L
Lino Nobili
Researcher at University of Genoa
Publications - 303
Citations - 10705
Lino Nobili is an academic researcher from University of Genoa. The author has contributed to research in topics: Epilepsy & Medicine. The author has an hindex of 57, co-authored 259 publications receiving 8396 citations. Previous affiliations of Lino Nobili include University of Catania & Istituto Giannina Gaslini.
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Psychobiological personality traits of children and adolescents with disorders of arousal.
Katherine Turner,Anna Castelnovo,Lampros Perogamvros,C. Robert Cloninger,Andrea Galbiati,A. Bertolotti,Paola Proserpio,Michele Terzaghi,Raffaele Manni,Luigi Ferini Strambi,Lino Nobili,Mauro Manconi,Maria Paola Canevini,Elena Zambrelli +13 more
TL;DR: In this paper , the authors compared the personality profile of children and adolescents with and without disorders of arousal using the Junior Temperament and Character Inventory (JTCI) and found that those with disorders of a disorder reached significantly higher levels compared to their control group in total PADSS (p < 0.0001) and in total SDSC (p = 0.005), harm avoidance, self-transcendence, and lower scores on the self-directedness subscale.
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An explorative assessment of antioxidant and inflammatory biomarkers for identification of prodromal Parkinson's disease (PD)
Jonica Campolo,Renata De Maria,Lorena Cozzi,Marina Parolini,Paola Proserpio,Lino Nobili,Giorgio Gelosa,Immacolata Piccolo,Paolo Marraccini +8 more
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Efficacy of Ketamine Use in Refractory Status Epilepticus Associated With Hemimegalencephaly.
Giacomo Brisca,Daniela Pirlo,Giulia Prato,Domenico Tortora,Laura Siri,Lino Nobili,Giacomo Tardini,Alessandro Consales,Andrea Moscatelli,Silvia Buratti +9 more
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Scoliosis with cognitive impairment in a girl with 8q11.21q11.23 microdeletion and SNTG1 disruption.
Elisa Tassano,Patrizia Ronchetto,Mariasavina Severino,Maria Teresa Divizia,Margherita Lerone,Sara Uccella,Lino Nobili,Elisa Tavella,Cristina Morerio,Domenico Coviello,Michela Malacarne +10 more
TL;DR: In this paper, a de novo interstitial deletion 8q11.21q 11.2 disrupting SNTG1 gene, identified by array-CGH in a girl with cognitive impairment and a scoliosis that 'appears' like to IS, was described.