Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Raffaella, Moretti"'
Autor:
Daria Coppola, Raffaella Moretti
Publikováno v:
Italiano LinguaDue, Vol 12, Iss 2 (2021)
Il presente contributo si inserisce nel panorama degli studi sull’educazione linguistica intesa come ambito integrato di studio di tutte le lingue che si parlano e si apprendono a scuola (L1, L2, LS) e, più in generale, di tutti i codici e le vari
Externí odkaz:
https://doaj.org/article/0163b5b91ed74dee9443a690e707e0ca
Autor:
Stephane Besnard, Clotilde Nardin, Elsa Lyon, Thomas Debroucker, Roxana Arjmand, Raffaella Moretti, Hervé Pochat
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Viral infection with SARS-CoV-2 has a neurological tropism that may induce an encephalopathy. In this context, electroencephalographic exploration (EEG) is indicated as a diagnostic argument correlated with lumbar puncture, biology, and imaging. We p
Externí odkaz:
https://doaj.org/article/8f274d02ed9c49f78eea38f0bfaf84d3
Autor:
Julien Buratti, Isabelle Gourfinkel-An, Oriane Trouillard, Raffaella Moretti, Cyril Mignot, Delphine Bouteiller, Vincent des Portes, Patricia Moreau, Christel Depienne, Boris Keren, Agnès Rastetter, Lionel Arnaud, Joseph Toulouse, Caroline Nava, Eric LeGuern
Publikováno v:
European Journal of Paediatric Neurology. 33:121-124
Background Variants in SCN1A gene, encoding the voltage-gated sodium channel Nav1.1, are associated with distinct epilepsy syndromes ranging from the relatively benign genetic epilepsy with febrile seizures plus (GEFS+) to Dravet syndrome, a severe d
Autor:
Pia Gellert, Guido Rubboli, Elena Gardella, Katrine M. Johannesen, Claudia M Bonardi, Gaetan Lesca, Carlo Alberto Tassinari, Cyril Mignot, José M. Serratosa, Chiara Reale, Raffaella Moretti, Rikke S. Møller, Gabrielle Rudolf, Beatriz G. Giráldez
Publikováno v:
Bonardi, C M, Mignot, C, Serratosa, J M, Giraldez, B G, Moretti, R, Rudolf, G, Reale, C, Gellert, P M, Johannesen, K M, Lesca, G, Tassinari, C A, Gardella, E, Møller, R S & Rubboli, G 2020, ' Expanding the clinical and EEG spectrum of CNKSR2-related encephalopathy with status epilepticus during slow sleep (ESES) ', Clinical Neurophysiology, vol. 131, no. 5, pp. 1030-1039 . https://doi.org/10.1016/j.clinph.2020.01.020
Objective To investigate the clinical and EEG features of Encephalopathy with Status Epilepticus during slow Sleep (ESES) related to CNKSR2 pathogenic variants. Methods Detailed clinical history, repeated wakefulness/overnight sleep EEGs, brain MRI w
This article takes into account results from two classroom research projects and analyses validity and effectiveness of dialogical cooperative techniques for plurilingual education. The first experimental study focuses on language learning strategies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8390e2c89d7979beeb91fed5f77fca2c
https://doi.org/10.30687/978-88-6969-501-8/014
https://doi.org/10.30687/978-88-6969-501-8/014
Autor:
Hervé Pochat, Thomas Debroucker, Elsa Lyon, Roxana Arjmand, Stephane Besnard, Raffaella Moretti, Clotilde Nardin
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Frontiers in Neurology
Frontiers in Neurology
Viral infection with SARS-CoV-2 has a neurological tropism that may induce an encephalopathy. In this context, electroencephalographic exploration (EEG) is indicated as a diagnostic argument correlated with lumbar puncture, biology, and imaging. We p
Autor:
Priscilla Boizeau, Luigi Titomanlio, Daniele Spiri, Giovanni Crichiutti, Davide Massano, Camille Aupiais, Corinne Alberti, Véronique Houdouin, Stéphanie Wanin, Silvia Romanello, Raffaella Moretti, Lakshmi Kanagarajah, Gian Vincenzo Zuccotti
Publikováno v:
Headache: The Journal of Head and Face Pain. 57:612-624
Background Migraine is a common cause of headache in childhood. Several studies have investigated the association between migraine and atopic diseases, mostly in the adult population. Objective This study aimed to investigate this association in chil
Autor:
Myrtille Spentchian, Cyril Mignot, Hala Soliman, Viviane Bouilleret, Suzette I. Helal, Camille Desprairies, Heather C Mefford, Sarah Weckhuysen, Delphine Héron, Caroline Nava, Raffaella Moretti, Eric LeGuern, Stéphanie Valence, Hélène Maurey
Publikováno v:
Clinical genetics
Biallelic mutations in the PLCB1 gene, encoding for a phospholipase C beta isoform strongly expressed in the brain, have been reported to cause infantile epileptic encephalopathy in only four children to date. We report here three additional patients
Autor:
Myrtille Spentchian, Hala Soliman, Suzette I. Helal, Heather C Mefford, Caroline Nava, Eric LeGuern, Delphine Héron, Camille Desprairies, Sarah Weckhuysen, Cyril Mignot, Raffaella Moretti, Stéphanie Valence, Hélène Maurey, Viviane Bouilleret
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8765c6745b4d86cd3e2ac0ee4f01a388
https://doi.org/10.1111/cge.13696/v2/response1
https://doi.org/10.1111/cge.13696/v2/response1
Autor:
Valérie C. Besson, Pooja Joshi, Valérie Faivre, Raffaella Moretti, Christiane Charriaut-Marlangue, Sonia Villapol
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 20, Iss 15, p 3809 (2019)
Volume 20
Issue 15
International Journal of Molecular Sciences, Vol 20, Iss 15, p 3809 (2019)
Volume 20
Issue 15
We recently reported that neonatal ischemia induces microglia/macrophage activation three days post-ischemia. We also found that female mice sustained smaller infarcts than males three months post-ischemia. The objective of our current study was to e