Personas / Equipo Humano

Alexis Arzimanoglou

Buscador de publicaciones

Publicaciones

  • Tchaicha S, Auvin S, Beniczky S, Brunklaus A, Lagae L, Perucca E, Surges R, Adler S, Helmstaedter C, Jansen F, Rubboli G, Ryvlin P, Specchio N, Trinka E, Blümcke I, de Giorgis V, Kotulska K, Lesca G, Malenica M, McTague A, Nabbout R, Møller RS, Arrieta SS, Brambilla I, Kosla M, Braun K, Cross JH and Arzimanoglou A.

    Areas of research priorities in epilepsy: A position paper of the European Reference Network for Rare and Complex Epilepsies, EpiCARE.

    Epilepsia Open . : .

    [doi:10.1002/epi4.70210]

  • Masnada S, De Giorgis V, Carugo U, Bahi-Buisson N, Cavallin M, Corbett M, Formica M, Gecz J, Petros N, Perucca E, Pichiecchio A, Fusar Poli P, Sherr EH, Van den Veyver IB, Zara F, Geroldinger M, Veggiotti P and Arzimanoglou A.

    Refining Aicardi Syndrome diagnostic Criteria: an expert-based consensus using a modified Delphi approach

    EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY . 60: 58-70.

    [doi:10.1016/j.ejpn.2025.11.004]

  • Nou-Fontanet L, Musokhranova U, Ramírez-Camacho A, Delgadillo V, Insuga VS, Fernández LA, Alonso-Colmenero I, Arzimanoglou A, Garcia-Cazorla A, De Oyarzabal-Sanz AL and Fons-Estupina C.

    AFG2A-related encephalopathy: Effectiveness of ketogenic diet in epilepsy and mitochondrial dynamics modulation

    EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY . 58: 20-26. Nº de citas: 1

    [doi:10.1016/j.ejpn.2025.07.007]

  • Lersch, R, Hartlieb, T, Pieper, T, Kudernatsch, M, Hofer, W, Barba, C, Guerrini, R, Giordano, F, Pommella, M, Schubert-Bast, S, Syrbe, S, Rego, R, Pinheiro, J, Feucht, M, Beck, A, Coras, R, Blumcke, I, Alber, M, Tacke, M, Rémi, J, Vollmar, C, Kunz, M, Shetty, J, Mclellan, A, Sokol, D, Kandasamy, J, Klotz, KA, San Antonio-Arce, V, Schulze-Bonhage, A, Pepper, J, Lo, WB, Arzimanoglou A, Francione, S, Braun, CJ and Borggraefe, I.

    Seizure outcomes following epilepsy surgery in pediatric and young adult patients with high-grade brain tumors: Results from a European survey

    EPILEPSIA . 66(6): 1865-1875. Nº de citas: 1

    [doi:10.1111/epi.18323]

  • Ghasemi, MR, Fateh, ST, Ben-Mahmoud, A, Gupta, V, Stühn, LG, Lesca, G, Chatron, N, Platzer, K, Edery, P, Sadeghi, H, Isidor, B, Cogné, B, Schulz, HL, Krauspe-Stübecke, I, Periyasamy, R, Nampoothiri, S, Mirfakhraie, R, Alijanpour, S, Syrbe, S, Pfeifer, U, Spranger, S, Grundmann-Hauser, K, Haack, TB, Papadopoulou, MT, Gonçalves, TD, Panagiotakaki, E, Arzimanoglou A, Tonekaboni, SH, Rossi, M, Korenke, GC, Lacassie, Y, Jang, MH, Layman, LC, Miryounesi, M and Kim, HG.

    Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of CNKSR2 in the Houge Type of X-Linked Syndromic Intellectual Development Disorder (MRXSHG)

    AMERICAN JOURNAL OF MEDICAL GENETICS PART A . 197(5): .

    [doi:10.1002/ajmg.a.63963]

  • Adler, S, D'Arco, F, Mankad, K, Kyncl, M, Arzimanoglou A and Marusic, P.

    Harmonization of MRI sequences across ERN EpiCARE centers

    Epilepsia Open . 10(2): 587-592. Nº de citas: 1

    [doi:10.1002/epi4.13115]

  • Moya Quiros V, Adham A, Convers P, Lesca G, Mauguiere F, Soulier H, Arzimanoglou A, Bayat A, Braakman H, Camdessanche JP, Casenave P, Chaton L, Chaix Y, Chochoi M, Depienne C, Desportes V, De Ridder J, Dinkelacker V, Gardella E, Kluger GJ, Jung J, Lemesle Martin M, Mancardi MM, Mueller M, Poulat AL, Platzer K, Roubertie A, Stokman MF, Vulto-van Silfhout AT, Wiegand G and Mazzola L.

    Electro-Clinical Features and Functional Connectivity Analysis in SYN1-Related Epilepsy

    ANNALS OF NEUROLOGY . 97(1): 34-50. Nº de citas: 1

    [doi:10.1002/ana.27063]

  • Specchio N, Trivisano M, Aronica E, Balestrini S, Arzimanoglou A, Colasante G, Cross JH, Jozwiak S, Wilmshurst JM, Vigevano F, Auvin S, Nabbout R and Curatolo P.

    The expanding field of genetic developmental and epileptic encephalopathies: current understanding and future perspectives

    Lancet Child & Adolescent Health . 8(11): 821-834. Nº de citas: 17

    [doi:10.1016/S2352-4642(24)00196-2]

  • Amin, S, Moller, RS, Aledo-Serrano, A, Arzimanoglou A, Bager, P, Józwiak, S, Kluger, GJ, López-Cabeza, S, Nabbout, R, Partridge, CA, Schubert-Bast, S, Specchio, N and Kälviäinen, R.

    Providing quality care for people with CDKL5 deficiency disorder: A European expert panel opinion on the patient journey

    Epilepsia Open . 9(3): 832-849. Nº de citas: 4

    [doi:10.1002/epi4.12914]

  • Papadopoulou MT, Muccioli L, Bisulli F, Klotz KA, Fons-Estupina C, Trivisano M, Kabulashvili T, Specchio N, Lesca G and Arzimanoglou A.

    Accessibility, availability and common practices regarding genetic testing for epilepsy across Europe: A survey of the European Reference Network EpiCARE

    Epilepsia Open . 9(3): 996-1006. Nº de citas: 5

    [doi:10.1002/epi4.12930]