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Pediatric Research|February 7, 2004
A new mitochondrial DNA mutation in ND3 gene causing severe Leigh syndrome with early lethalityMarco Crimi, Alexandros Papadimitriou, Sara Galbiati, et al.
Functional Neurology|April 20, 2013
Considerations on a mutation in the NOTCH3 gene sparing a cysteine residue: a rare polymorphism rather than a CADASIL variantAnna Bersano, Michela Ranieri, Andrea Ciammola, et al.
Neurogenetics|October 20, 2005
Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC)Maria T Bassi, Umberto Balottin, Chris Panzeri, et al.
Neurobiology of Aging|August 21, 2003
High mutational burden in the mtDNA control region from aged muscles: a single-fiber studyRoberto Del Bo, Marco Crimi, Monica Sciacco, et al.
Brain : a Journal of Neurology|April 19, 2007
Neural stem cells LewisX+ CXCR4+ modify disease progression in an amyotrophic lateral sclerosis modelStefania Corti, Federica Locatelli, Dimitra Papadimitriou, et al.
Neuroscience Letters|June 22, 2006
Candidate gene analysis of IP-10 gene in patients with Alzheimer's diseaseEliana Venturelli, Daniela Galimberti, Chiara Fenoglio, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 25, 2009
Motoneuron transplantation rescues the phenotype of SMARD1 (spinal muscular atrophy with respiratory distress type 1)Stefania Corti, Monica Nizzardo, Martina Nardini, et al.
Genome Biology|November 1, 2014
Genetic adaptation of the human circadian clock to day-length latitudinal variations and relevance for affective disordersDiego Forni, Uberto Pozzoli, Rachele Cagliani, et al.
Science Advances|November 25, 2015
Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse modelMonica Nizzardo, Chiara Simone, Federica Rizzo, et al.
Immunogenetics|March 2, 2006
VEGF gene variability and type 1 diabetes: evidence for a protective roleRoberto Del Bo, Marina Scarlato, Serena Ghezzi, et al.
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