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Acta Neuropathologica|February 18, 2020
Synaptotagmin 13 is neuroprotective across motor neuron diseasesM Nizzardo, M Taiana, F Rizzo, et al.Journal of Hematotherapy & Stem Cell Research|February 24, 2004
Neuronal differentiation of murine bone marrow Thy-1- and Sca-1-positive cellsF Locatelli, S Corti, C Donadoni, et al.Neurology|March 15, 2006
Coexistence of CMT-2D and distal SMA-V phenotypes in an Italian family with a GARS gene mutationR Del Bo, F Locatelli, S Corti, et al.Human Mutation|May 18, 2006
Hepatic and neuromuscular forms of glycogenosis type III: nine mutations in AGLS Lucchiari, S Pagliarani, S Salani, et al.Annals of Neurology|September 5, 2002
Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegiaEleonora Lamantea, Valeria Tiranti, Andreina Bordoni, et al.Neurology|April 26, 2001
Lack of apoptosis in mitochondrial encephalomyopathiesM Sciacco, G Fagiolari, C Lamperti, et al.Diabetes/Metabolism Research and Reviews|September 7, 2001
No evidence for SEL1L as a candidate gene for IDDM11-conferred susceptibilityF Pociot, Z M Larsen, P Zavattari, et al.Nucleic Acids Research|September 18, 2008
Cosegregation of novel mitochondrial 16S rRNA gene mutations with the age-associated T414G variant in human cybridsPeter Seibel, Chiara Di Nunno, Christian Kukat, 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.Neuro-Degenerative Diseases|February 12, 2011
Genetic background predicts poor prognosis in frontotemporal lobar degenerationB Borroni, M Grassi, S Archetti, et al.Pageof 35