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Molecular Genetics and Metabolism
|
January 22, 2013
Neutral lipid storage disease with myopathy: a whole-body nuclear MRI and metabolic study
Pascal 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 1
Linda 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 mosaicism
Stéphanie 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" syndrome
Guillaume 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 trial
Guillaume 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 dystrophy
Karim 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 growth
Bénédicte 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 mutations
Saïd 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 mexiletine
Savine 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 deficiency
Claire Wary, Pascal Laforêt, Bruno Eymard, et al.
Page
of 10
Search research articles
Search
Showing results (21-30 of 92) with videos related to
Sort By:
Page
of 10
Molecular Genetics and Metabolism
|
January 22, 2013
Neutral lipid storage disease with myopathy: a whole-body nuclear MRI and metabolic study
Pascal 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 1
Linda 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 mosaicism
Stéphanie 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" syndrome
Guillaume 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 trial
Guillaume 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 dystrophy
Karim 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 growth
Bénédicte 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 mutations
Saïd 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 mexiletine
Savine 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 deficiency
Claire Wary, Pascal Laforêt, Bruno Eymard, et al.
Page
of 10