Bacchelli E;Ceroni F;Pinto D;Lomartire S;Giannandrea M;D'Adamo P;Bonora E;Parchi P;Tancredi R;Battaglia A;Maestrini E, A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder., «JOURNAL OF NEURODEVELOPMENTAL DISORDERS», 2014, 6, Article number: 17 , pp. 1 - 11 [Scientific article]Open Access
Bonora, E.; Graziano, C.; Minopoli, F.; Bacchelli, E.; Magini, P.; Diquigiovanni, C.; Lomartire, S.; Bianco, F.; Vargiolu, M.; Parchi, P.; Marasco, E.; Mantovani, V.; Rampoldi, L.; Trudu, M.; Parmeggiani, A.; Battaglia, A.; Mazzone, L.; Tortora, G.; Maestrini, E.; Seri, M.; Romeo, G., Corrigendum: Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients(EMBO Mol Med, (2014), 6, (795–809), 10.1002/emmm.201303235), «EMBO MOLECULAR MEDICINE», 2014, 6, pp. 1639 - 1639 [Scientific article]
Cortelli, P.; Fabbri, M.; Calandra-Buonaura, G.; Capellari, S.; Tinuper, P.; Parchi, P.; Lugaresi, E., Gait disorders in fatal familial insomnia, «MOVEMENT DISORDERS», 2014, 29, pp. 420 - 424 [Scientific article]
Bonora E;Graziano C;Minopoli F;Bacchelli E;Magini P;Diquigiovanni C;Lomartire S;Bianco F;Vargiolu M;Parchi P;Marasco E;Mantovani V;Rampoldi L;Trudu M;Parmeggiani A;Battaglia A;Mazzone L;Tortora G;Maestrini E;Seri M;Romeo G;IMGSAC, Maternally inherited genetic variants of CADPS2 are present in Autism Spectrum Disorders and Intellectual Disability patients., «EMBO MOLECULAR MEDICINE», 2014, 6, pp. 795 - 809 [Scientific article]Open Access
Franco Cardone; Serena Principe; Maria Eugenia Schininà; Bruno Maras; Sabina Capellari; Piero Parchi; Silvio Notari; Laura Di Francesco; Anna Poleggi; Roberta Galeno; Ramona Vinci; Vittorio Mellina; Susanna Almonti; Anna Ladogana; Maurizio Pocchiari, Mutant PrPCJD prevails over wild-type PrPCJD in the brain of V210I and R208H genetic Creutzfeldt-Jakob disease patients, «BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS», 2014, 454, pp. 289 - 294 [Scientific article]
Moghadam KK;Pizza F;La Morgia C;Franceschini C;Tonon C;Lodi R;Barboni P;Seri M;Ferrari S;Liguori R;Donadio V;Parchi P;Cornelio F;Inzitari D;Mignarri A;Capocchi G;Dotti MT;Winkelmann J;Lin L;Mignot E;Carelli V;Plazzi G, Narcolepsy is a common phenotype in HSAN IE and ADCA-DN, «BRAIN», 2014, 137, pp. 1643 - 1655 [Scientific article]
D. Saverioni;S. Notari;S. Capellari;I. Poggiolini;A. Giese;H. A. Kretzschmar;P. Parchi, Analyses of Protease Resistance and Aggregation State of Abnormal Prion Protein across the Spectrum of Human Prions, «THE JOURNAL OF BIOLOGICAL CHEMISTRY», 2013, 288, pp. 27972 - 27985 [Scientific article]
Gelpi E.; Soler Insa J.M.; Parchi P.; Saverioni D.; Yagüe J.; Nos C.; Martínez-Saez E.; Ribalta T.; Ferrer I.; Sanchez-Valle R., Atypical neuropathological sCJD-MM phenotype with abundant white matter Kuru-type plaques sparing the cerebellar cortex., «NEUROPATHOLOGY», 2013, 33, pp. 204 - 208 [Scientific article]
N. Mattsson;U. Andreasson;S. Persson;M. C. Carrillo;S. Collins;S. Chalbot;N. Cutler;D. Dufour-Rainfray;A. M. Fagan;N. H. H;G. R. Hsiung;B. Hyman;K. Iqbal;D. R. Lachno;A. Lleó;P. Lewczuk;J. L. Molinuevo;P. Parchi;A. Regeniter;R. Rissman;H. Rosenmann;G. Sancesario;J. Schröder;L. M. Shaw;C. E. Teunissen;J. Q. Trojanowski;H. Vanderstichele;M. Vandijck;M. M. Verbeek;H. Zetterberg;K. Blennow;S. A. Käser;Alzheimer's Association QC Program Work Group, CSF biomarker variability in the Alzheimer's Association quality control program., «ALZHEIMER'S & DEMENTIA», 2013, 9, pp. 251 - 261 [Scientific article]
P. Parchi;S. Capellari, Prion disease: diagnostic value of cerebrospinal fluid markers., «NATURE REVIEWS. NEUROLOGY», 2013, 9, pp. 10 - 11 [Scientific article]
I. Poggiolini;D. Saverioni;P. Parchi, Prion protein misfolding, strains, and neurotoxicity: an update from studies on Mammalian prions., «INTERNATIONAL JOURNAL OF CELL BIOLOGY», 2013, 2013, pp. 910314 - 910314 [Scientific article]
Parchi P.; de Boni L.; Saverioni D.; Cohen M.L.; Ferrer I.; Gambetti P.; Gelpi E.; Giaccone G.; Hauw J.J.; Höftberger R.; Ironside J.W.; Jansen C.; Kovacs G.G.; Rozemuller A.; Seilhean D.; Tagliavini F.; Giese A.; Kretzschmar H.A., Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA., «ACTA NEUROPATHOLOGICA», 2012, 124, pp. 517 - 529 [Scientific article]
Popova S.N.; Tarvainen I.; Capellari S.; Parchi P.; Hannikainen P.; Pirinen E.; Haapasalo H.; Alafuzoff I., Divergent clinical and neuropathological phenotype in a Gerstmann-Sträussler-Scheinker P102L family., «ACTA NEUROLOGICA SCANDINAVICA», 2012, 126, pp. 315 - 323 [Scientific article]
Jansen C.; Parchi P.; Capellari S.; Ibrahim-Verbaas C.A.; Schuur M.; Strammiello R.; Corrado P.; Bishop M.T.; van Gool W.A.; Verbeek M.M.; Baas F.; van Saane W.; Spliet W.G.; Jansen G.H.; van Duijn C.M.; Rozemuller A.J., Human prion diseases in the Netherlands (1998-2009): clinical, genetic and molecular aspects., «PLOS ONE», 2012, 7, Article number: e36333 , pp. 1 - 10 [Scientific article]Open Access
Parchi P.; Saverioni D., Molecular pathology, classification, and diagnosis of sporadic human prion disease variants., «FOLIA NEUROPATHOLOGICA», 2012, 50, pp. 20 - 45 [Scientific article]
