Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Adina Ilea"'
Autor:
Camille Desprairies, Stéphane Auvin, Hala Nasser, Adina Ilea, Blandine Dozières-Puyravel, Vanina Bellavoine, Catherine Delanoë
Publikováno v:
European Journal of Paediatric Neurology. 22:837-844
Epileptic encephalopathy with continuous spikes-and-waves during sleep (EE-CSWS) is a rare childhood epilepsy syndrome characterized by a regression in cognitive, behavioral and psychiatric functioning, seizures and a specific electroencephalographic
Autor:
Vanina Bellavoine, Hala Nasser, Stéphane Auvin, Adina Ilea, Blandine Dozières-Puyravel, Catherine Delanoë
Publikováno v:
Developmental medicine and child neurologyReferences. 62(5)
Aim To analyse the effects of felbamate in refractory infantile spasms/West syndrome. Method We conducted a 10-year retrospective study of infants (including all infants younger than 18mo) treated with felbamate for electroencephalography-recorded ep
Autor:
Adina Ilea
Publikováno v:
Critical Criminology. 26:357-372
The ‘sex offender’ is the subject of intense media focus, public attention, political manipulation, as well as psychological, sociological and correctional interest. He is categorized, classified and vilified by the public, the media, the psy-dis
Publikováno v:
Epilepsy & Behavior. 74:59-63
Aim Report the use of perampanel treatment in children with Lennox–Gastaut syndrome (LGS). Method We conducted a prospective study of 13 LGS patients (seven male; mean age, 12.8 years) treated with adjunctive perampanel therapy. Perampanel was init
Autor:
Neli Le Morvan, Vanina Bellavoine, Stéphane Auvin, Catherine Delanoë, Elisa Lopez-Hernandez, Adina Ilea, Hala Nasser
Publikováno v:
Epileptic Disorders. 19:137-146
Typical absence seizures are observed in various epilepsy syndromes, however, few series have focused on early-onset absence epilepsy (EOAE). We aimed to evaluate the occurrence of this seizure type in children under 4 years of age in order to evalua
Autor:
Giuseppe Merla, Alison M. Muir, Boris Keren, Natascia Malerba, Chontelle King, Ingrid E. Scheffer, Peter Kannu, Brian H.Y. Chung, Gemma Poke, Mahendranath Moharir, Michele Germano, Carolina Fischinger Moura de Souza, Jasmine L.F. Fung, Guillem de Valles-Ibáñez, Heather C Mefford, Thorsten Stanley, Lynette G. Sadleir, Zhuo Shao, Anne Isabelle Vermersch, Cyril Mignot, Adina Ilea, Cheuk Wing Fung, Suzanne Davis
Publikováno v:
EpilepsiaREFERENCES. 60(11)
Pathogenic variants in GNB5 cause an autosomal recessive neurodevelopmental disorder with neonatal sinus bradycardia. Seizures or epilepsy occurred in 10 of 22 previously reported cases, including 6 children from one family. We delineate the epilepto
Autor:
Jean-Philippe Puech, Antoinette Gelot, Elisa Lopez Hernandez, Hala Nasser, Catherine Caillaud, Stéphane Auvin, Adina Ilea, Samia Pichard, Blandine Dozières-Puyravel, Catherine Delanoë, Monique Elmaleh-Bergès
Publikováno v:
Developmental medicine and child neurologyReferences. 62(4)
Neuronal ceroid lipofuscinoses (NCLs) are rare, progressive disorders. Through this series of 20 patients with NCL, we illustrate differences between subtypes in their presenting symptoms and clinical, imaging, and electrophysiological results to rai
Autor:
Marie-Odile Greneche, Catherine Delanoë, Samia Pichard, Laurent François, Silvana de Lucia, Manuel Schiff, Stéphane Auvin, Adina Ilea
Publikováno v:
European Journal of Paediatric Neurology. 20:674-677
The ketogenic diet is an evidence-based treatment for resistant epilepsy including Lennox-Gastaut syndrome. This diet is based on low carbohydrate-high fat intakes. Dietary treatment is also therapeutic for inborn errors of metabolism such as aminoac
Autor:
Catherine Delanoë, Stéphane Auvin, Vanina Bellavoine, Marie-Odile Greneche, Domitille Gras, Sofiane Amalou, Adina Ilea, Laurent François
Publikováno v:
Developmental medicine and child neurology. 58(11)
Aim Glucose transporter type 1 deficiency syndrome (GLUT1-DS) results from impaired glucose transport into the brain, and is treated with a ketogenic diet. A few reports have suggested effectiveness of treatment using the modified Atkins diet (MAD).