sabina capellari
University of Bologna
Research areas: Medicine · Internal Medicine · Prion Diseases and Protein Misfolding · Alzheimer's disease research and treatments · Amyloidosis: Diagnosis, Treatment, Outcomes
0000-0003-1631-1439
About
EDUCATION:
- 1991, M.D., University of Bologna, Italy
- 1995, Neurology, University of Bologna, Italy.
PROFESSIONAL EXPERIENCE
- 1995-1999, Research associate, Division of Neuropathology of the Case Western Reserve University, Cleveland, Ohio, USA.
- 1997-1999, In charge of the genetic analysis for the TSE surveillance of United States directed by Prof. Pierluigi Gambetti.
- 2000-2005, PostDoc at the Department of Neurological Sciences of the University of Bologna.
- April 2005-: Assistant Professor at the Department of Neurological Sciences of the University of Bologna.
- 2010-: Neurologist at IRCCS ISNB, Ospedale Bellaria, Bologna.
- 2021-: Associate Professor, Department of Biomedical and Neuromotor Science, University of Bologna
Since 2008 Teaching activity for the Medical School, Neurology Residency Program.
SCIENTIFIC ACTIVITY
Fields of interest: Neurology and Neurogenetics. Human prion diseases, Movement Disorders, Dementia. Genetic of neurodegenerative diseases.
Financial support by Italian Ministry of Health. Participant in European Projects, Telethon Project, Network of Excellence of the EC.
Employment
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University of Bologna Associate Professor2021 - Present
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University of Bologna and IRCCS Istituto delle Scienze Neurologiche di Bologna Assistant Professor and Neurologist2005 - Present
Education
Education history is unavailable.
Projects & Funding
Projects & funding information is unavailable.
Publications (186)
- AKiD_Official_Research_Protocol Save
- AKiDproject--formants_F1F2F3_cardinalVowels_readingTask Save
- CSF1R mutations in an Italian population of early-onset dementia: a case series Save
- Pharmacotherapy for behavioural manifestations in frontotemporal dementia: An expert consensus from the European Reference Network for Rare Neurological Diseases (ERN‐RND) Save
- “Build Your Village”—Conducting the Village Test on Cognitively Impaired Patients: A First Journey into Alzheimerland Save
- Diagnostic and Prognostic Value of Plasma GFAP in Sporadic Creutzfeldt–Jakob Disease in the Clinical Setting of Rapidly Progressive Dementia Save
- Rapidly progressive dementia due to intravascular lymphoma: A prion disease reference center experience Save
- Amyloid-Beta Co-Pathology Is a Major Determinant of the Elevated Plasma GFAP Values in Amyotrophic Lateral Sclerosis Save
- Defining the phenotypic spectrum of sporadic Creutzfeldt–Jakob disease MV2K: the kuru plaque type Save
- The Genetic Puzzle of a SOD1-Patient with Ocular Ptosis and a Motor Neuron Disease: How Many Variants Contribute to the Phenotype? Save
- Frequency of Parkinson’s Disease Genes and Role of PARK2 in Amyotrophic Lateral Sclerosis: An NGS Study Save
- Antibodies to neuronal surface antigens in patients with a clinical diagnosis of neurodegenerative disorder Save
- In Vivo Diagnosis of Synucleinopathies Save
- Anterior Callosal Angle: A New Marker of Idiopathic Normal Pressure Hydrocephalus? Save
- CSF SerpinA1 in Creutzfeldt–Jakob disease and frontotemporal lobar degeneration Save
- Characterization of novel progranulin gene variants in Italian patients with neurodegenerative diseases Save
- Csf ubiquitin levels are higher in alzheimer’s disease than in frontotemporal dementia and reflect the molecular subtype in prion disease Save
- Detection of prions in skin punch biopsies of Creutzfeldt–Jakob disease patients Save
- First case of an UBQLN2 gene mutation causing frontotemporal dementia preceded by adult onset psychiatric symptoms Save
- Spatial Epidemiology of Sporadic Creutzfeldt-Jakob Disease in Apulia, Italy Save