Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Vanina Bellavoine"'
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:
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:
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
Difference in anxiety symptoms between children and their parents facing a first seizure or epilepsy
Autor:
Vanina Bellavoine, Pascal Dournaud, Stéphane Auvin, Dana Merdariu, Jessica Save-Pédebos, Estelle Goujon, Marion Danse
Publikováno v:
Epilepsy & Behavior. 31:97-101
Many studies have shown that anxiety disorders are common in children with epilepsy. We explored symptoms of anxiety simultaneously in children and their parents. We conducted a cross-sectional study using the Revised Children's Manifest Anxiety Scal
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).
Publikováno v:
Epilepsy & Behavior. 21:446-448
Objective The first seizure in Dravet syndrome is often considered a febrile seizure (FS), but shortly thereafter, both FSs and seizures without fever occur, leading to diagnosis. Fever remains a factor that easily precipitates seizures. We studied t
Autor:
Stéphane Auvin, Emilie Bourel, Adina Ilea, Vanina Bellavoine, Dana Merdariu, Maria Elisa Pires, Patrick Berquin
Publikováno v:
Epilepsy research. 105(1-2)
Summary Ketogenic diet (KD) is an efficient treatment for refractory epilepsy including infantile spasms (IS). We evaluated the effect of a KD to treat IS as a third-line treatment, after vigabatrin (VGB) and steroids. We evaluated the efficacy and t
Publikováno v:
Braindevelopment. 35(2)
The syndrome of malignant migrating partial seizures of infancy (MMPSI) is characterized by early onset of multiple seizure types and overall poor prognosis. Seizures are markedly drug resistant and few reports have suggested the efficacy of some ant
Autor:
Dana Merdariu, Odile Boespflug-Tanguy, Stéphane Auvin, Catherine Delanoë, Vanina Bellavoine, Monique Elmaleh-Bergès, Pierre Gressens
Publikováno v:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 16(5)
Hemiconvulsion–Hemiplegia (HH) syndrome is an uncommon consequence of prolonged focal febrile convulsive seizures in infancy and early childhood. It is characterized by the occurrence of prolonged clonic seizures with unilateral predominance occurr
P01.11 Parental perceptions of fever and fever management practices in children with Dravet Syndrome
Publikováno v:
European Journal of Paediatric Neurology. 15:S34-S35