Roberto Rumore

Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4

G. Rizzo, C. Cereda, A. Filla, 2022, Neurology: Genetics.

RADX Gene Variant May Predispose to Familial Asperger Syndrome

I. Bottillo, F. Gurrieri, E. Tabolacci, 2023, Genes.

A novel AIFM1 missense mutation in a Japanese patient with ataxic sensory neuronopathy and hearing impairment

C. Caltagirone, I. Nishino, T. Kawarai, 2019, Journal of the Neurological Sciences.

Identification of new candidate genes for spina bifida through exome sequencing

F. Gurrieri, E. Ausili, C. Rendeli, 2021, Child's Nervous System.

Identification by Exome Sequencing of Predisposing Variants in Familial Cases of Autoinflammatory Recurrent Fevers

R. Manna, F. Gurrieri, E. Verrecchia, 2023, Genes.