P
Paolo Tinuper
Researcher at University of Bologna
Publications - 327
Citations - 11586
Paolo Tinuper is an academic researcher from University of Bologna. The author has contributed to research in topics: Epilepsy & Ictal. The author has an hindex of 51, co-authored 296 publications receiving 9834 citations. Previous affiliations of Paolo Tinuper include University of Melbourne & Academy for Urban School Leadership.
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Journal ArticleDOI
Fatal Familial Insomnia, a Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
R. Medori,Hans Juergen Tritschler,Andréa C. LeBlanc,Federico Villare,Valeria Manetto,Hsiao Ying Chen,Run Xue,Suzanne M. Leal,Pasquale Montagna,Pietro Cortelli,Paolo Tinuper,Patrizia Avoni,M. Mochi,Agostino Baruzzi,Jean J. Hauw,Jurg Ott,Elio Lugaresi,Lucila Autilio-Gambetti,Pierluigi Gambetti +18 more
TL;DR: Fatal familial insomnia is a prion disease with a mutation in codon 178 of the PrP gene, but the disease phenotype seems to differ from that of previously described kindreds with the same point mutation.
Journal ArticleDOI
Fatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei
Elio Lugaresi,R. Medori,Pasquale Montagna,Agostino Baruzzi,Pietro Cortelli,Alessandra Lugaresi,Paolo Tinuper,Marco Zucconi,Pierluigi Gambetti +8 more
TL;DR: The thalamus is affected in diffuse degenerative processes of the nervous system and it has not been established whether a genetically determined degenerative disease may be limited in patients with this organ.
Journal ArticleDOI
Nocturnal frontal lobe epilepsy. A clinical and polygraphic overview of 100 consecutive cases.
Federica Provini,Giuseppe Plazzi,Paolo Tinuper,Stefano Vandi,Elio Lugaresi,Pasquale Montagna +5 more
TL;DR: It is believed that the detailed clinical and videoEEG characterization of patients with NFLE represents the first step towards a better understanding of the pathogenic mechanisms and different clinical outcomes of the various seizure types that constitute the syndrome.
Journal ArticleDOI
EFNS Guideline on the Management of Status Epilepticus in Adults
Hartmut Meierkord,Paul Boon,Bernt A. Engelsen,Bernt A. Engelsen,K. Göcke,Simon Shorvon,Paolo Tinuper,Martin Holtkamp +7 more
TL;DR: The objective of the current article was to review the literature and discuss the degree of evidence for various treatment strategies for status epilepticus (SE) in adults and reach recommendations based on this literature and on judgement of the relevance of the references to the subject.
Journal ArticleDOI
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
Mikko Muona,Samuel F. Berkovic,Leanne M. Dibbens,Karen Oliver,Snezana Maljevic,Marta A. Bayly,Tarja Joensuu,Laura Canafoglia,Silvana Franceschetti,Roberto Michelucci,Salla Markkinen,Sarah E. Heron,Michael S. Hildebrand,Eva Andermann,Frederick Andermann,Antonio Gambardella,Paolo Tinuper,Laura Licchetta,Ingrid E. Scheffer,Ingrid E. Scheffer,Ingrid E. Scheffer,Chiara Criscuolo,Alessandro Filla,Edoardo Ferlazzo,Jamil Ahmad,Adeel Ahmad,Betül Baykan,Edith Said,Edith Said,Meral Topçu,Patrizia Riguzzi,Mary D. King,Mary D. King,Cigdem Ozkara,Danielle M. Andrade,Bernt A. Engelsen,Bernt A. Engelsen,Arielle Crespel,Matthias Lindenau,Ebba Lohmann,Ebba Lohmann,Veronica Saletti,João Massano,Michael Privitera,Alberto J. Espay,Birgit Kauffmann,Michael Duchowny,Michael Duchowny,Rikke S. Møller,Rachel Straussberg,Zaid Afawi,Zaid Afawi,Bruria Ben-Zeev,Bruria Ben-Zeev,Kaitlin E. Samocha,Mark J. Daly,Mark J. Daly,Steven Petrou,Steven Petrou,Holger Lerche,Aarno Palotie,Anna-Elina Lehesjoki +61 more
TL;DR: In insights into the molecular genetic basis of PME, the role of de novo mutations in this disease entity is shown and their phenotypic spectra are expanded.