Arianna Manini
5PUBLICATIONS
14CO-AUTHORS
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Publications (5)
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|Aug 22, 2025
Whole genome sequencing analysis in primary lateral sclerosis (PLS) patients reveals mutations in neurological diseases-causing genes.Arianna Manini, Alberto Brusati, Maurizio Grassano
|Apr 25, 2025
KIF5A p.Pro986Leu Risk Variant and Accelerated Progression of Amyotrophic Lateral Sclerosis.Arianna Manini, Rosario Vasta, Alberto Brusati
|Dec 19, 2022
Genetic Causes of Cerebral Small Vessel Diseases: A Practical Guide for Neurologists.Arianna Manini, Leonardo Pantoni
|Sep 13, 2022
Etiologic reclassification of cryptogenic stroke after implantable cardiac monitoring and computed tomography angiography re-assessment.Francesco Mele, Giuseppe Scopelliti, Arianna Manini
|Jul 11, 2022
Expanding the Phenotypic Spectrum of Vocal Cord and Pharyngeal Weakness With Distal Myopathy due to the p.S85C MATR3 Mutation.Arianna Manini, Daniele Velardo, Patrizia Ciscato
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Frequent Collaborators
2 joint publications
Leonardo Pantoni
2 joint publications
Nicola Ticozzi
2 joint publications
Vincenzo Silani
1 joint publications
Daniele Velardo
1 joint publications
Dario Ronchi
1 joint publications
Francesco Mele
1 joint publications
Giuseppe Scopelliti
1 joint publications
Rosario Vasta
1 joint publications
Alessio Maranzano
1 joint publications
Antonio Canosa
