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Cell Transplantation|November 26, 2013
Stem cell salvage of injured peripheral nerveNadia Grimoldi, Federica Colleoni, Francesca Tiberio, et al.
Neurobiology of Aging|September 25, 2007
Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutationAnna Bersano, Roberto Del Bo, Costanza Lamperti, et al.
The Journal of Clinical Investigation|July 16, 2004
Human circulating AC133(+) stem cells restore dystrophin expression and ameliorate function in dystrophic skeletal muscleYvan Torrente, Marzia Belicchi, Maurilio Sampaolesi, et al.
BMC Medical Genetics|March 15, 2011
Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencingFrancesca Magri, Roberto Del Bo, Maria G D'Angelo, et al.
Human Genetics|July 8, 2011
Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysisRachele Cagliani, Matteo Fumagalli, Franca R Guerini, et al.
Neuromuscular Disorders : NMD|June 30, 2012
Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patientsFrancesca Magri, Roberto Del Bo, Maria Grazia D'Angelo, et al.
Cellular and Molecular Life Sciences : CMLS|March 14, 2022
Insights into the identification of a molecular signature for amyotrophic lateral sclerosis exploiting integrated microRNA profiling of iPSC-derived motor neurons and exosomesMafalda Rizzuti, Valentina Melzi, Delia Gagliardi, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|November 27, 2013
Decreased circulating miRNA levels in patients with primary progressive multiple sclerosisChiara Fenoglio, Elisa Ridolfi, Claudia Cantoni, et al.
American Journal of Human Genetics|May 5, 2009
The mitochondrial disulfide relay system protein GFER is mutated in autosomal-recessive myopathy with cataract and combined respiratory-chain deficiencyAlessio Di Fonzo, Dario Ronchi, Tiziana Lodi, et al.
Brain : a Journal of Neurology|October 9, 2012
Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletionsDario Ronchi, Caterina Garone, Andreina Bordoni, et al.
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