C
Carlo Alberto Tassinari
Researcher at University of Bologna
Publications - 274
Citations - 13053
Carlo Alberto Tassinari is an academic researcher from University of Bologna. The author has contributed to research in topics: Epilepsy & Ictal. The author has an hindex of 61, co-authored 273 publications receiving 12435 citations. Previous affiliations of Carlo Alberto Tassinari include University of Wisconsin-Madison & University of Turku.
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Journal ArticleDOI
Glossary of descriptive terminology for ictal semiology: report of the ILAE task force on classification and terminology.
Warren T. Blume,Hans Lüders,Eli M. Mizrahi,Carlo Alberto Tassinari,Walter van Emde Boas,Jerome Engel +5 more
TL;DR: The present study focuses on EPILEPTIC SEIZURE SEMIOLOGY, a subset of Epilepsy Research, which aims to clarify the meaning of “seizure” and “disruption” in order to facilitate diagnosis and treatment.
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Polygraphic study of the episodic diurnal and nocturnal (hypnic and respiratory) manifestations of the Pickwick syndrome.
TL;DR: The authors are convinced that the majority of individuals suffering from the pickwickian syndrome drowse during the day and sleep badly at night because of a primary disturbance in the wakefulness-sleep regulation which as such is based on their obesity.
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Childhood Epileptic Encephalopathy with Diffuse Slow Spike‐Waves (otherwise known as “Petit Mal Variant”) or Lennox Syndrome
Henri Gastaut,J. Roger,R. Soulayrol,Carlo Alberto Tassinari,H. Régis,C. Dravet,R. Bernard,Pinsard N,Saint-Jean M +8 more
TL;DR: La contribution personnelle des auteurs se limite donc à préciser certaines données séméiologiques, cliniques aussi bien qu’électroencéphalographiques, et à fournir des considérations d'ordre diagnostique, étiologique, thérapeutique and physiopathogénique.
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Coeliac disease, epilepsy, and cerebral calcifications
Giuseppe Gobbi,F. Bouquet,L. Greco,A Lambertini,Carlo Alberto Tassinari,Alessandro Ventura,M.G. Zaniboni +6 more
TL;DR: Cases of "atypical Sturge-Weber syndrome" (characterised by serpiginous cerebral calcifications and epilepsy without facial port-wine naevus) should be reviewed, and CD should be ruled out in all cases of epilepsy and cerebral calcification of unexplained origin.
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Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy
José Manuel Morante-Redolat,Ana Gorostidi-Pagola,Salomé Piquer-Sirerol,Amets Sáenz,Juan José Poza,Juan Galán,Stefan Gesk,Theologia Sarafidou,Victor F. Mautner,Simona Binelli,Eike Staub,Bernd Hinzmann,Lisa French,Jean François Prud'homme,D. Passarelli,Paolo Scannapieco,Carlo Alberto Tassinari,Giuliano Avanzini,Jose Felix Marti-Masso,Lan Kluwe,Panagiotis Deloukas,Nicholas K. Moschonas,Roberto Michelucci,Reiner Siebert,Carlo Nobile,Jordi Pérez-Tur,Adolfo López de Munain +26 more
TL;DR: It is demonstrated that the LGI1 protein, which contains several leucine-rich repeats, is expressed ubiquitously in the neuronal cell compartment of the brain and provides evidence for genetic heterogeneity within this disorder.