G. Lauria Pinter

Neutralizing antibodies to Omicron after the fourth SARS-CoV-2 mRNA vaccine dose in immunocompromised patients highlight the need of additional boosters

G. Ciliberto, F. Baldanti, G. Apolone, 2022, Frontiers in Immunology.

Analysis of miRNA rare variants in amyotrophic lateral sclerosis and in silico prediction of their biological effects

S. Corti, C. Gellera, N. Ticozzi, 2022, Frontiers in Genetics.

Headache, chest pain, and multiplex cranial neuropathy

F. Ferracci, A. Perin, A. Erbetta, 2019, Neurological Sciences.

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

Ewout J. N. Groen, Annelot M. Dekker, Ross P. Byrne, 2021, Nature Genetics.

DNAJB2‐related Charcot‐Marie‐Tooth disease type 2: Pathomechanism insights and phenotypic spectrum widening

D. Pareyson, F. Taroni, S. Magri, 2022, European journal of neurology.

Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.

F. Marrosu, A. Chiò, G. Mora, 2012, Brain : a journal of neurology.