Davide Pareyson

56PUBLICATIONS
202CO-AUTHORS
Neurology and neuromuscular diseasesAutonomic nervous systemImmunogenetics (incl. genetic immunology)Behavioural epidemiologyMedical molecular engineering of nucleic acids and proteins
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Publications (56)

|Jun 10, 2026
Pharmacological Interventions for Hereditary Transthyretin-Related Amyloidosis With Polyneuropathy: Systematic Review and Network Meta-Analysis.

|Jun 05, 2026
A Quantitative Assessment of Upper Limb Motor Function Across Disease Stages in Hereditary Transthyretin Amyloidosis.

|Jun 02, 2026
Deep Phenotyping of F64L Mutation in a Multicentric Cohort of Patisiran-Treated Hereditary Transthyretin Amyloidosis Patients (Patisiranitaly).

|May 06, 2026
Clinical and pathological findings in two Italian siblings of Romani ancestry with charcot-marie-tooth type 4D and review of the current literature.

|Feb 14, 2026
Mitochondrial energetic failure underlies FLVCR1-related sensory neuropathy.

Francesca Bertino, Diletta Isabella Zanin Venturini, Eleonora Grasso

|Feb 10, 2026
Adrenoleukodystrophy in adults: phenotypic characterisation and natural history in a large cohort.

Chiara Benzoni, Marco Moscatelli, Paola Lanteri

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Frequent Collaborators

20 joint publications

Chiara Pisciotta

10 joint publications

Michael E Shy

9 joint publications

Stefano Tozza

8 joint publications

Stefano Carlo Previtali