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Alessia Arnoldi

Observed names: A Arnoldi, A. Arnoldi, Arnoldi, Alessia
Institution: IRCCS Eugenio Medea
OpenAlex ID: A5000715305
Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot–Marie–Tooth type 2
2011 · C Crimella, C Baschirotto, et al. · Clinical Genetics · 162
Hereditary spastic paraplegia type 5: natural history, biomarkers and a randomized controlled trial
2017 · Ludger Schöls, Tim W Rattay, et al. · Brain · 116
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A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegia
2008 · Alessia Arnoldi, Alessandra Tonelli, et al. · Human Mutation · 103
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Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis
2013 · Andrea Citterio, Alessia Arnoldi, et al. · Journal of Neurology · 81
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Variants in KIF1A gene in dominant and sporadic forms of hereditary spastic paraparesis
2015 · Andrea Citterio, Alessia Arnoldi, et al. · Journal of Neurology · 66
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ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis
2018 · Chiara Vantaggiato, Elena Panzeri, et al. · Autophagy · 60
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Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot Study
2016 · Andrea Martinuzzi, Domenico Montanaro, et al. · PLoS ONE · 48
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Eight Novel Mutations in SPG4 in a Large Sample of Patients With Hereditary Spastic Paraplegia
2006 · Francesca Crippa, Chris Panzeri, et al. · Archives of Neurology · 48
Genetic features of antidepressant induced mania and hypo-mania in bipolar disorder
2004 · Alessandro Serretti, Paola Artioli, et al. · Psychopharmacology · 47
Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutations
2011 · A Arnoldi, C Crimella, et al. · Clinical Genetics · 45
Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum
2009 · C Crimella, A Arnoldi, et al. · Journal of Medical Genetics · 33
Impairment of brain and muscle energy metabolism detected by magnetic resonance spectroscopy in hereditary spastic paraparesis type 28 patients with DDHD1 mutations
2014 · Rocco Liguori, Maria Pia Giannoccaro, et al. · Journal of Neurology · 30
Hereditary spastic paraparesis in adults. A clinical and genetic perspective from Tuscany
2014 · Daniele Orsucci, Loredana Petrucci, et al. · Clinical Neurology and Neurosurgery · 29
Atypical adult onset complicated spastic paraparesis with thin corpus callosum in two patients carrying a novel FA2H mutation
2012 · A. Tonelli, M. G. D'Angelo, et al. · European Journal of Neurology · 25
A Novel Mutation in Motor Domain of KIF5A Associated With an HSP/Axonal Neuropathy Phenotype
2015 · Fabrizio Rinaldi, Maria T. Bassi, et al. · Journal of Clinical Neuromuscular Disease · 17
Atypical late-onset hereditary spastic paraplegia with thin corpus callosum due to novel compound heterozygous mutations in the SPG11 gene
2014 · Maria Pia Giannoccaro, Rocco Liguori, et al. · Journal of Neurology · 17
The blurred scenario of motor neuron disorders linked to S patacsin mutations: a case report
2014 · G. Querin, C. Bertolin, et al. · European Journal of Neurology · 3
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Works count: 18
Citation count: 930
H-index: 16
I10-index: 16
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