His primary areas of study are Amyloid, Pathology, Virology, Peptide and Disease. His Amyloid research is multidisciplinary, relying on both Immunology, Ataxia, Genetics and Amyloidosis. His Pathology study frequently draws parallels with other fields, such as Cerebral cortex.
Fabrizio Tagliavini interconnects Pathogenesis, Phenotype, Bovine spongiform encephalopathy, Prion protein and PrPSc Proteins in the investigation of issues within Virology. His Peptide research incorporates elements of Fibril, Molecular biology, Protein structure and Protein secondary structure. His Disease research includes elements of Concordance and Central nervous system disease.
His primary areas of investigation include Pathology, Disease, Frontotemporal dementia, Amyloid and Virology. His Pathology study frequently intersects with other fields, such as Cerebral cortex. His work in Frontotemporal dementia addresses subjects such as Genetics, which are connected to disciplines such as Frontotemporal lobar degeneration.
His Amyloid study combines topics from a wide range of disciplines, such as Biochemistry, Peptide and Amyloidosis. His study in Peptide is interdisciplinary in nature, drawing from both Fibril and Molecular biology. His research in Virology intersects with topics in Scrapie, Bovine spongiform encephalopathy, Prion protein and PRNP.
Fabrizio Tagliavini mostly deals with Frontotemporal dementia, Disease, C9orf72, Atrophy and Internal medicine. Fabrizio Tagliavini has included themes like Audiology, Apathy, Cognition, Neuroscience and Cohort in his Frontotemporal dementia study. His Disease research also works with subjects such as
The various areas that Fabrizio Tagliavini examines in his Atrophy study include Gastroenterology, Temporal lobe, Neurodegeneration, Gene and Neurology. While the research belongs to areas of Internal medicine, Fabrizio Tagliavini spends his time largely on the problem of Oncology, intersecting his research to questions surrounding Cerebrospinal fluid and Grey matter. His Dementia study contributes to a more complete understanding of Pathology.
Fabrizio Tagliavini mainly investigates Frontotemporal dementia, C9orf72, Atrophy, Pathology and Internal medicine. His research integrates issues of Phenotype, White matter and Gene mutation in his study of Frontotemporal dementia. His research on C9orf72 also deals with topics like
His work on Scrapie, Alzheimer's disease and Dementia as part of general Pathology study is frequently connected to Uncinate fasciculus, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them. He combines subjects such as Endocrinology and Oncology with his study of Internal medicine. His work deals with themes such as Proteases, Molecular neuroscience and Biochemistry, Protein folding, which intersect with Amyloid.
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Neurotoxicity of a prion protein fragment
Gianluigi Forloni;Nadia Angeretti;Roberto Chiesa;Enrico Monzani.
Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob disease
Cristina Casalone;Gianluigi Zanusso;Pierluigi Acutis;Sergio Ferrari.
Proceedings of the National Academy of Sciences of the United States of America (2004)
Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau.
Orso Bugiani;Jill R. Murrell;Giorgio Giaccone;Masato Hasegawa.
Journal of Neuropathology and Experimental Neurology (1999)
Apoptosis mediated neurotoxicity induced by chronic application of β amyloid fragment 25–35
Gianluigi Forloni;Roberto Chiesa;Simona Smiroldo;Laura Verga.
A recessive mutation in the APP gene with dominant-negative effect on amyloidogenesis.
Giuseppe Di Fede;Marcella Catania;Michela Morbin;Giacomina Rossi.
Reversion of prion protein conformational changes by synthetic b-sheet breaker peptides
Claudio Soto;Richard J Kascsak;Gabriela P Saborío;Pierre Aucouturier.
The Lancet (2000)
Staging of Neurofibrillary Pathology in Alzheimer's Disease: A Study of the BrainNet Europe Consortium
Irina Alafuzoff;Thomas Arzberger;Safa Al-Sarraj;Istvan Bodi.
Brain Pathology (2008)
Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis
Jonathan D Rohrer;Jennifer M Nicholas;Jennifer M Nicholas;David M Cash;John van Swieten.
Lancet Neurology (2015)
Preamyloid deposits in the cerebral cortex of patients with Alzheimer's disease and nondemented individuals
Fabrizio Tagliavini;Giorgio Giaccone;Blas Frangione;Orso Bugiani.
Neuroscience Letters (1988)
Sporadic human prion diseases: molecular insights and diagnosis
Gianfranco Puoti;Alberto Bizzi;Gianluigi Forloni;Jiri G Safar.
Lancet Neurology (2012)
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