: Rare neurological diseases as a whole share peculiar features as motor and/or cognitive impairment, an elevated disability burden, a frequently chronic course and, in present times, scarcity of therapeutic options. The rarity of those conditions hampers both the identification of significant prognostic outcome measures, and the development of novel therapeutic approaches and clinical trials. Collection of objective clinical data through digital devices can support diagnosis, care, and therapeutic research. We provide an overview on recent developments in the field of digital tools applied to rare neurological diseases, both in the care setting and as providers of outcome measures in clinical trials in a representative subgroup of conditions, including ataxias, hereditary spastic paraplegias, motoneuron diseases and myopathies.

The use of digital tools in rare neurological diseases towards a new care model: a narrative review

Torri, Francesca;Vadi, Gabriele;Meli, Adriana;Loprieno, Sara;Schirinzi, Erika;Lopriore, Piervito;Ricci, Giulia;Siciliano, Gabriele;Mancuso, Michelangelo
2024-01-01

Abstract

: Rare neurological diseases as a whole share peculiar features as motor and/or cognitive impairment, an elevated disability burden, a frequently chronic course and, in present times, scarcity of therapeutic options. The rarity of those conditions hampers both the identification of significant prognostic outcome measures, and the development of novel therapeutic approaches and clinical trials. Collection of objective clinical data through digital devices can support diagnosis, care, and therapeutic research. We provide an overview on recent developments in the field of digital tools applied to rare neurological diseases, both in the care setting and as providers of outcome measures in clinical trials in a representative subgroup of conditions, including ataxias, hereditary spastic paraplegias, motoneuron diseases and myopathies.
2024
Torri, Francesca; Vadi, Gabriele; Meli, Adriana; Loprieno, Sara; Schirinzi, Erika; Lopriore, Piervito; Ricci, Giulia; Siciliano, Gabriele; Mancuso, Mi...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/1245307
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