Research

Epilepsy and movement disorders in Pediatrics

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Publications

  • Panagiotakaki, Eleni, Tiziano, Francesco D., Mikati, Mohamad A., Vijfhuizen, Lisanne S., Nicole, Sophie, Lesca, Gaetan, Abiusi, Emanuela, Novelli, Agnese, Di Pietro, Lorena, Harder, Aster V. E., Walley, Nicole M., De Grandis, Elisa, Poulat, Anne-Lise, Portes, Vincent Des, Lepine, Anne, Nassogne, Marie-Cecile, Arzimanoglou A, Vavassori, Rosaria, Koenderink, Jan, Thompson, Christopher H., George, Alfred L., Gurrieri, Fiorella, van den Maagdenberg, Arn M. J. M. and Heinzen, Erin L..

    Exome sequencing of ATP1A3 negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene

    EUROPEAN JOURNAL OF HUMAN GENETICS . : . Number of citations: 1

    [doi:10.1038/s41431-023-01489-4]

  • Nou-Fontanet L, Martín-Gómez C, Isabel-Gómez R, Bachoud-Lévi AC, Zorzi G, Capuano A, Blasco-Amaro JA and Ortigoza-Escobar JD.

    Systematic review of drug therapy for chorea in NXK2-1-related disorders: Efficacy and safety evidence from case studies and series.

    EUROPEAN JOURNAL OF NEUROLOGY . 30(12): 3928-3948.

    [doi:10.1111/ene.16038]

  • Lyu, Hang, Bosselmann, Christian M., Johannesen, Katrine M., Koko, Mahmoud, Ortigoza-Escobar JD, Aguilera-Albesa, Sergio, Nunez, Deyanira Garcia -Navas, Linnankivi, Tarja, Gaily, Eija, Ruiten, Henriette J. A. van, Richardson, Ruth, Betzler, Cornelia, Horvath, Gabriella, Brilstra, Eva, Geerdink, Niels, Orsucci, Daniele, Tessa, Alessandra, Gardella, Elena, Fleszar, Zofia, Schoels, Ludger, Lerche, Holger, Moller, Rikke S. and Liu, Yuanyuan.

    Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia

    EBioMedicine . 98: .

    [doi:10.1016/j.ebiom.2023.104855]

  • Auvin, Stephane, Arzimanoglou A, Beller, Cynthia, Floricel, Florin, Daniels, Tony and Bozorg, Ali.

    Safety, tolerability, and efficacy of adjunctive lacosamide in pediatric patients with epilepsy syndromes associated with generalized seizures: Phase 2, open-label exploratory trial

    Epilepsia . 64(11): 2947-2957.

    [doi:10.1111/epi.17741]

  • Limpo, Hiria, Candela-Cantó SA, Asensio, Silvia, Palacio-Navarro, Andrea, Aparicio J, Perin, Alejandra Climent, Hinojosa, Jose and Rumia, Jordi.

    A multidisciplinary approach to posterior quadrant disconnective epilepsy surgery in pediatric patients

    Neurochirurgie . 69(6): . Number of citations: 1

    [doi:10.1016/j.neuchi.2023.101489]

  • Muñoz-Pujol G, Ugarteburu O, Segur-Bailach E, Moliner S, Jurado S, Garrabou G, Guitart-Mampel M, García-Villoria J, Artuch-Iriberri R, Fons-Estupina C, Ribes A and Tort F.

    CRISPR/Cas9-based functional genomics strategy to decipher the pathogenicity of genetic variants in inherited metabolic disorders

    JOURNAL OF INHERITED METABOLIC DISEASE . 46(6): 1029-1042.

    [doi:10.1002/jimd.12681]

  • de Pedro Baena S, Sariego Jamardo A, Castro P, López González FJ, Sánchez Carpintero R, Cerisola A, Troncoso M, Witting S, Barrios A, Fons-Estupina C, López Pisón J and Ortigoza-Escobar JD.

    Exploring the Spectrum of RHOBTB2 Variants Associated with Developmental Encephalopathy 64: A Case Series and Literature Review

    Movement Disorders Clinical Practice . 10(11): 1671-1679.

    [doi:10.1002/mdc3.13880]

  • Mancuso, Michelangelo, Lopriore, Piervito, Lamperti, Costanza, Klopstock, Thomas, Rahman, Shamima, Licchetta, Laura, Kornblum, Cornelia, Wortmann, Saskia B., Dollfus, Helene, Papadopoulou, Maria T., Arzimanoglou A, Scarpa, Maurizio, Graessner, Holm and Evangelista, Teresinha.

    Current management of primary mitochondrial disorders in EU countries: the European Reference Networks survey

    JOURNAL OF NEUROLOGY . : .

    [doi:10.1007/s00415-023-12017-1]

  • Patel, Shital H., Panagiotakaki, Eleni, Papadopoulou, Maria T., Fons-Estupina C, De Grandis, Elisa, Vezyroglou, Aikaterini, Balestrini, Simona, Hong, Hwanhee, Liu, Beiyu, Prange, Lyndsey, Arzimanoglou A, Vavassori, Rosaria and Mikati, Mohamad A..

    Methodology of a Natural History Study of a Rare Neurodevelopmental Disorder: Alternating Hemiplegia of Childhood as a Prototype Disease

    JOURNAL OF CHILD NEUROLOGY . 38(10-12): 597-610. Number of citations: 2

    [doi:10.1177/08830738231197861]

  • Schluter, Agatha, Velez-Santamaria, Valentina, Verdura, Edgard, Rodriguez-Palmero, Agusti, Ruiz, Montserrat, Fourcade, Stephane, Planas-Serra, Laura, Launay, Nathalie, Guilera, Cristina, Martinez, Juan Jose, Homedes-Pedret, Christian, Alberti-Aguilo, M. Antonia, Zulaika, Miren, Marti, Itxaso, Troncoso, Monica, Tomas-Vila, Miguel, Bullich, Gemma, Garcia-Perez, M. Asuncion, Sobrido-Gomez, Maria-Jesus, Lopez-Laso, Eduardo, Fons-Estupina C, Del Toro, Mireia, Macaya, Alfons, Beltran, Sergi, Gutierrez-Solana, Luis G., Perez-Jurado, Luis A., Aguilera-Albesa, Sergio, de Munain, Adolfo Lopez, Casasnovas, Carlos, Pujol, Aurora and HSP Ataxia Workgrp.

    ClinPrior: an algorithm for diagnosis and novel gene discovery by network-based prioritization

    GENOME MEDICINE . 15(1): .

    [doi:10.1186/s13073-023-01214-2]