You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.
Abu-Rumeileh S, Halbgebauer S, Bentivenga GM, et al. (2023) High diagnostic performance of plasma and cerebrospinal fluid beta-synuclein for sporadic Creutzfeldt-Jakob disease. Annals of Clinical and Translational Neurology
Baiardi S, Mammana A, Capellari S, et al. (2023) Human prion disease: molecular pathogenesis, and possible therapeutic targets and strategies. Expert Opinion On Therapeutic Targets. 1-14
Vacchiano V, Mastrangelo A, Zenesini C, et al. (2023) Elevated plasma p-tau181 levels unrelated to Alzheimer's disease pathology in amyotrophic lateral sclerosis. Journal of Neurology, Neurosurgery, and Psychiatry
Baiardi S, Mammana A, Dellavalle S, et al. (2023) Defining the phenotypic spectrum of sporadic Creutzfeldt-Jakob disease MV2K: the kuru plaque type. Brain : a Journal of Neurology
Tarozzi M, Baiardi S, Sala C, et al. (2022) Genomic, transcriptomic and RNA editing analysis of human MM1 and VV2 sporadic Creutzfeldt-Jakob disease. Acta Neuropathologica Communications. 10: 181
Mastrangelo A, Mammana A, Baiardi S, et al. (2022) Evaluation of the impact of CSF prion RT-QuIC and amended criteria on the clinical diagnosis of Creutzfeldt-Jakob disease: a 10-year study in Italy. Journal of Neurology, Neurosurgery, and Psychiatry
Baiardi S, Quadalti C, Mammana A, et al. (2022) Diagnostic value of plasma p-tau181, NfL, and GFAP in a clinical setting cohort of prevalent neurodegenerative dementias. Alzheimer's Research & Therapy. 14: 153
Bartoletti-Stella A, Tarozzi M, Mengozzi G, et al. (2022) Dementia-related genetic variants in an Italian population of early-onset Alzheimer's disease. Frontiers in Aging Neuroscience. 14: 969817
Gelpi E, Baiardi S, Nos C, et al. (2022) Sporadic Creutzfeldt-Jakob disease VM1: phenotypic and molecular characterization of a novel subtype of human prion disease. Acta Neuropathologica Communications. 10: 114
Vacchiano V, Bartoletti-Stella A, Rizzo G, et al. (2022) Frequency of Parkinson's Disease Genes and Role of in Amyotrophic Lateral Sclerosis: An NGS Study. Genes. 13