2021
Improved Cardiac Outcomes by Early Treatment with Angiotensin-Converting Enzyme Inhibitors in Becker Muscular DystrophyCaroline Stalens, Leslie Motté, Anthony Béhin, et al.
Plos One|April 25, 2019
Diaphragm sniff ultrasound: Normal values, relationship with sniff nasal pressure and accuracy for predicting respiratory involvement in patients with neuromuscular disordersAbdallah Fayssoil, Lee S Nguyen, Adam Ogna, et al.
Neurology|January 19, 2018
Hearing impairment in patients with myotonic dystrophy type 2Judith van Vliet, Alide A Tieleman, Baziel G M van Engelen, et al.
Plos Genetics|December 5, 2012
Molecular, physiological, and motor performance defects in DMSXL mice carrying >1,000 CTG repeats from the human DM1 locusAline Huguet, Fadia Medja, Annie Nicole, et al.
Pageof 10

Showing results (51-60 of 92) with videos related to

Sort By:
Pageof 10
Muscle & Nerve|February 7, 2017
The quality of life in genetic neuromuscular disease questionnaire: Rasch validation of the French versionAntoine Dany, Amandine Rapin, Brice Lavrard, et al.
BMC Neurology|June 16, 2026
Exploring the impact of myotonia on daily functioning in myotonic dystrophy: a patient-reported surveyValeria A Sansone, Utkarsh J Dang, Linda Edmondson, et al.
Neurology. Clinical Practice|October 5, 2019
Consensus-based care recommendations for adults with myotonic dystrophy type 2Benedikt Schoser, Federica Montagnese, Guillaume Bassez, et al.
Rheumatology (Oxford, England)|February 24, 2018
Muscle ischaemia associated with NXP2 autoantibodies: a severe subtype of juvenile dermatomyositisJessie Aouizerate, Marie De Antonio, Brigitte Bader-Meunier, et al.
Circulation. Cardiovascular Genetics|June 15, 2017
Association Between Mutation Size and Cardiac Involvement in Myotonic Dystrophy Type 1: An Analysis of the DM1-Heart RegistryCaroline Chong-Nguyen, Karim Wahbi, Vincent Algalarrondo, et al.
Neurology. Genetics|April 22, 2021
Associations Between Variant Repeat Interruptions and Clinical Outcomes in Myotonic Dystrophy Type 1Stephan Wenninger, Sarah A Cumming, Kristina Gutschmidt, et al.
Journal of Neuromuscular Diseases|April 5, 2021
Improved Cardiac Outcomes by Early Treatment with Angiotensin-Converting Enzyme Inhibitors in Becker Muscular DystrophyCaroline Stalens, Leslie Motté, Anthony Béhin, et al.
Plos One|April 25, 2019
Diaphragm sniff ultrasound: Normal values, relationship with sniff nasal pressure and accuracy for predicting respiratory involvement in patients with neuromuscular disordersAbdallah Fayssoil, Lee S Nguyen, Adam Ogna, et al.
Neurology|January 19, 2018
Hearing impairment in patients with myotonic dystrophy type 2Judith van Vliet, Alide A Tieleman, Baziel G M van Engelen, et al.
Plos Genetics|December 5, 2012
Molecular, physiological, and motor performance defects in DMSXL mice carrying >1,000 CTG repeats from the human DM1 locusAline Huguet, Fadia Medja, Annie Nicole, et al.
Pageof 10