Rizzo G.; Pizza F.; Scaglione C.; Tommasoni E.; Capellari S.; Ambrosetto P.; Martinelli P., Fragile X premutation tremor/ataxia syndrome (FXTAS): a case with characteristic clinical and MR features., in: , «NEUROLOGY», 2005, 26, pp. S288 - S288 (atti di: XXXVI Congress of the Italian Neurological Sciences, Cernobbio, 8-12 ottobre 2005) [atti di convegno-abstract]
S Notari; S Capellari; A Giese; J Grassi; B Ghetti; P Gambetti; HA Kretzschmar; P Parchi, Heterogeneity of truncated fragments distinct from PrP27-30 correlates with
clinico-pathological subtypes of Creutzfeldt-Jakob disease, in: Prion 2005. Between fundamentals and society's needs, s.l, s.n, 2005, 1, pp. 268 - 268 (atti di: Prion 2005. Between fundamentals and society's needs, Dusseldorf, Germania, 19-21 ottobre 2005) [atti di convegno-abstract]
P. Parchi; S. Notari; S. Strammiello; S. Capellari, History and state of the art of PrP-res “typing” in Creutzfeldt-Jakob disease, in: Parchi, Piero, Prions: Food and drug safety, TOKIO, Springer-Verlag, 2005, pp. 77 - 95 [capitolo di libro]
C. Tonon; P. Parchi; R. Lodi; D. N. Manners; S. Capellari; A. Filla; E. Malucelli; G. Pierangeli; P. Cortelli; P. Montagna; B. Barbiroli, Prion disease: an in vivo proton magnetic resonance spectroscopy study of thalamus., in: , «NEUROLOGICAL SCIENCES», 2005, 26, pp. 221 - 221 (atti di: XXXVI Congress of the Italian Neurological Society., Cernobbio (Como), 8-12 Ottobre 2005) [atti di convegno-abstract]
C. Tonon; D.N. Manners; P. Parchi; R. Lodi; S. Capellari; A. Filla; G. Pierangeli; C. Testa; P. Cortelli; P. Montagna; B. Barbiroli., Prion disease: diffusion-weighted mri shows abnormalities in white and deep grey matter, in: , «NEUROLOGICAL SCIENCES», 2005, 26, pp. 79 - 80 (atti di: XXXVI Congress of the Italian Neurological Society, Cernobbio (Como), 8-12 Ottobre 2005) [atti di convegno-abstract]
S. Principe; L. Dimiziani; S. Notari; Q.G. Liu; F. Cardone; A. De Pascalis; S. Capellari;
P. Roepstorff; B. Maras; P. Parchi; M.E. Schininà; M. Pocchiari, Quantitative mass spectrometry analysis of the PrPTSE allotypes present in the
brain of a diseased individual carrying the R208H mutation., in: Prion 2005. Between fundamentals and society's needs, s.l, s.n, 2005, 1, pp. 308 - 308 (atti di: Prion 2005. Between fundamentals and society's needs, Dusseldorf, 19-21 ottobre 2005) [atti di convegno-abstract]
Lodi R.; Parchi P.; Tonon C.; Manners D.; Capellari S.; Filla A.; Malucelli E.; Pierangeli G.; Cortelli P.; Montagna P.; Barbiroli B., Reduced in Vivo thalamic N-Acetyl-Aspartate is a Diagnostic Marker of Prion Disease, in: Abstracts - America Academy of Neurology 57th Annual Meeting, «NEUROLOGY», 2005, 64, pp. A410 - A410 (atti di: America Academy of Neurology 57th Annual Meeting, Miami, 9 - 16 April) [atti di convegno-abstract]
C. Tonon; P. Parchi; R. Lodi; D.N. Manners; S. Capellari; A. Filla; E. Malucelli; G. Pierangeli; P. Cortelli; P. Montagna; B. Barbiroli, Use of in vivo proton magnetic resonance spectroscopy in the differential diagnosis of prion diseases, in: 2 nd The new prion biology: basic science, diagnosis and therapy, s.l, s.n, 2005, pp. 88 - 88 (atti di: 2nd International Symposium on the new prion biology: basic science, diagnosis and therapy., Venezia, Italia, 7-9 Aprile 2005) [atti di convegno-abstract]
M. Cescatti; S. Capellari; P. Gambetti; P. Parchi, Variations at the Calpain 1 gene locus in sporadic Creutzfeldt-Jakob disease, in: Prion 2005. Between fundamentals and society's needs, s.l, s.n, 2005, 1, pp. 234 - 234 (atti di: Prion 2005. Between fundamentals and society's needs, Dusseldorf, 19-21 ottobre 2005) [atti di convegno-abstract]
NOTARI S; CAPELLARI S; GIESE A; WESTNER I; BARUZZI A.; GHETTI B; GAMBETTI P; KRETZSCHMAR HA; PARCHI P., Effects of different experimental conditions on the PrPSc core generated by protease digestion: implications for strain typing and molecular classification of CJD., «THE JOURNAL OF BIOLOGICAL CHEMISTRY», 2004, 279, pp. 16797 - 16804 [articolo]
Kong Q; Surewicz WK; Petersen RB; Zou W; Chen SG; Gambetti P; Parchi P; Capellari S; Goldfarb L; Montagna P; Lugaresi E; Piccardo P; Ghetti B., INHERITED PRION DISEASES, in: PRION BIOLOGY AND DISEASES, COLD SPRING HARBOR, NEW YORK, Cold Spring Harbor Laboratory Press, 2004, pp. 673 - 776 [capitolo di libro]
Castellani R.J.; Colucci M.; Xie Z.; Zou W.; Li C.; Parchi P.; Capellari S.; Pastore M.; Rahbar M.H.; Chen S.G.; Gambetti P., Sensitivity of 14-3-3 protein test varies in subtypes of sporadic Creutzfeldt-Jakob disease, «NEUROLOGY», 2004, 63(3), pp. 436 - 442 [articolo]
