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ITALIAN JOURNAL OF PEDIATRICS, ISSN 1720-8424, 2009, Volume 35
"Dravet syndrome" (DS) previously named severe myoclonic epilepsy of infancy (SMEI), or epilepsy with polymorphic seizures, is a rare disorder characterized by... 
PEDIATRICS
Journal Article
Italian Journal of Pediatrics, ISSN 1720-8424, 09/2009, Volume 35, Issue 27, pp. 27 - 27
"Dravet syndrome" (DS) previously named severe myoclonic epilepsy of infancy (SMEI), or epilepsy with polymorphic seizures, is a rare disorder characterized by... 
Journal Article
Epilepsia, ISSN 0013-9580, 03/2013, Volume 54, Issue 3, pp. 425 - 436
Journal Article
by Panagiotakaki, Eleni and De Grandis, Elisa and Stagnaro, Michela and Heinzen, Erin L and Fons, Carmen and Sisodiya, Sanjay and De Vries, Boukje and Goubau, Christophe and Weckhuysen, Sarah and Kemlink, David and Scheffer, Ingrid and Lesca, Gaëtan and Rabilloud, Muriel and Klich, Amna and Ramirez-Camacho, Alia and Ulate-Campos, Adriana and Campistol, Jaume and Giannotta, Melania and Moutard, Marie-Laure and Doummar, Diane and Hubsch-Bonneaud, Cecile and Jaffer, Fatima and Cross, Helen and Gurrieri, Fiorella and Tiziano, Danilo and Nevsimalova, Sona and Nicole, Sophie and Neville, Brian and Van Den Maagdenberg, Arn M. J. M and Mikati, Mohamad and Goldstein, David B and Vavassori, Rosaria and Arzimanoglou, Alexis and Bassi, Maria Teresa and Borgatti, Renato and Cernetti, Roberta and Di Rosa, Gabriella and Franchini, Filippo and Gambardella, Antonio and Giacanelli, Manlio and Gobbi, Giuseppe and Granata, Tiziana and Guerrini, Renzo and Incorpora, Gemma and Nardocci, Nardo and Neri, Giovanni and Ragona, Francesca and Santucci, Margherita and Sartori, Stefano and Veneselli, Edvige and Vigevano, Federico and Zucca, Claudio and Aicardi, J and An, I and Arbues, A.S and Arzimanoglou, A and Bahi-Buisson, N and Barthez, M.-A and Billette de Villemeur, T and Bourgeois, M and Bru, M and Chabrol, B and Chaigne, D and Chaunu, M.P and Chaunu, C and Cournelle, A.M and Davoine, C.-S and De St Martin, A and Deny, B and Desguerres, I and Des Portes, V and Doummar, D and Dulac, O and Dusser, A and Gerard, M and Gitiaux, C and Godet Kiesel, I and Gokben, S and Goutieres, F and Guerrin, M.-H and Heron-Longe, B and Hubsch-Bonneaud, C and Hully, M and Husson, M and Husson, Ch and Kaminska, A and Laroche, C and Lazaro, L and Lepine, A and Magy, L and Marchal, C and Michel, J and Milh, M and Motte, J and Moutard, M.L and Napuri, S and Nassogne, M.C and Neau, J.P and Nicole, S and Panagiotakaki, Eleni and ... and IBAHC Consortium and French AHC Consortium and Int AHC Consortium and International AHC Consortium and Italian IBAHC Consortium and The French AHC Consortium and The Italian IBAHC Consortium and The International AHC Consortium
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 09/2015, Volume 10, Issue 1, p. 123
Journal Article
Pediatrics International, ISSN 1328-8067, 04/2010, Volume 52, Issue 2, p. e72
Journal Article
Epilepsy Research, ISSN 0920-1211, 2010, Volume 93, Issue 2, pp. 107 - 114
Journal Article
Brain and Development, ISSN 0387-7604, 2002, Volume 24, Issue 8, pp. 766 - 769
The occurrence of seizures in patients with fragile X syndrome (Fra-X) is reported. Among the 30 patients, six had epilepsy that was particularly severe and... 
Epilepsy | Fragile X syndrome | epilepsy | CLINICAL NEUROLOGY | fragile X syndrome | Action Potentials - physiology | Fragile X Syndrome - physiopathology | Humans | Adolescent | Drug Resistance - physiology | Child, Preschool | Male | Electroencephalography | Epilepsy - physiopathology | Child | Cerebral Cortex - physiopathology
Journal Article
Pediatric Neurology, ISSN 0887-8994, 2004, Volume 30, Issue 2, pp. 107 - 110
The objective of this study was to assess brain involvement through the presence of antineuronal antibodies in Pediatric Autoimmune Neuropsychiatric Disorders... 
MOVEMENT-DISORDERS | CHOREA | TOURETTES-SYNDROME | PEDIATRICS | RHEUMATIC-FEVER | ANTINEURONAL ANTIBODIES | CLINICAL NEUROLOGY | CHILDREN
Journal Article
Seizure : the Journal of the British Epilepsy Association, ISSN 1059-1311, 07/2015, Volume 29, p. 90
Purpose: To determine clinical phenotypes, evolution and genetic background of a large family with a combination of two unusual forms of reflex epilepsies.... 
Journal Article
Journal of Pediatrics, ISSN 0022-3476, 08/2008, Volume 153, Issue 2, p. 299
Journal Article
The Journal of Pediatrics, ISSN 0022-3476, 08/2008, Volume 153, Issue 2, p. 299
Journal Article
Pediatric Neurology, ISSN 0887-8994, 2007, Volume 37, Issue 3, pp. 209 - 211
Polyneuritis cranialis is a rare disorder of multiple cranial nerve palsies without spinal cord involvement. The case reported is of a 10-year-old boy with... 
Pediatrics | Neurology | PEDIATRICS | IGG ANTIBODY | NERVES | CLINICAL NEUROLOGY | MILLER-FISHER-SYNDROME | GUILLAIN-BARRE-SYNDROME | Immunoglobulins, Intravenous - therapeutic use | Humans | Male | Cranial Nerve Diseases - drug therapy | Child | Neuritis - drug therapy | Recovery of Function | Immunoglobulins
Journal Article
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