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Annals of Clinical and Translational Neurology|April 16, 2016
Natural history of LGMD2A for delineating outcome measures in clinical trialsIsabelle Richard, Jean-Yves Hogrel, Daniel Stockholm, et al.
Archives of Physical Medicine and Rehabilitation|October 3, 2007
Comparison of a functional restoration program with active individual physical therapy for patients with chronic low back pain: a randomized controlled trialGhislaine Roche, Anne Ponthieux, Elsa Parot-Shinkel, et al.
Neuromuscular Disorders : NMD|October 25, 2008
Truncating mutations in C-terminal titin may cause more severe tibial muscular dystrophy (TMD)Peter Hackman, Sylvie Marchand, Jaakko Sarparanta, et al.
International Journal of Molecular Sciences|February 26, 2022
Co-Administration of Simvastatin Does Not Potentiate the Benefit of Gene Therapy in the mdx Mouse Model for Duchenne Muscular DystrophyNathalie Bourg, Ai Vu Hong, William Lostal, et al.
European Journal of Human Genetics : EJHG|February 5, 2015
Truncated prelamin A expression in HGPS-like patients: a transcriptional studyFlorian Barthélémy, Claire Navarro, Racha Fayek, et al.
Spine|March 19, 2011
Multidisciplinary intensive functional restoration versus outpatient active physiotherapy in chronic low back pain: a randomized controlled trialGhislaine Roche-Leboucher, Audrey Petit-Lemanac'h, Luc Bontoux, et al.
Free Radical Research|July 27, 2007
Oxidative stress implication in a new ex-vivo cardiac concordant xenotransplantation modelJean-Christophe Charniot, Dominique Bonnefont-Rousselot, Jean-Paul Albertini, et al.
JCI Insight|June 7, 2019
Dual muscle-liver transduction imposes immune tolerance for muscle transgene engraftment despite preexisting immunityLaurent Bartolo, Stéphanie Li Chung Tong, Pascal Chappert, et al.
Scientific Reports|May 8, 2019
Identification of thiostrepton as a pharmacological approach to rescue misfolded alpha-sarcoglycan mutant proteins from degradationLucile Hoch, Sara F Henriques, Celine Bruge, et al.
Human Molecular Genetics|June 20, 2013
Dysregulation of 4q35- and muscle-specific genes in fetuses with a short D4Z4 array linked to facio-scapulo-humeral dystrophyNatacha Broucqsault, Julia Morere, Marie-Cécile Gaillard, et al.
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