Fabrizio Tagliavini


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Person Info

NAME

Fabrizio

SURNAME

Tagliavini

Publications in SciGraph latest 50 shown

  • 2019-12 Clinical and neuropathological phenotype associated with the novel V189I mutation in the prion protein gene in ACTA NEUROPATHOLOGICA COMMUNICATIONS
  • 2018-12 Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference in NATURE COMMUNICATIONS
  • 2018-12 Distinct patterns of brain atrophy in Genetic Frontotemporal Dementia Initiative (GENFI) cohort revealed by visual rating scales in ALZHEIMER'S RESEARCH & THERAPY
  • 2018-12 Molecular subtypes of Alzheimer’s disease in SCIENTIFIC REPORTS
  • 2018-12 Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study in ACTA NEUROPATHOLOGICA COMMUNICATIONS
  • 2018-08-03 Synthetic Prion Selection and Adaptation in MOLECULAR NEUROBIOLOGY
  • 2018-08 In Situ Tissue Labeling of Cerebral Amyloid Using HIV-Related Tat Peptide in MOLECULAR NEUROBIOLOGY
  • 2018-06 Combining drug and music therapy in patients with moderate Alzheimer’s disease: a randomized study in NEUROLOGICAL SCIENCES
  • 2018-04 An In Vivo 11C-(R)-PK11195 PET and In Vitro Pathology Study of Microglia Activation in Creutzfeldt-Jakob Disease in MOLECULAR NEUROBIOLOGY
  • 2017-12 Differential overexpression of SERPINA3 in human prion diseases in SCIENTIFIC REPORTS
  • 2017-12 Detection of prion seeding activity in the olfactory mucosa of patients with Fatal Familial Insomnia in SCIENTIFIC REPORTS
  • 2017-12 The A2V mutation as a new tool for hindering Aβ aggregation: A neutron and x-ray diffraction study in SCIENTIFIC REPORTS
  • 2017-12 α-Synuclein Amyloids Hijack Prion Protein to Gain Cell Entry, Facilitate Cell-to-Cell Spreading and Block Prion Replication in SCIENTIFIC REPORTS
  • 2016-08 Tackling amyloidogenesis in Alzheimer’s disease with A2V variants of Amyloid-β in SCIENTIFIC REPORTS
  • 2016-03 MRI abnormalities found 1 year prior to symptom onset in a case of Creutzfeldt–Jakob disease in JOURNAL OF NEUROLOGY
  • 2016-01 Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy in ACTA NEUROPATHOLOGICA
  • 2015-05 Italian Frontotemporal Dementia Network (FTD Group-SINDEM): sharing clinical and diagnostic procedures in Frontotemporal Dementia in Italy in NEUROLOGICAL SCIENCES
  • 2015 Prion Diseases in PROGNOSIS OF NEUROLOGICAL DISEASES
  • 2014-12 Defined α-synuclein prion-like molecular assemblies spreading in cell culture in BMC NEUROSCIENCE
  • 2014-07 Idiopathic progressive chorea: misnomer or still reality? A case with neuropathological disconfirmation in NEUROLOGICAL SCIENCES
  • 2014-03 Mutations in MAPT give rise to aneuploidy in animal models of tauopathy in NEUROGENETICS
  • 2013-07 Prion disease: A promising rating scale for prion disease clinical research in NATURE REVIEWS NEUROLOGY
  • 2013-03 Erratum to: APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38 in ACTA NEUROPATHOLOGICA
  • 2012-12 APP mutations in the Aβ coding region are associated with abundant cerebral deposition of Aβ38 in ACTA NEUROPATHOLOGICA
  • 2012-11 Stereotypic behaviors in degenerative dementias in JOURNAL OF NEUROLOGY
  • 2012-10 Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA in ACTA NEUROPATHOLOGICA
  • 2012-06 Lewy body pathology and typical Parkinson disease in a patient with a heterozygous (R275W) mutation in the Parkin gene (PARK2) in ACTA NEUROPATHOLOGICA
  • 2012-02 A progranulin mutation associated with cortico-basal syndrome in an Italian family expressing different phenotypes of fronto-temporal lobar degeneration in NEUROLOGICAL SCIENCES
  • 2012-02 Position paper of the Italian Society for the study of Dementias (Sindem) on the proposal of a new Lexicon on Alzheimer disease in NEUROLOGICAL SCIENCES
  • 2010-12 Neuropathology of the recessive A673V APP mutation: Alzheimer disease with distinctive features in ACTA NEUROPATHOLOGICA
  • 2009-10 Creutzfeldt–Jakob disease with E200K PRNP mutation: a case report and revision of the literature in NEUROLOGICAL SCIENCES
  • 2009-10 Regression of chronic posterior leukoencephalopathy after stop of methotrexate treatment in NEUROLOGICAL SCIENCES
  • 2008-12 Atypical frontotemporal dementia as a new clinical phenotype of Gerstmann-Straussler-Scheinker disease with the PrP-P102L mutation. Description of a previously unreported Italian family in NEUROLOGICAL SCIENCES
  • 2008-10 The anti-fibrillogenic activity of tetracyclines on PrP 106–126: a 3D-QSAR study in JOURNAL OF MOLECULAR MODELING
  • 2007-08 Poster abstracts in SLEEP AND BIOLOGICAL RHYTHMS
  • 2005-12 Familial frontotemporal dementia associated with the novel MAPT mutation T427M in JOURNAL OF NEUROLOGY
  • 2005-09 Redox metals and oxidative abnormalities in human prion diseases in ACTA NEUROPATHOLOGICA
  • 2005 Hereditary Prion Protein Amyloidoses in NEURODEGENERATION AND PRION DISEASE
  • 2004 Cytotoxicity of PrP Peptides in TECHNIQUES IN PRION RESEARCH
  • 2003-02 Amyloid β plaque-associated proteins C1q and SAP enhance the Aβ1–42 peptide-induced cytokine secretion by adult human microglia in vitro in ACTA NEUROPATHOLOGICA
  • 1998 PrP Peptides as a Tool to Investigate the Pathogenesis of Prion Protein Amyloidoses in PRIONS AND BRAIN DISEASES IN ANIMALS AND HUMANS
  • 1998 Clinical, Pathological, and Molecular Characterization of Gerstmann-Sträussler-Scheinker Disease in the Indiana Kindred (PRNP F198S) in PRIONS AND BRAIN DISEASES IN ANIMALS AND HUMANS
  • 1998 Anthracyclines and Amyloidosis in PROGRESS IN ALZHEIMER’S AND PARKINSON’S DISEASES
  • 1996-05 Apoptosis-mediated neurotoxicity induced by β-amyloid and PRP fragments in JOURNAL OF MOLECULAR NEUROSCIENCE
  • 1996-04-17 Methods for Studying Prion Protein in PRION DISEASES
  • 1995-04 Tau protein directly interacts with the amyloid β-protein precursor: Implications for Alzheimer's disease in NATURE MEDICINE
  • 1994-02 Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles in MOLECULAR NEUROBIOLOGY
  • 1993-04 Neurotoxicity of a prion protein fragment in NATURE
  • 1993-02 Ubiquitinated neurites are associated with preamyloid and cerebral amyloid β deposits in patients with hereditary cerebral hemorrhage with amyloidosis Dutch type in ACTA NEUROPATHOLOGICA
  • 1988-01 Progressive supranuclear palsy with hypertrophy of the olives in ACTA NEUROPATHOLOGICA
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