Sabina Capellari
Affiliations: | Università di Bologna, Bologna, Italy |
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| 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 |
| Abu-Rumeileh S, Barschke P, Oeckl P, et al. (2022) Prodynorphin and Proenkephalin in Cerebrospinal Fluid of Sporadic Creutzfeldt-Jakob Disease. International Journal of Molecular Sciences. 23 |