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Neurology|December 19, 2022
Genetic Causes of Cerebral Small Vessel Diseases: A Practical Guide for NeurologistsArianna Manini, Leonardo Pantoni
Molecular Neurobiology|January 19, 2021
CADASIL from Bench to Bedside: Disease Models and Novel Therapeutic ApproachesArianna Manini, Leonardo Pantoni
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 4, 2022
Rapidly progressive dementia and intractable diarrhea: a teaching case report and a systematic review of cognitive impairment in Whipple's diseaseArianna Manini, Giacomo Querzola, Carlo Lovati, et al.
Cellular and Molecular Life Sciences : CMLS|June 21, 2022
Inhibition of myostatin and related signaling pathways for the treatment of muscle atrophy in motor neuron diseasesElena Abati, Arianna Manini, Giacomo Pietro Comi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 14, 2021
The impact of lockdown during SARS-CoV-2 outbreak on behavioral and psychological symptoms of dementiaArianna Manini, Michela Brambilla, Laura Maggiore, et al.
Ageing Research Reviews|February 3, 2022
Mitochondrial DNA homeostasis impairment and dopaminergic dysfunction: A trembling balanceArianna Manini, Elena Abati, Giacomo Pietro Comi, et al.
Frontiers in Neurology|January 31, 2022
Adeno-Associated Virus (AAV)-Mediated Gene Therapy for Duchenne Muscular Dystrophy: The Issue of Transgene PersistenceArianna Manini, Elena Abati, Andi Nuredini, et al.
Annals of Medicine|August 24, 2022
A cross-sectional survey study of the impact of COVID-19 pandemic on the training and quality of life of Italian medical residents in the Lombardy regionElena Abati, Leonardo Nelva Stellio, Arianna Manini, et al.
Neurology. Genetics|July 11, 2022
Expanding the Phenotypic Spectrum of Vocal Cord and Pharyngeal Weakness With Distal Myopathy due to the p.S85C MATR3 MutationArianna Manini, Daniele Velardo, Patrizia Ciscato, et al.
Frontiers in Neurology|March 14, 2022
Case Report: Thymidine Kinase 2 (TK2) Deficiency: A Novel Mutation Associated With Childhood-Onset Mitochondrial Myopathy and Atypical ProgressionArianna Manini, Megi Meneri, Carmelo Rodolico, et al.
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