R. Strammiello; S. Capellari; P. Parchi, Sporadic CJD histotyping by
means of activated microglia
profiling, in: , «CLINICAL NEUROPATHOLOGY», 2009, 28 part 3, pp. 242 - 242 (atti di: Joint Meeting
XLV Congress of the Italian Association of
Neuropathology (AINP)
XXXV Congress of the Italian Association for
Research on Brain Aging (AIRIC), Bologna, Italy,, June 3 – 6, 2009) [atti di convegno-abstract]
Ragno M.; Scarcella M.G.; Cacchiò G.; Capellari S.; Di Marzio F.; Parchi P.; Trojano L., Striatal [123] FP-CIT SPECT demonstrates dopaminergic deficit in a sporadic case of Creutzfeldt-Jakob disease., «ACTA NEUROLOGICA SCANDINAVICA», 2009, 119 (2), pp. 131 - 134 [articolo]
S. Principe; F. Cardone; L. Di Francesco; A. Giorgi; G. Mignogna; M. Sbriccoli; R. Galeno; S. Notari; S. Capellari; P. Parchi; J. Rappsilber; B. Maras; M.E. Schininà; M. Pocchiari, The role of PrP and other
proteins in prion diseases, in: , «CLINICAL NEUROPATHOLOGY», 2009, 28 part 3, pp. 238 - 238 (atti di: Joint Meeting
XLV Congress of the Italian Association of
Neuropathology (AINP)
XXXV Congress of the Italian Association for
Research on Brain Aging (AIRIC), Bologna, Italy,, June 3 – 6, 2009) [atti di convegno-abstract]
Capellari S; Corrado P; Gambetti P; Parchi P, Analysis of polymorphisms in PRNP 5' UTR region in sCJD subtypres, in: Prion 2008 abstract book, SL, sn, 2008, 1, pp. 119 - 119 (atti di: Prion 2008, Madrid, 8-10 ottobre 2008) [atti di convegno-abstract]
G G Kovacs; P Sanchez-Juan; T Strobel; M Schuur; A Poleggi; S Nocentini; C Giannattasio; G Belay; M Bishop; S Capellari; P Parchi; E Gelpi; A Gal; A Bakos; M J. Molnar; U Heinemann; I Zerr; Richar S.G. Knight; Eva Mitrova; Cornelia van Duijn; Herbert Budka, Cathepsin D (C224T) polymorphism in sporadic and genetic Creutzfeldt-Jakob disease, in: Prion 2008 abstract book, SL, sn, 2008, 1, pp. 27 - 27 (atti di: Prion 2008, Madrid, 8-10 ottobre 2008) [atti di convegno-abstract]
Notari S; Strammiello R; Capellari S; Giese A; Cescatti M; Grassi J; Ghetti B; Langeveld JP; Zou WQ; Gambetti P; Kretzschmar HA; Parchi P., Characterization of truncated forms of abnormal prion protein in
Creutzfeldt-Jakob disease., «THE JOURNAL OF BIOLOGICAL CHEMISTRY», 2008, 283, pp. 30557 - 30565 [articolo]
Ladogana A; Mellina V; Almonti S; Puopolo M; Poleggi A; Capellari S; Parchi P; Pocchiari M, Diagnostic profiles of young patients referred to the CJD Italian surveillance units, in: Prion 2008 Book of abstracts, SL, sn, 2008, 1, pp. 24 - 24 (atti di: Prion 2008, Madrid, 8-10 ottobre 2008) [atti di convegno-abstract]
Rizzo G.; Martinelli P.; Manners D.; Scaglione C.; Tonon C.; Cortelli P.; Malucelli E.; Capellari S.; Testa C.; Parchi P.; Montagna P.; Barbiroli B.; Lodi R., Diffusion-weighted brain imaging study of patients with clinical diagnosis of corticobasal degeneration, progressive supranuclear palsy and Parkinson's disease., «BRAIN», 2008, 131, pp. 2690 - 2700 [articolo]
Strammiello R; Capellari S; Parchi P, Microglial activation in sporadic CJD: regional variability and the effect of disease subtype, in: Prion 2008 abstract book, SL, sn, 2008, 1, pp. 50 - 50 (atti di: Prion 2008, Madrid, 8-10 ottobre 2009) [atti di convegno-abstract]
Kovacs GG; Alafuzoff I; Al-Sarraj S; Arzberger T; Bogdanovic N; Capellari S;
Ferrer I; Gelpi E; Kövari V; Kretzschmar H; Nagy Z; Parchi P; Seilhean D;
Soininen H; Troakes C; Budka H., Mixed Brain Pathologies in Dementia: The BrainNet Europe Consortium Experience., «DEMENTIA AND GERIATRIC COGNITIVE DISORDERS», 2008, 2008 Oct 10;26(4), pp. 343 - 350 [articolo]
A. B. Rodríguez-Martínez; M. A. Alfonso-Sánchez; J. A. Peña; R Sánchez-Valle; I. Zerr; S. Capellari; M. Calero; J. J. Zarranz and M. M. de Pancorbo, Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation, «NEUROGENETICS», 2008, 9(2), pp. 109 - 118 [articolo]
Capellari S.; Parchi P.; Cortelli P.; Avoni P.; Casadei G.P.; Bini C.; Baruzzi A.; Lugaresi E.; Pocchiari M.; Gambetti P.; Montagna P., Sporadic fatal insomnia in a fatal familial insomnia pedigree., «NEUROLOGY», 2008, 70 (11), pp. 884 - 885 [articolo]
Notari S.; Capellari S.; Langeveld J.; Giese A.; Strammiello R.; Gambetti P.; Kretzschmar H.A.; Parchi P., A refined method for molecular typing reveals that co-occurrence of PrP(Sc) types in Creutzfeldt-Jakob disease is not the rule., «LABORATORY INVESTIGATION», 2007, 87, pp. 1103 - 1112 [articolo]
Capellari S; Notari S; Cescatti M; Pegoraro E; Pantieri R; Michelucci R; Parchi P, CJD Associated with the E200K Mutation with Valine at Codon 129 on the
Mutated Allele and Methionine on the Wild Type Allele: Report of Two Cases, in: www.prion2007.com, s.l, s.n, 2007, 1, pp. 67 - 67 (atti di: prion2007, Edimburgo, 26-28 settembre 2007) [atti di convegno-abstract]
Mellina V, Equestre M; Poleggi A; Ladogana A; Almonti S; Morocutti A; Bove R; Cupini ML; Desiato MT; De Simone R; Arciprete F; Paolucci E; Brusa L; Iani C; Capellari S; Parchi P, Creutzfeldt Jakob Disease Associated with the R208H-129V Haplotype in the
Protein Gene, in: www.prion2007.com, s.l, s.n, 2007, 1, pp. 121 - 121 (atti di: prion2007, Edimburgo, 26-28 settembre 2007) [atti di convegno-abstract]
