Silvia Paverelli (S Peverelli, Silvia Peverelli)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 6

Top Topics

Amyotrophic Lateral Sclerosis

Gene Expression

Parkinson Disease

Top Venues

Amyotrophic lateral sclerosis & frontotemporal degeneration

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Silvia Paverelli, Alberto Brusati, Valeria Casiraghi, Marta Nice Sorce, Sabrina Invernizzi, Serena Santangelo, Claudia Morelli, Federico Verde, Vincenzo Silani, Nicola Ticozzi, Antonia Ratti
Analysis of normal C9orf72 repeat length as possible disease modifier in amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis & frontotemporal degeneration 25 (1-2) (2024)
Silvia Paverelli, Alberto Brusati, Valeria Casiraghi, Marta Nice Sorce, Sabrina Invernizzi, Serena Santangelo, Claudia Morelli, Federico Verde, Vincenzo Silani, Nicola Ticozzi, Antonia Ratti
Analysis of normal C9orf72 repeat length as possible disease modifier in amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis & frontotemporal degeneration 25 (1-2) (2024)
I Kacem, I Sghaier, Silvia Paverelli, Y Abida, H Ben Brahim, A Ratti, A Nasri, Nicola Ticozzi, Vincenzo Silani, Riadh Goudier
Optineurin in patients with Amyotrophic Lateral Sclerosis associated to atypical Parkinsonism in Tunisian population. Amyotrophic lateral sclerosis & frontotemporal degeneration (2023)
Silvia Paverelli, Alberto Brusati, Valeria Casiraghi, Marta Nice Sorce, Sabrina Invernizzi, Serena Santangelo, Claudia Morelli, Federico Verde, Vincenzo Silani, Nicola Ticozzi, Antonia Ratti
Analysis of normal C9orf72 repeat length as possible disease modifier in amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis & frontotemporal degeneration (2023)
Ikram Sghaier, Imen Kacem, Nicola Ticozzi, Saloua Mrabet, Silvia Paverelli, Youssef Abida, Antonia Ratti, Vincenzo Silani, Riadh Goudier
The oligogenic model of amyotrophic lateral sclerosis; phenotypes of three Tunisian families. Clinical genetics 102 (6) (2022)
Antonia Ratti, Silvia Paverelli, Elisabetta D'Adda, Claudia Colombrita, Michele Gennuso, Alessandro Prelle, Vincenzo Silani
Genetic and epigenetic disease modifiers in an Italian C9orf72 family expressing ALS, FTD or PD clinical phenotypes. Amyotrophic lateral sclerosis & frontotemporal degeneration (2021)