Gianna Ulzi

Glycogen storage disease type III: A novel Agl knockout mouse model.

N. Bresolin, G. Comi, S. Corti, 2014, Biochimica et biophysica acta.

In vitro analysis of splice site mutations in the CLCN1 gene using the minigene assay

N. Bresolin, G. Comi, S. Corti, 2014, Molecular Biology Reports.

Spinal muscular atrophy phenotype is ameliorated in human motor neurons by SMN increase via different novel RNA therapeutic approaches

S. Salani, F. Rizzo, N. Bresolin, 2015, Scientific Reports.

Clinical evaluation and cellular electrophysiology of a recessive CLCN1 patient.

M. Moggio, M. Lecchi, F. Magri, 2013, Journal of physiology and pharmacology : an official journal of the Polish Physiological Society.

Morpholino-mediated SOD1 reduction ameliorates an amyotrophic lateral sclerosis disease phenotype

F. Rizzo, N. Bresolin, G. Comi, 2016, Scientific Reports.

In vitro analysis of splice site mutations in the CLCN1 gene using the minigene assay

N. Bresolin, G. Comi, S. Corti, 2014, Molecular Biology Reports.

Myotonia congenita: Novel mutations in CLCN1 gene and functional characterizations in Italian patients

N. Bresolin, S. Corti, E. Redaelli, 2012, Journal of the Neurological Sciences.