Alessia Arnoldi

Bosisio Parini, Italy

Last Updated: 09/26/2026

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Found 11 publications

ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis.

ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis.

Journal: Autophagy

Published: August 08, 2018

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

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

Journal: Brain : a journal of neurology

Published: May 02, 2017

Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot Study.

Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot Study.

Journal: PloS one

Published: October 08, 2015

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

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

Journal: Journal of neurology

Published: July 02, 2015

A novel mutation in motor domain of KIF5A associated with an HSP/axonal neuropathy phenotype.

A novel mutation in motor domain of KIF5A associated with an HSP/axonal neuropathy phenotype.

Journal: Journal of clinical neuromuscular disease

Published: February 20, 2015

Atypical late-onset hereditary spastic paraplegia with thin corpus callosum due to novel compound heterozygous mutations in the SPG11 gene.

Atypical late-onset hereditary spastic paraplegia with thin corpus callosum due to novel compound heterozygous mutations in the SPG11 gene.

Journal: Journal of neurology

Published: June 19, 2014

Impairment of brain and muscle energy metabolism detected by magnetic resonance spectroscopy in hereditary spastic paraparesis type 28 patients with DDHD1 mutations.

Impairment of brain and muscle energy metabolism detected by magnetic resonance spectroscopy in hereditary spastic paraparesis type 28 patients with DDHD1 mutations.

Journal: Journal of neurology

Published: May 02, 2014

The blurred scenario of motor neuron disorders linked to Spatacsin mutations: a case report.

The blurred scenario of motor neuron disorders linked to Spatacsin mutations: a case report.

Journal: European journal of neurology

Published: January 29, 2014

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

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

Journal: Journal of neurology

Published: October 31, 2013

Hereditary spastic paraparesis in adults. A clinical and genetic perspective from Tuscany.

Hereditary spastic paraparesis in adults. A clinical and genetic perspective from Tuscany.

Journal: Clinical neurology and neurosurgery

Published: April 20, 2013

Atypical adult onset complicated spastic paraparesis with thin corpus callosum in two patients carrying a novel FA2H mutation.

Atypical adult onset complicated spastic paraparesis with thin corpus callosum in two patients carrying a novel FA2H mutation.

Journal: European journal of neurology

Published: May 07, 2012

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Last Updated: 09/26/2026