Get started
Author

Sara Locci

Observed name: Locci, Sara
Institution: University of Siena
OpenAlex ID: A5059540491
Vitamin D in Neurological Diseases
2022 · Domenico Plantone, Guido Primiano, et al. · International Journal of Molecular Sciences · 72
Brain neuronal and glial damage during acute COVID-19 infection in absence of clinical neurological manifestations
2022 · Domenico Plantone, Sara Locci, et al. · Journal of Neurology Neurosurgery & Psychiatry · 27
Neurofilament light chain and glial fibrillary acid protein levels are elevated in post-mild COVID-19 or asymptomatic SARS-CoV-2 cases
2024 · Domenico Plantone, Angela Stufano, et al. · Scientific Reports · 19
PDF
B Lymphocytes in Alzheimer’s Disease—A Comprehensive Review
2022 · Domenico Plantone, Matteo Pardini, et al. · Journal of Alzheimer s Disease · 17
Gordon Holmes syndrome caused by two novel mutations in the PNPLA6 gene
2021 · Sara Locci, Silvia Bianchi, et al. · Clinical Neurology and Neurosurgery · 14
Familial Alzheimer’s disease associated with heterozygous NPC1 mutation
2023 · Diego Lopergolo, Silvia Bianchi, et al. · Journal of Medical Genetics · 12
A Systematic Review Focusing on the Link between Engineered Nanoparticles and Neurodegeneration
2025 · Carlo Manco, Delia Righi, et al. · ACS Chemical Neuroscience · 11
Clinically relevant increases in serum neurofilament light chain and glial fibrillary acidic protein in patients with Susac syndrome
2023 · Domenico Plantone, Eleonora Sabatelli, et al. · European Journal of Neurology · 6
24S-Hydroxycholesterol and Cerebellar Degeneration: Insights from SCA2
2022 · Sara Locci, Valentina Nidiaci, et al. · The Cerebellum · 4
Co-occurrence of DMPK expansion and CLCN1 mutation in a patient with myotonia
2021 · Sara Locci, Rosanna Cardani, et al. · Neurological Sciences · 4
Serum growth differentiation factor-15, glial fibrillary acidic protein, and neurofilament light chain: Their link and role in Creutzfeldt-Jakob disease
2024 · Carlo Manco, Domenico Plantone, et al. · Journal of the Neurological Sciences · 2
PDF
Primary familial brain calcification with mild phenotype due to a new PDGFB mutation
2022 · Sara Locci, Silvia Bianchi, et al. · Neurological Sciences · 1
Serum neuronal, glial and mitochondrial markers in autosomal dominant optic atrophy and Leber hereditary optic neuropathy
2025 · Alessandra Rufa, Domenico Plantone, et al. · Brain Communications
PDF
Works count: 14
Citation count: 189
H-index: 7
I10-index: 7
Year
Topic
Type