Impact of age on neurofilament light chain in Friedreich ataxia: a 1-year longitudinal study

Sara Petrillo(Bambino Gesù Children's Hospital), Caterina Mariotti(Fondazione IRCCS Istituto Neurologico Carlo Besta), Lidia Sarro(Fondazione IRCCS Istituto Neurologico Carlo Besta), Barbara Castellotti(Fondazione IRCCS Istituto Neurologico Carlo Besta), Riccardo Ronco(Fondazione IRCCS Istituto Neurologico Carlo Besta), Cinzia Gellera(Fondazione IRCCS Istituto Neurologico Carlo Besta), Alessia Mongelli(Fondazione IRCCS Istituto Neurologico Carlo Besta), Fiorella Piemonte(Institute for Neurodegenerative Disorders), Samuele Azzarelli(Istituto Nazionale di Fisica Nucleare, Sezione di Milano), Anna Castaldo
Brain Communications
January 1, 2025
10.1093/braincomms/fcaf331
Cited by 1

Related Papers

Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis
|Nature|2012|599
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
|Nature Genetics|2021|567
Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS
|Neuron|2014|372
Phenotypic variability in friedreich ataxia: Role of the associated GAA triplet repeat expansion
|Annals of Neurology|1997|271
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
|Nature Genetics|2023|219