Individualized prediction of seizure relapse and outcomes following antiepileptic drug withdrawal after pediatric epilepsy surgery
Lamberink, Herm J., Boshuisen, Kim, Otte, Willem M., Geleijns, Karin, Braun, Kees P. J., Feucht, M, Gröppel, G, Kahane, P, Minotti, L, Arzimanoglou, A, Ryvlin, P, Panagiotakaki, E, Bellescize, J, Ostrowsky‐Coste, K, Hirsch, E, Valenti, M, Polster, T, Sassen, R, Hoppe, C, Kuczaty, S, Elger, C, Schubert, S, Strobl, K, Bast, T, Barba, C, Guerrini, R, Giordano, F, Francione, S, Caputo, D, Boshuisen, K, Braun, K P J, Uiterwaal, C S P M, Nieuwenhuizen, O, Leijten, F S, Rijen, P C, Seeck, M, Yalnizoglu, D, Turanli, G, Topcu, M, Özkara, C, Uzan, M, Cross, J H, D'Argenzio, L, Harkness, W
Published in Epilepsia (Copenhagen) (01.03.2018)
Published in Epilepsia (Copenhagen) (01.03.2018)
Get full text
Journal Article
Neuropsychological and behavioral disorders screening program in new-onset childhood epilepsies. Preliminary results using child behavior checklist evaluation
Ilski Lecoanet, F, Gavanon, M, Abadie, R, Laurent, A, Herbillon, V, Panagiotakaki, E, Bellescize, J.D.E, Keo kosal, P, Ostrowsky-Coste, K, Montavont, A, Arzimanoglou, A
Published in European journal of paediatric neurology (01.06.2017)
Published in European journal of paediatric neurology (01.06.2017)
Get full text
Journal Article
RUFIPRAT: A retrospective study on the everyday clinical use of Rufinamide in children with refractory epilepsy
Milleret, C, Losito, E, Auvin, S, Di Meglio, C, Cances, C, Dubois, F, Doudoux, H, Nabbout, R, Milh, M, Verceuil, L, Gokce-Samar, Z, Panagiotakaki, E, Arzimanoglou, A
Published in European journal of paediatric neurology (01.06.2017)
Published in European journal of paediatric neurology (01.06.2017)
Get full text
Journal Article
ATP1A3 screening in patients with alternating hemiplegia of childhood and related phenotypes
Panagiotakaki, E, Michel, J, Doummar, D, Mignot, C, Flamand-Roze, E, Nicole, S, Guilbert, H, Sabouraud, P, Sanlaville, D, Arzimanoglou, A, Lesca, G
Published in European journal of paediatric neurology (01.06.2017)
Published in European journal of paediatric neurology (01.06.2017)
Get full text
Journal Article
Effects of regular auditory or auditory-visual prime sequence on the syntax treatment in childhood absence epilepsy
Gavanon, M, Abadie, R, Ilski Lecoanet, F, Tiillmann, B, Panagiotakaki, E, De Bellescize, J, Keo Kosal, P, Ostrowsky-Coste, K, Montavont, A, Arzimanoglou, A, Bedoin, N
Published in European journal of paediatric neurology (01.06.2017)
Published in European journal of paediatric neurology (01.06.2017)
Get full text
Journal Article
Next-generation sequencing allows a diagnostic yield of 23.7% in monogenic epilepsies
Lesca, G, Labalme, A, Mignot, C, Chatron, N, Van de Velde Boermans, L, des Portes, V, Bogoin, J, Ville, D, de Belescize, J, Nougues, M.C, Doummar, D, Afenjar, A, Poulat, A.L, Panagiotakaki, E, Valence, S, Arzimanoglou, A, Heron, D, Leguern, E, Sanlaville, D, Nava, C
Published in European journal of paediatric neurology (01.06.2017)
Published in European journal of paediatric neurology (01.06.2017)
Get full text
Journal Article
Absence of mutation in the SLC2A1 gene in a cohort of patients with alternating hemiplegia of childhood (AHC)
Vuillaumier-Barrot, S, Panagiotakaki, E, Le Bizec, C, El Baba, C, Fontaine, B, Arzimanoglou, A, Seta, N, Nicole, S
Published in Neuropediatrics (01.12.2010)
Published in Neuropediatrics (01.12.2010)
Get more information
Journal Article
No Mutation in the SLC2A3 Gene in Cohorts of GLUT1 Deficiency Syndrome–Like Patients Negative for SLC2A1 and in Patients with AHC Negative for ATP1A3
Bizec, C. Le, Nicole, S., Panagiotakaki, E., Seta, N., Vuillaumier-Barrot, S.
Published in JIMD Reports - Volume 12 (01.01.2014)
Published in JIMD Reports - Volume 12 (01.01.2014)
Get full text
Book Chapter
Journal Article
Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients
Panagiotakaki, Eleni, De Grandis, Elisa, Stagnaro, Michela, Heinzen, Erin L, Fons, Carmen, Sisodiya, Sanjay, de Vries, Boukje, Goubau, Christophe, Weckhuysen, Sarah, Kemlink, David, Scheffer, Ingrid, Lesca, Gaëtan, Rabilloud, Muriel, Klich, Amna, Ramirez-Camacho, Alia, Ulate-Campos, Adriana, Campistol, Jaume, Giannotta, Melania, Moutard, Marie-Laure, Doummar, Diane, Hubsch-Bonneaud, Cecile, Jaffer, Fatima, Cross, Helen, Gurrieri, Fiorella, Tiziano, Danilo, Nevsimalova, Sona, Nicole, Sophie, Neville, Brian, van den Maagdenberg, Arn M J M, Mikati, Mohamad, Goldstein, David B, Vavassori, Rosaria, Arzimanoglou, Alexis
Published in Orphanet journal of rare diseases (26.09.2015)
Published in Orphanet journal of rare diseases (26.09.2015)
Get full text
Journal Article
White matter development in children with benign childhood epilepsy with centro-temporal spikes
CIUMAS, Carolina, SAIGNAVONGS, Mani, MARINIER, Dominique Sappey, MONTAVONT, Alexandra, OSTROWSKY-COSTE, Karine, BEDOIN, Nathalie, RYVLIN, Philippe, LLSKI, Faustine, HERBILLON, Vania, LAURENT, Agathe, LOTHE, Amelie, HECKEMANN, Rolf A, DE BELLESCIZE, Julitta, PANAGIOTAKAKI, Eleni, HANNOUN, Salem
Published in Brain (London, England : 1878) (01.04.2014)
Published in Brain (London, England : 1878) (01.04.2014)
Get full text
Journal Article
Intelligence quotient improves after antiepileptic drug withdrawal following pediatric epilepsy surgery
Boshuisen, Kim, van Schooneveld, Monique M. J., Uiterwaal, Cuno S. P. M., Cross, J. Helen, Harrison, Sue, Polster, Tilman, Daehn, Marion, Djimjadi, Sarina, Yalnizoglu, Dilek, Turanli, Guzide, Sassen, Robert, Hoppe, Christian, Kuczaty, Stefan, Barba, Carmen, Kahane, Philippe, Schubert-Bast, Susanne, Reuner, Gitta, Bast, Thomas, Strobl, Karl, Mayer, Hans, de Saint-Martin, Anne, Seegmuller, Caroline, Laurent, Agathe, Arzimanoglou, Alexis, Braun, Kees P. J.
Published in Annals of neurology (01.07.2015)
Published in Annals of neurology (01.07.2015)
Get full text
Journal Article
ALG3-CDG: Report of two siblings with antenatal features carrying homozygous p.Gly96Arg mutation
Lepais, Laureline, Cheillan, David, Frachon, Sophie Collardeau, Hays, Stéphane, Matthijs, Gert, Panagiotakaki, Eleni, Abel, Carine, Edery, Patrick, Rossi, Massimiliano
Published in American journal of medical genetics. Part A (01.11.2015)
Published in American journal of medical genetics. Part A (01.11.2015)
Get full text
Journal Article
O59 – 1906 Alternating hemiplegia and ATP1A3 gene: evolution of 12 cases into adulthood. Genotype-Phenotype correlations
Ramirez-Camacho, A, Panagiotakaki, E, Poncelin, D, Nicole, S, Lesca, G, Arzimanoglou, A
Published in European journal of paediatric neurology (01.09.2013)
Published in European journal of paediatric neurology (01.09.2013)
Get full text
Journal Article
A survey of the European Reference Network EpiCARE on clinical practice for selected rare epilepsies
Baumgartner, Tobias, Carreño, Mar, Rocamora, Rodrigo, Bisulli, Francesca, Boni, Antonella, Brázdil, Milan, Horak, Ondrej, Craiu, Dana, Pereira, Cristina, Guerrini, Renzo, San Antonio‐Arce, Victoria, Schulze‐Bonhage, Andreas, Zuberi, Sameer M., Hallböök, Tove, Kalviainen, Reetta, Lagae, Lieven, Nguyen, Sylvie, Quintas, Sofia, Franco, Ana, Cross, J. Helen, Walker, Matthew, Arzimanoglou, Alexis, Rheims, Sylvain, Granata, Tiziana, Canafoglia, Laura, Johannessen Landmark, Cecilie, Sen, Arjune, Rattihalli, Rohini, Nabbout, Rima, Tartara, Elena, Santos, Manuela, Rangel, Rui, Krsek, Pavel, Marusic, Petr, Specchio, Nicola, Braun, Kees P. J., Smeyers, Patricia, Villanueva, Vicente, Kotulska, Katarzyna, Surges, Rainer, Tinuper, Paolo, Licchetta, Laura, Michelucci, Roberto, Toulouse, Joseph, Panagiotakaki, Eleni, Ostrowsky‐Coste, Karine, Lesca, Gaetan, de Curtis, Marco, Elisak, Martin, Domańska‐Pakiea, Dorota, Sadowski, Krzysztof
Published in Epilepsia open (01.03.2021)
Published in Epilepsia open (01.03.2021)
Get full text
Journal Article
Genotype-phenotype correlations for a wide spectrum of mutations in the Wilson disease gene (ATP7B)
Panagiotakaki, Eleni, Tzetis, Maria, Manolaki, Nina, Loudianos, Giorgos, Papatheodorou, Athanasios, Manesis, Emmanuel, Nousia-Arvanitakis, Sanda, V, Syriopoulou, Kanavakis, Emmanuel
Published in American journal of medical genetics. Part A (01.12.2004)
Published in American journal of medical genetics. Part A (01.12.2004)
Get full text
Journal Article
Hémiplégie alternante et gène ATP1A3 : quelle évolution à l’âge adulte ? À propos de 12 observations
Panagiotakaki, E., Poncelin, D., Nicole, S., Lesca, G., Arzimanoglou, A.
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.04.2013)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.04.2013)
Get full text
Journal Article
659 Wilson's disease in children: A 22-year experience
Manolaki, N., Nikolopoulou, G., Daikos, G., Panagiotakaki, E., Tzetis, M., Kanavakis, E., Syriopoulou, V.
Published in Journal of hepatology (01.04.2006)
Published in Journal of hepatology (01.04.2006)
Get full text
Journal Article
Delineation of the spectrum of Wilson disease mutations in the Greek population and the identification of six novel mutations
Loudianos, G, Lovicu, M, Solinas, P, Kanavakis, E, Tzetis, M, Manolaki, N, Panagiotakaki, E, Karpathios, T, Cao, A
Published in Genetic testing (2000)
Published in Genetic testing (2000)
Get more information
Journal Article