2010 - Fellow of the American Association for the Advancement of Science (AAAS)
His main research concerns Fatal familial insomnia, Virology, Pathology, Genotype and Disease. His Fatal familial insomnia research includes elements of Genetics, Mutation, PRNP, Degenerative disease and Methionine. The Virology study combines topics in areas such as Scrapie, PrPSc Proteins, Prion protein, Bovine spongiform encephalopathy and Gene isoform.
The concepts of his Pathology study are interwoven with issues in Thalamus and Electroencephalography. His biological study spans a wide range of topics, including Phenotype, Kuru and Allele. His Disease research incorporates elements of Amino acid, Cerebral cortex and Pathogenesis.
The scientist’s investigation covers issues in Pathology, Virology, Disease, Fatal familial insomnia and Molecular biology. His Virology research is multidisciplinary, relying on both Phenotype, PrPSc Proteins, Genotype and Creutzfeldt-Jakob Syndrome, Prion protein. Pierluigi Gambetti is exploring Phenotype as part of his Gene and Genetics and Phenotype studies.
His Disease research is multidisciplinary, incorporating perspectives in Transmission, Pediatrics and Pathogenesis. His Fatal familial insomnia research includes themes of Endocrinology, Atrophy and Thalamus. His Molecular biology research incorporates themes from Cell, Neurofilament and Epitope, Antibody, Monoclonal antibody.
Pierluigi Gambetti focuses on Virology, Disease, Pathology, Prion protein and Genetics. His study in Virology is interdisciplinary in nature, drawing from both Phenotype, Bank vole, Protein Misfolding Cyclic Amplification and Genetically modified mouse. His research integrates issues of Mutation, Cerebrospinal fluid and Transmission in his study of Disease.
His study explores the link between Pathology and topics such as Diffusion MRI that cross with problems in Abnormality, Clinical course, Mri scan, Antemortem Diagnosis and Pathological. He combines subjects such as Cell cycle and Biochemistry with his study of Prion protein. As part of his studies on Genotype, he often connects relevant subjects like Fatal familial insomnia.
Pierluigi Gambetti mainly focuses on Disease, Virology, Prion protein, Pathology and Scrapie. His studies in Disease integrate themes in fields like Genetics, Cerebrospinal fluid, Mutation, Transmission and Genotype. His Virology study integrates concerns from other disciplines, such as Protein Misfolding Cyclic Amplification, Genetically modified mouse, In vivo and Bovine spongiform encephalopathy.
His Prion protein study incorporates themes from Cell cycle, Biochemistry and Cell biology. As a part of the same scientific study, Pierluigi Gambetti usually deals with the Pathology, concentrating on Phenotype and frequently concerns with Case-control study and Prospective cohort study. His work deals with themes such as PRNP and Fatal familial insomnia, which intersect with Exome sequencing.
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Classification of sporadic Creutzfeldt‐Jakob disease based on molecular and phenotypic analysis of 300 subjects
Piero Parchi;Armin Giese;Sabina Capellari;Paul Brown.
Annals of Neurology (1999)
Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.
Piero Parchi;Rudolph Castellani;Sabina Capellari;Bernardino Ghetti.
Annals of Neurology (1996)
Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity.
Glenn C. Telling;Piero Parchi;Stephen J. DeArmond;Pietro Cortelli.
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism
Lev G. Goldfarb;Robert B. Petersen;Massimo Tabaton;Paul Brown.
Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei
Elio Lugaresi;Rossella Medori;Pasquale Montagna;Agostino Baruzzi.
The New England Journal of Medicine (1986)
Fatal Familial Insomnia, a Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
Rossella Medori;Hans Juergen Tritschler;Andréa Leblanc;Federico Villare.
The New England Journal of Medicine (1992)
Parkinson disease, dementia, and alzheimer disease: Clinicopathological correlations
Fraņois Boller;Tomohiko Mizutani;Uros Roessmann;Pierluigi Gambetti.
Annals of Neurology (1980)
Sporadic and familial CJD: classification and characterisation
Pierluigi Gambetti;Qingzhong Kong;Wenquan Zou;Piero Parchi.
British Medical Bulletin (2003)
Truncated forms of the human prion protein in normal brain and in prion diseases.
Shu G. Chen;David B. Teplow;Piero Parchi;Jan K. Teller.
Journal of Biological Chemistry (1995)
Familial and sporadic fatal insomnia.
Pasquale Montagna;Pierluigi Gambetti;Pietro Cortelli;Elio Lugaresi.
Lancet Neurology (2003)
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