Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Guillaume Bassez

Showing results (31-40 of 92) with videos related to

Pageof 10
Sort By:
Respiratory Medicine and Research|June 11, 2026
Determinants of diaphragm ultrasound and its diagnostic performance for predicting respiratory status in myotonic dystrophy type 1Abdallah Fayssoil, Marie De Antonio, Helene Prigent, et al.
European Journal of Heart Failure|November 30, 2005
Severe dilated cardiomyopathy and quadriceps myopathy due to lamin A/C gene mutation: a phenotypic studyJean-Christophe Charniot, Michel Desnos, Khaled Zerhouni, et al.
Muscle & Nerve|January 17, 2020
Brody myopathy demonstrates a pseudo-increment on repetitive nerve stimulationMarion Masingue, Marianne Arzel, Damien Sternberg, et al.
Molecular Biology of the Cell|February 9, 2007
Muscle satellite cells and endothelial cells: close neighbors and privileged partnersChristo Christov, Fabrice Chrétien, Rana Abou-Khalil, et al.
Journal of Neuromuscular Diseases|July 12, 2021
Clinical Outcome Evaluations and CBT Response Prediction in Myotonic DystrophyDaniël van As, Kees Okkersen, Guillaume Bassez, et al.
Muscle & Nerve|May 29, 2026
Psychosocial Determinants of Pain in Muscle BiopsyBeatrice Labella, Emmanuelle Lacene, Maud Beuvin, et al.
Neurology|May 24, 2019
Lower extremity muscle pathology in myotonic dystrophy type 1 assessed by quantitative MRILinda Heskamp, Marlies van Nimwegen, Marieke J Ploegmakers, et al.
Human Mutation|July 13, 2005
Dysferlin mutations in LGMD2B, Miyoshi myopathy, and atypical dysferlinopathiesKarine Nguyen, Guillaume Bassez, Rafaëlle Bernard, et al.
Neuromuscular Disorders : NMD|March 8, 2016
Atrial flutter in myotonic dystrophy type 1: Patient characteristics and clinical outcomeKarim Wahbi, Frederic A Sebag, Nicolas Lellouche, et al.
Genomics, Proteomics & Bioinformatics|October 24, 2025
Comparative Analysis of CRISPR/Cas9-targeted Nanopore Sequencing Approaches in Repeat Expansion DisordersLouise Benarroch, Pierre-Yves Boëlle, Hélène Madry, et al.
Pageof 10

Showing results (31-40 of 92) with videos related to

Sort By:
Pageof 10
Respiratory Medicine and Research|June 11, 2026
Determinants of diaphragm ultrasound and its diagnostic performance for predicting respiratory status in myotonic dystrophy type 1Abdallah Fayssoil, Marie De Antonio, Helene Prigent, et al.
European Journal of Heart Failure|November 30, 2005
Severe dilated cardiomyopathy and quadriceps myopathy due to lamin A/C gene mutation: a phenotypic studyJean-Christophe Charniot, Michel Desnos, Khaled Zerhouni, et al.
Muscle & Nerve|January 17, 2020
Brody myopathy demonstrates a pseudo-increment on repetitive nerve stimulationMarion Masingue, Marianne Arzel, Damien Sternberg, et al.
Molecular Biology of the Cell|February 9, 2007
Muscle satellite cells and endothelial cells: close neighbors and privileged partnersChristo Christov, Fabrice Chrétien, Rana Abou-Khalil, et al.
Journal of Neuromuscular Diseases|July 12, 2021
Clinical Outcome Evaluations and CBT Response Prediction in Myotonic DystrophyDaniël van As, Kees Okkersen, Guillaume Bassez, et al.
Muscle & Nerve|May 29, 2026
Psychosocial Determinants of Pain in Muscle BiopsyBeatrice Labella, Emmanuelle Lacene, Maud Beuvin, et al.
Neurology|May 24, 2019
Lower extremity muscle pathology in myotonic dystrophy type 1 assessed by quantitative MRILinda Heskamp, Marlies van Nimwegen, Marieke J Ploegmakers, et al.
Human Mutation|July 13, 2005
Dysferlin mutations in LGMD2B, Miyoshi myopathy, and atypical dysferlinopathiesKarine Nguyen, Guillaume Bassez, Rafaëlle Bernard, et al.
Neuromuscular Disorders : NMD|March 8, 2016
Atrial flutter in myotonic dystrophy type 1: Patient characteristics and clinical outcomeKarim Wahbi, Frederic A Sebag, Nicolas Lellouche, et al.
Genomics, Proteomics & Bioinformatics|October 24, 2025
Comparative Analysis of CRISPR/Cas9-targeted Nanopore Sequencing Approaches in Repeat Expansion DisordersLouise Benarroch, Pierre-Yves Boëlle, Hélène Madry, et al.
Pageof 10