Patrizia Barzaghi
Publications by Year
Research Areas
Muscle Physiology and Disorders, Cell Adhesion Molecules Research, Adipose Tissue and Metabolism, Cellular Mechanics and Interactions, Calpain Protease Function and Regulation
Most-Cited Works
- → An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy(2001)236 cited
- → Inhibition of synapse assembly in mammalian muscle in vivo by RNA interference(2004)130 cited
- → Overexpression of mini‐agrin in skeletal muscle increases muscle integrity and regenerative capacity in laminin‐α2‐deficient mice(2005)110 cited
- → Long-term blinded placebo-controlled study of SNT-MC17/idebenone in the dystrophin deficient mdx mouse: cardiac protection and improved exercise performance(2008)99 cited
- → Omigapil Ameliorates the Pathology of Muscle Dystrophy Caused by Laminin-α2 Deficiency(2009)86 cited
- → Linker molecules between laminins and dystroglycan ameliorate laminin-α2–deficient muscular dystrophy at all disease stages(2007)69 cited
- → Effect of calpain and proteasome inhibition on Ca 2+ ‐dependent proteolysis and muscle histopathology in the mdx mouse(2008)53 cited
- → Conjugation of LG Domains of Agrins and Perlecan to Polymerizing Laminin-2 Promotes Acetylcholine Receptor Clustering(2005)30 cited
- → T.O.3 SNT-MC17/idebenone in Duchenne muscular dystrophy: long-term blinded controlled preclinical study in the mdx mouse followed by a 12 month double-blind randomized controlled trial in humans(2008)3 cited
- → T.O.2 Omigapil/SNT-317 prevents apoptosis and ameliorates the pathology of laminin-alpha2 deficient muscle dystrophy(2008)