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American Journal of Physical Medicine & Rehabilitation|January 19, 2017
New Survival Target for Duchenne Muscular DystrophyMarcello Villanova, Sifa Kazibwe
American Journal of Physical Medicine & Rehabilitation|April 18, 2015
Allogeneic mesenchymal stem cell therapy outcomes for three patients with spinal muscular atrophy type 1Marcello Villanova, John Robert Bach
American Journal of Physical Medicine & Rehabilitation|April 19, 2014
Duchenne muscular dystrophy: life prolongation by noninvasive ventilatory supportMarcello Villanova, Beatrice Brancalion, Anokhi D Mehta
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|September 9, 2020
Respiratory muscle involvement in <i>HNRNPDL</i> LGMD D3 muscular dystrophy: an extensive clinical description of the first Italian patientEdoardo Malfatti, Denise Cassandrini, Anna Rubegni, et al.
Muscle & Nerve|March 14, 2003
Nerve growth factor expression in human dystrophic musclesPaolo Toti, Marcello Villanova, Rosella Vatti, et al.
Annals of Neurology|July 12, 2002
Electrophysiological findings in X-linked myopathy with excessive autophagySatu K Jääskeläinen, Vern C Juel, Bjarne Udd, et al.
European Journal of Human Genetics : EJHG|October 16, 2003
Phenylbutyrate increases SMN expression in vitro: relevance for treatment of spinal muscular atrophyCatia Andreassi, Carla Angelozzi, Francesco D Tiziano, et al.
Neuromuscular Disorders : NMD|June 27, 2008
Daily salbutamol in young patients with SMA type IIMarika Pane, Susanna Staccioli, Sonia Messina, et al.
Annals of Clinical and Translational Neurology|April 21, 2020
A new congenital multicore titinopathy associated with fast myosin heavy chain deficiencyAurélien Perrin, Corinne Metay, Marcello Villanova, et al.
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