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Research in Developmental Disabilities|April 16, 2013
Effect of observation of simple hand movement on brain activations in patients with unilateral cerebral palsy: an fMRI studyMickael Dinomais, Gregoire Lignon, Eva Chinier, et al.
Molecular Therapy. Methods & Clinical Development|June 2, 2015
A comparison of AAV strategies distinguishes overlapping vectors for efficient systemic delivery of the 6.2 kb Dysferlin coding sequenceMarina Pryadkina, William Lostal, Nathalie Bourg, et al.
Human Mutation|June 20, 2020
A single c.1715G>C calpain 3 gene variant causes dominant calpainopathy with loss of calpain 3 expression and activityJohn Vissing, Julia R Dahlqvist, Carinne Roudaut, et al.
Presse Medicale (Paris, France : 1983)|June 17, 2011
[Improving the level of understanding of English of medical students is possible. Results of a systematic assessment policy]Léa Lebrun, Martine Fisbach, Jérôme Febvre, et al.
Muscle & Nerve|October 21, 2016
γ-sarcoglycan and dystrophin mutation spectrum in an Algerian cohortImene Dalichaouche, Yamina Sifi, Carinne Roudaut, et al.
Thrombosis Research|January 8, 2008
S35225 is a direct inhibitor of Plasminogen Activator Inhibitor type-1 activity in the bloodAlain Rupin, Roger Gaertner, Philippe Mennecier, et al.
Neuromuscular Disorders : NMD|March 20, 2021
Late-onset camptocormia caused by a heterozygous in-frame CAPN3 deletionMarco Spinazzi, Jerome Poupiot, Julien Cassereau, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 1, 2021
Identification of novel mutations by targeted NGS in Moroccan families clinically diagnosed with a neuromuscular disorderKhaoula Rochdi, Mathieu Cerino, Nathalie Da Silva, et al.
Neuropsychologia|May 9, 2008
Different constraints on grip selection in brain-damaged patients: object use versus object transportFrançois Osiurak, Ghislaine Aubin, Philippe Allain, et al.
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