Guido Rubboli

Guido Rubboli

Clinical Professor

Member of:

    ORCID: 0000-0002-5309-2514

    Publication year:
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    1 - 10 out of 12Page size: 10
    1. 2022
    2. Published

      Answer to: Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy (Amadori E et al., 2022). EJMG-D-22-00384

      Amadori, E., Pellino, G., Bansal, L., Mazzone, S., Møller, R. S., Rubboli, Guido, Striano, P. & Russo, A., 2022, In: European Journal of Medical Genetics. 65, 12, 104634.

      Research output: Contribution to journal › Comment/debate › Research › peer-review

    3. Published

      Automated ictal EEG source imaging: A retrospective, blinded clinical validation study

      Baroumand, A. G., Arbune, A. A., Strobbe, G., Keereman, V., Pinborg, Lars Hageman, Fabricius, M., Rubboli, Guido, Gøbel Madsen, C., Jespersen, B., Brennum, J., Mølby Henriksen, O., Mierlo, P. V. & Beniczky, S., 2022, In: Clinical Neurophysiology. 141, p. 119-125

      Research output: Contribution to journal › Journal article › Research › peer-review

    4. Published

      Epilepsy in neurodegenerative diseases

      Neri, S., Mastroianni, G., Gardella, E., Aguglia, U. & Rubboli, Guido, 2022, In: Epileptic Disorders. 24, 2, p. 249-273 25 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    5. Published

      Expanding the phenotype of PURA-related developmental epileptic encephalopathy

      Rubboli, Guido & Johannesen, K. M., 2022, In: Epileptic Disorders. 24, 2, p. 445-446 2 p.

      Research output: Contribution to journal › Comment/debate › Research › peer-review

    6. Published

      Functional Effects of Epilepsy Associated KCNT1 Mutations Suggest Pathogenesis via Aberrant Inhibitory Neuronal Activity

      Rychkov, G. Y., Shaukat, Z., Lim, C. X., Hussain, R., Roberts, B. J., Bonardi, C. M., Rubboli, Guido, Meaney, B. F., Whitney, R., Møller, R. S., Ricos, M. G. & Dibbens, L. M., 2022, In: International Journal of Molecular Sciences. 23, 23, 15133.

      Research output: Contribution to journal › Journal article › Research › peer-review

    7. Published

      Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy

      Amadori, E., Pellino, G., Bansal, L., Mazzone, S., Møller, R. S., Rubboli, Guido, Striano, P. & Russo, A., 2022, In: European Journal of Medical Genetics. 65, 4, 104450.

      Research output: Contribution to journal › Review › Research › peer-review

    8. Published

      Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications

      Johannesen, K. M., Liu, Y., Koko, M., Gjerulfsen, C. E., Sonnenberg, L., Schubert, J., Fenger, C. D., Eltokhi, A., Rannap, M., Koch, N. A., Lauxmann, S., Krüger, J., Kegele, J., Canafoglia, L., Franceschetti, S., Mayer, T., Rebstock, J., Zacher, P., Ruf, S., Alber, M. & 109 others, Sterbova, K., Lassuthová, P., Vlckova, M., Lemke, J. R., Platzer, K., Krey, I., Heine, C., Wieczorek, D., Kroell-Seger, J., Lund, C., Klein, K. M., Au, P. Y. B., Rho, J. M., Ho, A. W., Masnada, S., Veggiotti, P., Giordano, L., Accorsi, P., Høi-Hansen, Christina Engel, Striano, P., Zara, F., Verhelst, H., Verhoeven, J. S., Braakman, H. M. H., van der Zwaag, B., Harder, A. V. E., Brilstra, E., Pendziwiat, M., Lebon, S., Vaccarezza, M., Le, N. M., Christensen, J., Grønborg, S., Scherer, S. W., Howe, J., Fazeli, W., Howell, K. B., Leventer, R., Stutterd, C., Walsh, S., Gerard, M., Gerard, B., Matricardi, S., Bonardi, C. M., Sartori, S., Berger, A., Hoffman-Zacharska, D., Mastrangelo, M., Darra, F., Vøllo, A., Motazacker, M. M., Lakeman, P., Nizon, M., Betzler, C., Altuzarra, C., Caume, R., Roubertie, A., Gélisse, P., Marini, C., Guerrini, R., Bilan, F., Tibussek, D., Koch-Hogrebe, M., Perry, M. S., Ichikawa, S., Dadali, E., Sharkov, A., Mishina, I., Abramov, M., Kanivets, I., Korostelev, S., Kutsev, S., Wain, K. E., Eisenhauer, N., Wagner, M., Savatt, J. M., Müller-Schlüter, K., Bassan, H., Borovikov, A., Nassogne, M. C., Destrée, A., Schoonjans, A. S., Meuwissen, M., Buzatu, M., Jansen, A., Scalais, E., Srivastava, S., Tan, W. H., Olson, H. E., Loddenkemper, T., Poduri, A., Helbig, K. L., Helbig, I., Fitzgerald, M. P., Goldberg, E. M., Roser, T., Borggraefe, I., Brünger, T., May, P., Lal, D., Lederer, D., Rubboli, Guido, Heyne, H. O., Lesca, G., Hedrich, U. B. S., Benda, J., Gardella, E., Lerche, H. & Møller, R. S., 2022, In: Brain. 145, 9, p. 2991-3009 19 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    9. Published

      Impact of Genetic Testing on Therapeutic Decision-Making in Childhood-Onset Epilepsies - a Study in a Tertiary Epilepsy Center

      Bayat, A., Fenger, C. D., Techlo, T. R., Højte, A. F., Nørgaard, I., Hansen, Thomas Folkmann, Rubboli, Guido, Møller, R. S. & group, D. C. C. R. S., 2022, In: Neurotherapeutics. 19, p. 1353–1367

      Research output: Contribution to journal › Journal article › Research › peer-review

    10. Published

      Pseudoresistance in idiopathic/genetic generalized epilepsies – Definitions, risk factors, and outcome

      Gesche, J., Cornwall, C. D., Delcomyn, L., Rubboli, Guido & Beier, C. P., 2022, In: Epilepsy and Behavior. 130, 108633.

      Research output: Contribution to journal › Journal article › Research › peer-review

    11. Published

      Sex-specific disease modifiers in juvenile myoclonic epilepsy

      Shakeshaft, A., Panjwani, N., Collingwood, A., Crudgington, H., Hall, A., Andrade, D. M., Beier, C. P., Fong, C. Y., Gardella, E., Gesche, J., Greenberg, D. A., Hamandi, K., Koht, J., Lim, K. S., Møller, R. S., Ng, C. C., Orsini, A., Rees, M. I., Rubboli, G., Selmer, K. K. & 7 others, Striano, P., Syvertsen, M., Thomas, R. H., Zarubova, J., Richardson, M. P., Strug, L. J. & Pal, D. K., 2022, In: Scientific Reports. 12, 1, 12 p., 2785.

      Research output: Contribution to journal › Journal article › Research › peer-review

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    ID: 119733516