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List of works by Fabrizio Tagliavini

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A recessive mutation in the APP gene with dominant-negative effect on amyloidogenesis.

scientific article published on March 2009
Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis.

scientific article published on 4 February 2015
Staging of neurofibrillary pathology in Alzheimer's disease: a study of the BrainNet Europe Consortium

scientific article published on 26 March 2008
Sporadic human prion diseases: molecular insights and diagnosis

scientific article published on July 1, 2012
Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy

scientific article published on 10 December 2015
Variably protease-sensitive prionopathy: a new sporadic disease of the prion protein.

scientific article
Frontotemporal dementia and its subtypes: a genome-wide association study

scientific article
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?

scientific article published in March 2007
Pre-symptomatic detection of prions by cyclic amplification of protein misfolding.

scientific article published in January 2005
Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA

scientific article published on 30 June 2012
Prions in the urine of patients with variant Creutzfeldt-Jakob disease

scientific article
Mutant prion protein expression causes motor and memory deficits and abnormal sleep patterns in a transgenic mouse model.

scientific article published in November 2008
Doxycycline in Creutzfeldt-Jakob disease: a phase 2, randomised, double-blind, placebo-controlled trial.

scientific article published on 8 January 2014
Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58

scientific article published on March 1, 1991
A soluble form of prion protein in human cerebrospinal fluid: implications for prion-related encephalopathies

scientific article published on May 15, 1992
Detection of misfolded Aβ oligomers for sensitive biochemical diagnosis of Alzheimer's disease

scientific article published on 20 March 2014
Detection of prions in blood from patients with variant Creutzfeldt-Jakob disease

scientific article published on December 2016
Intraspecies transmission of BASE induces clinical dullness and amyotrophic changes

scientific article
Defined α-synuclein prion-like molecular assemblies spreading in cell culture

scientific article
Chronic wasting disease and atypical forms of bovine spongiform encephalopathy and scrapie are not transmissible to mice expressing wild-type levels of human prion protein.

scientific article published on 11 April 2012
Cerebrospinal fluid real-time quaking-induced conversion is a robust and reliable test for sporadic creutzfeldt-jakob disease: An international study

scientific article published on 30 April 2016
Structural properties of Gerstmann-Straussler-Scheinker disease amyloid protein.

scientific article published on 11 September 2003
A new function of microtubule-associated protein tau: involvement in chromosome stability

scientific article published on 25 June 2008
The efficacy of tetracyclines in peripheral and intracerebral prion infection.

scientific article
Redox metals and oxidative abnormalities in human prion diseases

scientific article published on 11 August 2005
Neuropathology of the recessive A673V APP mutation: Alzheimer disease with distinctive features.

scientific article published on 15 September 2010
Optimal plasma progranulin cutoff value for predicting null progranulin mutations in neurodegenerative diseases: a multicenter Italian study

scientific article published on 26 November 2011
Hereditary prion protein amyloidoses

scientific article published on March 1, 2003
Inter-laboratory comparison of neuropathological assessments of β-amyloid protein: a study of the BrainNet Europe consortium

scientific article published on 15 March 2008
Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI study

scientific article published on 19 October 2017
Oxidative damage to nucleic acids in human prion disease

scientific article published in April 2002
The peculiar role of the A2V mutation in amyloid-β (Aβ) 1-42 molecular assembly

scientific article
MM2-thalamic Creutzfeldt-Jakob disease: neuropathological, biochemical and transmission studies identify a distinctive prion strain.

scientific article published on 21 February 2012
A New Face for Old Antibiotics: Tetracyclines in Treatment of Amyloidoses

scientific article published on May 8, 2013
Prion deposition in olfactory biopsy of sporadic Creutzfeldt-Jakob disease

scientific article published on 01 February 2004
Inter-laboratory assessment of PrPSc typing in creutzfeldt-jakob disease: a Western blot study within the NeuroPrion Consortium

scientific article published on 2 July 2008
Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP.

scientific article published on August 2010
Transgenic fatal familial insomnia mice indicate prion infectivity-independent mechanisms of pathogenesis and phenotypic expression of disease

scientific article
Tetracycline prevents Aβ oligomer toxicity through an atypical supramolecular interaction.

scientific article
Anti-A autoantibodies in the CSF of a patient with CAA-related inflammation: A case report

scientific article published on 01 March 2011
Neuronal counts in basal nucleus of Meynert in Alzheimer disease and in simple senile dementia

scientific article published on February 26, 1983
Loss of exosomes in progranulin-associated frontotemporal dementia

scientific article published on 7 January 2016
Mutant presenilin 1 increases the expression and activity of BACE1

scientific article published on 05 February 2009
Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study

scientific article published on 8 January 2018
Complexes of amyloid-beta and cystatin C in the human central nervous system

scientific article published on January 2009
A Case of Dementia Parkinsonism Resembling Progressive Supranuclear Palsy Due to Mutation in the Tau Protein Gene

scientific article published on October 1, 2003
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia

scientific article
Sporadic Creutzfeldt-Jakob disease: the extent of microglia activation is dependent on the biochemical type of PrPSc

scientific article published on 01 October 2005
Neuropathological and clinical phenotype of an Italian Alzheimer family with M239V mutation of presenilin 2 gene.

scientific article published in March 2004
Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene.

scientific article published in November 2003

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