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Human Mutation|May 18, 2006
Hepatic and neuromuscular forms of glycogenosis type III: nine mutations in AGLS Lucchiari, S Pagliarani, S Salani, et al.
Neuro-Degenerative Diseases|February 12, 2011
Genetic background predicts poor prognosis in frontotemporal lobar degenerationB Borroni, M Grassi, S Archetti, et al.
Neuromuscular Disorders : NMD|December 7, 2002
Two dystrophin proteins and transcripts in a mild dystrophinopathic patientR Cagliani, A Bardoni, M Sironi, et al.
Neurology|April 26, 2001
Lack of apoptosis in mitochondrial encephalomyopathiesM Sciacco, G Fagiolari, C Lamperti, et al.
Scientific Reports|February 17, 2016
Morpholino-mediated SOD1 reduction ameliorates an amyotrophic lateral sclerosis disease phenotypeM Nizzardo, C Simone, F Rizzo, et al.
Cellular and Molecular Life Sciences : CMLS|March 7, 2001
T-antigen regulated expression reduces apoptosis of tag-transformed human myoblastsS Corti, S Salani, R Del Bo, et al.
The European Respiratory Journal|October 21, 2009
Abdominal volume contribution to tidal volume as an early indicator of respiratory impairment in Duchenne muscular dystrophyA Lo Mauro, M G D'Angelo, M Romei, et al.
Neuromuscular Disorders : NMD|December 18, 2003
Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian populationR Cagliani, F Fortunato, R Giorda, et al.
Human Molecular Genetics|August 1, 2000
Transplacental injection of somite-derived cells in mdx mouse embryos for the correction of dystrophin deficiencyY Torrente, M G D'Angelo, Z Li, et al.
Cell Transplantation|August 12, 1999
Extracorporeal circulation as a new experimental pathway for myoblast implantation in mdx miceY Torrente, M G D'Angelo, R Del Bo, et al.
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