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Guillaume Bassez

Showing results (21-30 of 92) with videos related to

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Molecular Genetics and Metabolism|January 22, 2013
Neutral lipid storage disease with myopathy: a whole-body nuclear MRI and metabolic studyPascal Laforêt, Tanya Stojkovic, Guillaume Bassez, et al.
Radiology|August 19, 2020
Quantitative Muscle MRI Depicts Increased Muscle Mass after a Behavioral Change in Myotonic Dystrophy Type 1Linda Heskamp, Kees Okkersen, Marlies van Nimwegen, et al.
Human Mutation|April 18, 2018
Unusual association of a unique CAG interruption in 5' of DM1 CTG repeats with intergenerational contractions and low somatic mosaicismStéphanie Tomé, Elodie Dandelot, Céline Dogan, et al.
Neurobiology of Disease|March 10, 2004
Pleiotropic and diverse expression of ZFHX1B gene transcripts during mouse and human development supports the various clinical manifestations of the "Mowat-Wilson" syndromeGuillaume Bassez, Olivier J A Camand, Valère Cacheux, et al.
Brain : a Journal of Neurology|September 1, 2018
Improved mobility with metformin in patients with myotonic dystrophy type 1: a randomized controlled trialGuillaume Bassez, Etienne Audureau, Jean-Yves Hogrel, et al.
Archives of Cardiovascular Diseases|April 27, 2024
Expert opinion on mexiletine treatment in adult patients with myotonic dystrophyKarim Wahbi, Guillaume Bassez, Josselin Duchateau, et al.
The Journal of Cell Biology|December 10, 2003
Satellite cells attract monocytes and use macrophages as a support to escape apoptosis and enhance muscle growthBénédicte Chazaud, Corinne Sonnet, Peggy Lafuste, et al.
The Journal of Physiology|April 16, 2005
In vivo and in vitro functional characterization of Andersen's syndrome mutationsSaïd Bendahhou, Emmanuel Fournier, Damien Sternberg, et al.
Neuromuscular Disorders : NMD|October 5, 2024
Recommendations of an expert group for the cardiac assessment of non-dystrophic myotonia adult patients treated with mexiletineSavine Vicart, Karim Wahbi, Josselin Duchateau, et al.
Neuromuscular Disorders : NMD|August 19, 2003
Evaluation of muscle glycogen content by 13C NMR spectroscopy in adult-onset acid maltase deficiencyClaire Wary, Pascal Laforêt, Bruno Eymard, et al.
Pageof 10

Showing results (21-30 of 92) with videos related to

Sort By:
Pageof 10
Molecular Genetics and Metabolism|January 22, 2013
Neutral lipid storage disease with myopathy: a whole-body nuclear MRI and metabolic studyPascal Laforêt, Tanya Stojkovic, Guillaume Bassez, et al.
Radiology|August 19, 2020
Quantitative Muscle MRI Depicts Increased Muscle Mass after a Behavioral Change in Myotonic Dystrophy Type 1Linda Heskamp, Kees Okkersen, Marlies van Nimwegen, et al.
Human Mutation|April 18, 2018
Unusual association of a unique CAG interruption in 5' of DM1 CTG repeats with intergenerational contractions and low somatic mosaicismStéphanie Tomé, Elodie Dandelot, Céline Dogan, et al.
Neurobiology of Disease|March 10, 2004
Pleiotropic and diverse expression of ZFHX1B gene transcripts during mouse and human development supports the various clinical manifestations of the "Mowat-Wilson" syndromeGuillaume Bassez, Olivier J A Camand, Valère Cacheux, et al.
Brain : a Journal of Neurology|September 1, 2018
Improved mobility with metformin in patients with myotonic dystrophy type 1: a randomized controlled trialGuillaume Bassez, Etienne Audureau, Jean-Yves Hogrel, et al.
Archives of Cardiovascular Diseases|April 27, 2024
Expert opinion on mexiletine treatment in adult patients with myotonic dystrophyKarim Wahbi, Guillaume Bassez, Josselin Duchateau, et al.
The Journal of Cell Biology|December 10, 2003
Satellite cells attract monocytes and use macrophages as a support to escape apoptosis and enhance muscle growthBénédicte Chazaud, Corinne Sonnet, Peggy Lafuste, et al.
The Journal of Physiology|April 16, 2005
In vivo and in vitro functional characterization of Andersen's syndrome mutationsSaïd Bendahhou, Emmanuel Fournier, Damien Sternberg, et al.
Neuromuscular Disorders : NMD|October 5, 2024
Recommendations of an expert group for the cardiac assessment of non-dystrophic myotonia adult patients treated with mexiletineSavine Vicart, Karim Wahbi, Josselin Duchateau, et al.
Neuromuscular Disorders : NMD|August 19, 2003
Evaluation of muscle glycogen content by 13C NMR spectroscopy in adult-onset acid maltase deficiencyClaire Wary, Pascal Laforêt, Bruno Eymard, et al.
Pageof 10