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Scientific Reports|February 24, 2023
NOTCH2NLC GGC repeats are not expanded in Italian amyotrophic lateral sclerosis patientsArianna Manini, Delia Gagliardi, Megi Meneri, et al.
Annals of Clinical and Translational Neurology|October 26, 2022
Analysis of HTT CAG repeat expansion in Italian patients with amyotrophic lateral sclerosisArianna Manini, Delia Gagliardi, Megi Meneri, et al.
Journal of Neurology|September 13, 2022
Etiologic reclassification of cryptogenic stroke after implantable cardiac monitoring and computed tomography angiography re-assessmentFrancesco Mele, Giuseppe Scopelliti, Arianna Manini, et al.
International Journal of Molecular Sciences|August 26, 2022
TMEM106B Acts as a Modifier of Cognitive and Motor Functions in Amyotrophic Lateral SclerosisArianna Manini, Antonia Ratti, Alberto Brusati, et al.
Frontiers in Genetics|June 17, 2022
Case Report: Rare Homozygous RNASEH1 Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA DeletionsArianna Manini, Leonardo Caporali, Megi Meneri, et al.
Parkinsonism & Related Disorders|July 3, 2021
Screening of LRP10 mutations in Parkinson's disease patients from ItalyArianna Manini, Letizia Straniero, Edoardo Monfrini, et al.
Scientific Reports|April 14, 2022
Clinical and genetic features of a cohort of patients with MFN2-related neuropathyElena Abati, Arianna Manini, Daniele Velardo, et al.
BMC Neurology|November 8, 2020
A case report of late-onset cerebellar ataxia associated with a rare p.R342W TGM6 (SCA35) mutationArianna Manini, Tommaso Bocci, Alice Migazzi, et al.
Molecular Genetics and Metabolism Reports|June 27, 2022
A novel RRM2B mutation associated with mitochondrial DNA depletion syndromeMonica Fumagalli, Dario Ronchi, Maria Francesca Bedeschi, et al.
Frontiers in Aging Neuroscience|February 23, 2023
Association of the risk factor UNC13A with survival and upper motor neuron involvement in amyotrophic lateral sclerosisArianna Manini, Valeria Casiraghi, Alberto Brusati, et al.
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