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Cell Cycle (Georgetown, Tex.)|July 22, 2008
Aquaporin-4 expression is severely reduced in human sarcoglycanopathies and dysferlinopathiesStefania Assereto, Mauro Mastrototaro, Silvia Stringara, et al.
Pharmaceuticals (Basel, Switzerland)|January 21, 2022
P2X7 Receptor Antagonist Reduces Fibrosis and Inflammation in a Mouse Model of Alpha-Sarcoglycan Muscular DystrophyLizzia Raffaghello, Elisa Principi, Serena Baratto, et al.
Current Neurology and Neuroscience Reports|January 22, 2013
Neuromuscular disorders of glycogen metabolismElisabetta Gazzerro, Antoni L Andreu, Claudio Bruno
Endocrine Reviews|April 18, 2003
Bone morphogenetic proteins, their antagonists, and the skeletonErnesto Canalis, Aris N Economides, Elisabetta Gazzerro
Nature Reviews. Neurology|August 7, 2010
Epilepsy: old drugs do the trick in childhood absence epilepsyPasquale Striano, Carlo Minetti
Current Neurology and Neuroscience Reports|December 20, 2003
Congenital myopathiesClaudio Bruno, Carlo Minetti
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 20, 2010
The spectrum of GNE mutations: allelic heterogeneity for a common phenotypeMarina Grandis, Rossella Gulli, Denise Cassandrini, et al.
Journal of Human Genetics|March 21, 2018
Clinical and molecular consequences of exon 78 deletion in DMD geneMonica Traverso, Stefania Assereto, Serena Baratto, et al.
Annals of Neurology|May 1, 2014
Impairment of ceramide synthesis causes a novel progressive myoclonus epilepsyNicola Vanni, Floriana Fruscione, Edoardo Ferlazzo, et al.
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