Get started
Author

Anna Bartoletti‐Stella

Observed names: A Bartoletti-Stella, A. Bartoletti-Stella, Anna Bartoletti Stella, Anna Bartoletti-Stella, Bartoletti AS, Bartoletti-Stella, A., Bartoletti-Stella, Anna
Observed institutions: Copenhagen University Hospital, Rigshospitalet, Istituto delle Scienze Neurologiche di Bologna, Ospedale Bellaria, University of Florence, University of Bologna
ORCID: 0000-0001-6442-162X
Observed ORCID: 0000-0001-6442-162X
OpenAlex ID: A5045138201
CSF biomarkers of neuroinflammation in distinct forms and subtypes of neurodegenerative dementia
2019 · Samir Abu-Rumeileh, Petra Steinacker, et al. · Alzheimer s Research & Therapy · 154
PDF
The genetic and metabolic signature of oncocytic transformation implicates HIF1α destabilization
2009 · Anna Maria Porcelli, Anna Ghelli, et al. · Human Molecular Genetics · 121
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study
2020 · Emma Jones, Holger Hummerich, et al. · The Lancet Neurology · 78
PDF
Cerebrospinal Fluid Biomarkers in Patients with Frontotemporal Dementia Spectrum: A Single-Center Study
2018 · Samir Abu-Rumeileh, Nicola Mometto, et al. · Journal of Alzheimer s Disease · 65
Comparison between plasma and cerebrospinal fluid biomarkers for the early diagnosis and association with survival in prion disease
2020 · Samir Abu-Rumeileh, Simone Baiardi, et al. · Journal of Neurology Neurosurgery & Psychiatry · 55
Gamma rays induce a p53-independent mitochondrial biogenesis that is counter-regulated by HIF1α
2013 · A Bartoletti-Stella, E Mariani, et al. · Cell Death and Disease · 51
PDF
Antemortem CSF A β 42/A β 40 ratio predicts Alzheimer's disease pathology better than A β 42 in rapidly progressive dementias
2018 · Simone Baiardi, Samir Abu‐Rumeileh, et al. · Annals of Clinical and Translational Neurology · 50
PDF
Three-Dimensional Virtual Anatomy as a New Approach for Medical Student’s Learning
2021 · Anna Bartoletti-Stella, Valentina Gatta, et al. · International Journal of Environmental Research and Public Health · 45
PDF
A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype
2014 · Pamela Magini, Tommaso Pippucci, et al. · Human Molecular Genetics · 44
Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature
2017 · Maria Pia Giannoccaro, Anna Bartoletti-Stella, et al. · Journal of Neurology · 37
Early downregulation of hsa-miR-144-3p in serum from drug-naïve Parkinson’s disease patients
2022 · Elisa Zago, Alessandra Dal Molin, et al. · Scientific Reports · 31
Messenger RNA processing is altered in autosomal dominant leukodystrophy
2015 · A. Bartoletti-Stella, L. Gasparini, et al. · Human Molecular Genetics · 31
PDF
Metabolite and lipoprotein profiles reveal sex-related oxidative stress imbalance in de novo drug-naive Parkinson’s disease patients
2022 · Gaia Meoni, Leonardo Tenori, et al. · npj Parkinson s Disease · 30
Extra Virgin Olive Oil (EVOO), a Mediterranean Diet Component, in the Management of Muscle Mass and Function Preservation
2022 · Sara Salucci, Anna Bartoletti-Stella, et al. · Nutrients · 29
PDF
Analysis of RNA Expression Profiles Identifies Dysregulated Vesicle Trafficking Pathways in Creutzfeldt-Jakob Disease
2018 · Anna Bartoletti-Stella, Patrizia Corrado, et al. · Molecular Neurobiology · 24
PDF
Identification of rare genetic variants in Italian patients with dementia by targeted gene sequencing
2018 · Anna Bartoletti-Stella, Simone Baiardi, et al. · Neurobiology of Aging · 23
Cell signaling pathways in autosomal-dominant leukodystrophy (ADLD): the intriguing role of the astrocytes
2020 · Stefano Ratti, Isabella Rusciano, et al. · Cellular and Molecular Life Sciences · 22
PDF
The characterization of AD/PART co-pathology in CJD suggests independent pathogenic mechanisms and no cross-seeding between misfolded Aβ and prion proteins
2019 · Marcello Rossi, Hideaki Kai, et al. · Acta Neuropathologica Communications · 22
PDF
Two novel PRNP truncating mutations broaden the spectrum of prion amyloidosis
2018 · Sabina Capellari, Simone Baiardi, et al. · Annals of Clinical and Translational Neurology · 21
PDF
Targeted sequencing panels in Italian ALS patients support different etiologies in the ALS/FTD continuum
2021 · Anna Bartoletti-Stella, Veria Vacchiano, et al. · Journal of Neurology · 20
PDF
Mitochondrial DNA Mutations in Oncocytic Adnexal Lacrimal Glands of the Conjunctiva
2011 · Anna Bartoletti-Stella · Archives of Ophthalmology · 19
Age at onset of genetic (E200K) and sporadic Creutzfeldt-Jakob diseases is modulated by the CYP4X1 gene
2018 · Anna Poleggi, Sven van der Lee, et al. · Journal of Neurology Neurosurgery & Psychiatry · 18
Phospholipase Family Enzymes in Lung Cancer: Looking for Novel Therapeutic Approaches
2023 · Sara Salucci, Beatrice Aramini, et al. · Cancers · 15
PDF
A geroscience approach for Parkinson’s disease: Conceptual framework and design of PROPAG-AGEING project
2020 · Chiara Pirazzini, Tiago Azevedo, et al. · Mechanisms of Ageing and Development · 15
PDF
A Novel Eight Octapeptide Repeat Insertion in PRNP Causing Prion Disease in a Danish Family
2019 · Aušrinė Areškevičiūtė, Peter Høgh, et al. · Journal of Neuropathology & Experimental Neurology · 15
Works count: 63
Citation count: 1,192
H-index: 20
I10-index: 32
Year
Topic
Type