Alessia Arnoldi

Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot–Marie–Tooth type 2

Claudia Crimella, Cinzia Baschirotto, Alessia Arnoldi et al. · Clinical Genetics · 2011 · 156 citations

Genetics, Molecular Genetics, Disease Gene Identification +17

Hereditary spastic paraplegia type 5: natural history, biomarkers and a randomized controlled trial

Lüdger Schöls, Tim W. Rattay, Peter Martus et al. · Brain · 2017 · 104 citations · Full text

A clinical, genetic, and biochemical characterization of<i>SPG7</i>mutations in a large cohort of patients with hereditary spastic paraplegia

Alessia Arnoldi, Alessandra Tonelli, Francesca Crippa et al. · Human Mutation · 2008 · 100 citations

Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis

Andrea Citterio, Alessia Arnoldi, Elena Panzeri et al. · Journal of Neurology · 2013 · 69 citations · Full text

Systems Biology, Mendelian Disorder, Complicated Forms +7

Variants in KIF1A gene in dominant and sporadic forms of hereditary spastic paraparesis

Andrea Citterio, Alessia Arnoldi, Elena Panzeri et al. · Journal of Neurology · 2015 · 67 citations · Full text

Genetic Disorder, Kif1a Gene, Genetics +6