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Experimental Cell Research|March 20, 2012
Direct reprogramming of human astrocytes into neural stem cells and neuronsStefania Corti, Monica Nizzardo, Chiara Simone, et al.
Science Translational Medicine|December 21, 2012
Genetic correction of human induced pluripotent stem cells from patients with spinal muscular atrophyStefania Corti, Monica Nizzardo, Chiara Simone, et al.
Journal of Biomedical Science|January 4, 2026
AAV9 gene therapy optimization for SMARD1/CMT2S: safety and long-term efficacy comparison of two vectors in a SMARD1 preclinical modelElisa Pagliari, Alessia Anastasia, Floriana Bellandi, et al.
The Journal of Clinical Investigation|September 5, 2008
Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophyStefania Corti, Monica Nizzardo, Martina Nardini, et al.
Brain : a Journal of Neurology|January 17, 2019
Key role of SMN/SYNCRIP and RNA-Motif 7 in spinal muscular atrophy: RNA-Seq and motif analysis of human motor neuronsFederica Rizzo, Monica Nizzardo, Shikha Vashisht, 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.
Progress in Neurobiology|April 27, 2020
miR-129-5p: A key factor and therapeutic target in amyotrophic lateral sclerosisAlessia Loffreda, Monica Nizzardo, Alessandro Arosio, 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.
Stem Cell Research|April 14, 2022
Generation of two hiPSC lines (UMILi027-A and UMILi028-A) from early and late-onset Congenital Central hypoventilation Syndrome (CCHS) patients carrying a polyalanine expansion mutation in the PHOX2B geneAna Lucia Cuadros Gamboa, Roberta Benfante, Monica Nizzardo, et al.
Cellular and Molecular Life Sciences : CMLS|November 25, 2023
Combined RNA interference and gene replacement therapy targeting MFN2 as proof of principle for the treatment of Charcot-Marie-Tooth type 2AFederica Rizzo, Silvia Bono, Marc David Ruepp, et al.
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