Parchi P.; Gambetti P.; Capellari S., Genetic Creutzfeldt-Jakob Disease., in: Neurodegeneration: The molecular pathology of dementia and movement disorders., CHICHESTER, Wiley-Blackwell, 2011, pp. 336 - 345 [capitolo di libro]
Capellari S.; Strammiello R.; Saverioni D.; Kretzschmar H.; Parchi P., Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: Insights into phenotypic variability and disease pathogenesis., «ACTA NEUROPATHOLOGICA», 2011, 121, pp. 21 - 37 [articolo]
Guaraldi P.; Donadio V.; Capellari S.; Contin M.; Casadio M.C.; Montagna P.; Liguori R.; Cortelli P., Isolated noradrenergic failure in adult-onset autosomal dominant leukodystrophy., «AUTONOMIC NEUROSCIENCE: BASIC & CLINICAL», 2011, 159, pp. 123 - 126 [articolo]
Orth M.; European Huntington's Disease Network; Handley O.J.; Schwenke C.; Dunnet S.; Wild E.J.; Tabrizi S.J.; Landwehrmeyer G.B.; Capellari S.; Cortelli P.; Gallassi R.; Poda R.; Rizzo G.; Scaglione C., Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY., «JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY», 2011, 82, pp. 1409 - 1412 [replica/breve intervento]
Bonazza S; La Morgia C; Martinelli P; Capellari S, Strio-pallido-dentate calcinosis: a diagnostic approach in adult patients, «NEUROLOGICAL SCIENCES», 2011, 32(4), pp. 537 - 545 [articolo]
Jansen C.; Parchi P.; Jelles B.; Gouw AA.; Beunders G.; van Spaendonk R.M.; van de Kamp J.M.; Lemstra A.W.; Capellari S.; Rozemuller A.J., The first case of fatal familial insomnia (FFI) in the Netherlands: a patient
from Egyptian descent with concurrent four repeat tau deposits., «NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY», 2011, 37, pp. 549 - 553 [articolo]
Parchi P.; Cescatti M.; Notari S.; Schulz-Schaeffer W.J.; Capellari S.; Giese A.; Zou W.Q.; Kretzschmar H.; Ghetti B.; Brown P., Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease., «BRAIN», 2010, 133, pp. 3030 - 3042 [articolo]
Masullo C; Bizzarro A; Guglielmi V; Iannaccone E; Minicuci G; Vita MG; Capellari S; Parchi P; Servidei S, An atypical phenotype of CJD associated with the E200K mutation in the prion protein gene., «NEUROLOGICAL SCIENCES», 2010, 31(6), pp. 837 - 839 [articolo]
Kovacs GG; Sanchez-Juan P; Ströbel T; Schuur M; Poleggi A; Nocentini S;
Giannattasio C; Belay G; Bishop M; Capellari S; Parchi P; Gelpi E; Gal A; Bakos
A; Molnar MJ; Heinemann U; Zerr I; Knight RS; Mitrova E; van Duijn C; Budka H., Cathepsin D (C224T) Polymorphism in Sporadic and Genetic Creutzfeldt-Jakob
Disease, «ALZHEIMER DISEASE & ASSOCIATED DISORDERS», 2010, 24, pp. 104 - 107 [articolo]
Sabina Cevoli; Nadia Marzocchi; Sabina Capellari; Chiara Scapoli; Giulia Pierangeli; Daniela Grimaldi; Federica Naldi; L. Alberto Pini; Pasquale Montagna; Pietro Cortelli, Lack of association between five serotonin metabolism-related genes and medication overuse headache, «THE JOURNAL OF HEADACHE AND PAIN», 2010, 11, pp. 53 - 58 [articolo]Open Access
Jansen C.; Parchi P.; Capellari S.; Vermeij A.J.; Corrado P.; Baas F.; Strammiello R.; van Gool W.A.; van Swieten J.C.; Rozemuller A.J., Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP., «ACTA NEUROPATHOLOGICA», 2010, 119, pp. 189 - 197 [articolo]
Fusco D; Vargiolu M; Vidone M; Mariani E; Pennisi LF; Bonora E; Capellari S;
Dirnberger D; Baumeister R; Martinelli P; Romeo G., The RET51/FKBP52 complex and its involvement in Parkinson disease., «HUMAN MOLECULAR GENETICS», 2010, 19(14), pp. 2804 - 2816 [articolo]
Zou W.Q.; Puoti G.; Xiao X.; Yuan J.; Qing L.; Cali I.; Shimoji M.; Langeveld J.P.; Castellani R.; Notari S.; Crain B.; Schmidt R.E.; Geschwind M.; Dearmond S.J.; Cairns N.J.; Dickson D.; Honig L.; Torres J.M.; Mastrianni J.; Capellari S.; Giaccone G.; Belay E.D.; Schonberger L.B.; Cohen M.; Perry G.; Kong Q.; Parchi P.; Tagliavini F.; Gambetti P., Variably protease-sensitive prionopathy: A new sporadic disease of the prion protein., «ANNALS OF NEUROLOGY», 2010, 68, pp. 162 - 172 [articolo]
Baldin E.; Capellari S.; Provini F.; Corrado P.; Liguori R.; Parchi P.; Montagna P.; Cortelli P., A case of fatal familial insomnia in Africa., «JOURNAL OF NEUROLOGY», 2009, 256, pp. 1778 - 1779 [replica/breve intervento]
LA MORGIA, Chiara; Parchi, Piero; Capellari, Sabina; Lodi, Raffaele; Tonon, Caterina; Rinaldi, R.; Mondini, S.; Cirignotta, Fabio, "Agrypnia excitata'' in a case of sporadic Creutzfeldt-Jakob disease VV2, «JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY», 2009, 80, pp. 244 - 246 [articolo]
