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Journal of the Neurological Sciences|April 18, 2025
Characterization of human healthy i<sup>3</sup> lower motor neurons exposed to CSF from ALS patients stratified by UNC13A and C9ORF72 genotypeValeria Casiraghi, Enrico Pellegrini, Alberto Brusati, et al.
Frontiers in Psychology|July 26, 2021
Attachment, Personality and Locus of Control: Psychological Determinants of Risk Perception and Preventive Behaviors for COVID-19Sofia Tagini, Agostino Brugnera, Roberta Ferrucci, et al.
Biomed Research International|September 16, 2017
Brain-Computer Interface for Clinical Purposes: Cognitive Assessment and RehabilitationLaura Carelli, Federica Solca, Andrea Faini, et al.
Brain Sciences|July 27, 2022
Gaze-Contingent Eye-Tracking Training in Brain Disorders: A Systematic ReviewLaura Carelli, Federica Solca, Sofia Tagini, et al.
Frontiers in Endocrinology|December 19, 2022
Emotional and autonomic response to visual erotic stimulation in patients with functional hypothalamic amenorrheaNatale Maiorana, Agostino Brugnera, Valentina Galiano, et al.
Cerebrovascular Diseases (Basel, Switzerland)|June 1, 2023
The Single-Matrix Digit Cancellation Test, a Screener for Selective Attention Deficits: Standardization in an Italian Population Sample and Clinical Usability in Acute Stroke PatientsFabrizio Pasotti, Edoardo Nicolò Aiello, Alessandra Bollani, et al.
Human Molecular Genetics|September 2, 2024
NEK1 haploinsufficiency worsens DNA damage, but not defective ciliogenesis, in C9ORF72 patient-derived iPSC-motoneuronsSerena Santangelo, Sabrina Invernizzi, Marta Nice Sorce, et al.
Biomedicines|May 27, 2023
Identification of Novel Biomarkers of Spinal Muscular Atrophy and Therapeutic Response by Proteomic and Metabolomic Profiling of Human Biological Fluid SamplesMegi Meneri, Elena Abati, Delia Gagliardi, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 15, 2023
Analysis of normal <i>C9orf72</i> repeat length as possible disease modifier in amyotrophic lateral sclerosisSilvia Peverelli, Alberto Brusati, Valeria Casiraghi, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 6, 2022
Expanding the phenotype of <i>TARDBP</i> mutation in a Tunisian family with clinical phenotype heterogeneityImen Kacem, Ikram Sghaier, Nicola Ticozzi, et al.
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