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Annals of Clinical and Translational Neurology|June 27, 2025
Detecting rs-fMRI Networks in Disorders of Consciousness: Improving Clinical InterpretabilityJean Paul Medina Carrion, Mario Stanziano, Ludovico D'Incerti, et al.
Brain Communications|January 12, 2026
PET in conjunction with resting-state functional MRI for the study of chronic disorders of consciousnessAlice Deruti, Jean P Medina Carrion, Mario Stanziano, et al.
Neurobiology of Disease|April 8, 2026
Longitudinal and combined assessment of 24(S)-hydroxycholesterol and Neurofilament light chain in the early stages of Huntington's diseaseLidia Sarro, Marta Valenza, Alessia Mongelli, et al.
International Journal of Molecular Sciences|November 23, 2018
Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya SyndromeSciacca Francesca Luisa, Ambra Rizzo, Gloria Bedini, et al.
Annals of Clinical and Translational Neurology|January 18, 2024
Resting-state fMRI functional connectome of C9orf72 mutation statusMario Stanziano, Davide Fedeli, Umberto Manera, et al.
International Journal of Molecular Sciences|December 22, 2019
Correction: Sciacca, F. L., et al. Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome. Int. J. Mol. Sci. 2018, 19, 3675Francesca Luisa Sciacca, Ambra Rizzo, Gloria Bedini, et al.
Acta Neuropathologica Communications|January 5, 2019
Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein geneGiuseppe Di Fede, Marcella Catania, Cristiana Atzori, et al.
Neuroimage|July 28, 2009
Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6Jörg B Schulz, Johannes Borkert, Stefanie Wolf, et al.
Brain : a Journal of Neurology|February 21, 2013
Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6Kathrin Reetz, Ana S Costa, Shahram Mirzazade, et al.
European Journal of Neurology|March 12, 2024
Distinct neural signatures of pulvinar in C9orf72 amyotrophic lateral sclerosis mutation carriers and noncarriersAnna Nigri, Mario Stanziano, Davide Fedeli, et al.
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