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Kommentar/debat
2020

Reader response: SYNGAP1 encephalopathy: A distinctive generalized developmental and epileptic encephalopathy

Wolf, P., von Stülpnagel, C., Hartlieb, T., Møller, R. S. & Kluger, G. J., 25. feb. 2020, I : Neurology. 94, 8, s. 368-369

Publikation: Bidrag til tidsskriftKommentar/debatForskningpeer review

The impact of low-risk genetic variants in self-limited epilepsy with centrotemporal spikes aka Rolandic epilepsy

Hansen, T. F. & Møller, R. S., aug. 2020, I : EBioMedicine. 58, 102896.

Publikation: Bidrag til tidsskriftKommentar/debatForskningpeer review

Åben adgang
2019

Correction: IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients

Mignot, C., McMahon, A. C., Bar, C., Campeau, P. M., Davidson, C., Buratti, J., Nava, C., Jacquemont, M. L., Tallot, M., Milh, M., Edery, P., Marzin, P., Barcia, G., Barnerias, C., Besmond, C., Bienvenu, T., Bruel, A. L., Brunga, L., Ceulemans, B., Coubes, C. & 66 flere, Cristancho, A. G., Cunningham, F., Dehouck, M. B., Donner, E. J., Duban-Bedu, B., Dubourg, C., Gardella, E., Gauthier, J., Geneviève, D., Gobin-Limballe, S., Goldberg, E. M., Hagebeuk, E., Hamdan, F. F., Hančárová, M., Hubert, L., Ioos, C., Ichikawa, S., Janssens, S., Journel, H., Kaminska, A., Keren, B., Koopmans, M., Lacoste, C., Laššuthová, P., Lederer, D., Lehalle, D., Marjanovic, D., Métreau, J., Michaud, J. L., Miller, K., Minassian, B. A., Morales, J., Moutard, M. L., Munnich, A., Ortiz-Gonzalez, X. R., Pinard, J. M., Prchalová, D., Putoux, A., Quelin, C., Rosen, A. R., Roume, J., Rossignol, E., Simon, M. E. H., Smol, T., Shur, N., Shelihan, I., Štěrbová, K., Vyhnálková, E., Vilain, C., Soblet, J., Smits, G., Yang, S. P., van der Smagt, J. J., van Hasselt, P. M., van Kempen, M., Weckhuysen, S., Helbig, I., Villard, L., Héron, D., Koeleman, B., Møller, R. S., Lesca, G., Helbig, K. L., Nabbout, R., Verbeek, N. E. & Depienne, C., aug. 2019, I : Genetics in Medicine. 21, 8, s. 1897-1898

Publikation: Bidrag til tidsskriftKommentar/debatForskningpeer review

Åben adgang

Erratum: Correction: The landscape of epilepsy-related GATOR1 variants (Genetics in medicine : official journal of the American College of Medical Genetics (2019) 21 2 (398-408))

Baldassari, S., Picard, F., Verbeek, N. E., van Kempen, M., Brilstra, E. H., Lesca, G., Conti, V., Guerrini, R., Bisulli, F., Licchetta, L., Pippucci, T., Tinuper, P., Hirsch, E., de Saint Martin, A., Chelly, J., Rudolf, G., Chipaux, M., Ferrand-Sorbets, S., Dorfmüller, G., Sisodiya, S. & 68 flere, Balestrini, S., Schoeler, N., Hernandez-Hernandez, L., Krithika, S., Oegema, R., Hagebeuk, E., Gunning, B., Deckers, C., Berghuis, B., Wegner, I., Niks, E. H., Jansen, F. E., Braun, K., de Jong, D., Rubboli, G., Talvik, I., Sander, V., Uldall, P., Jacquemont, M. L., Nava, C., Leguern, E., Julia, S., Gambardella, A., d'Orsi, G., Crichiutti, G., Faivre, L., Darmency, V., Benova, B., Krsek, P., Biraben, A., Lebre, A. S., Jennesson, M., Sattar, S., Marchal, C., NordliJr, D. R., Lindstrom, K., Striano, P., Lomax, L. B., Kiss, C., Bartolomei, F., Lepine, A. F., Schoonjans, A. S., Stouffs, K., Jansen, A., Panagiotakaki, E., Ricard-Mousnier, B., Thevenon, J., de Bellescize, J., Catenoix, H., Dorn, T., Zenker, M., Müller-Schlüter, K., Brandt, C., Krey, I., Polster, T., Wolff, M., Balci, M., Rostasy, K., Achaz, G., Zacher, P., Becher, T., Cloppenborg, T., Yuskaitis, C. J., Weckhuysen, S., Poduri, A., Lemke, J. R., Møller, R. S. & Baulac, S., 1. aug. 2019, I : Genetics in medicine : official journal of the American College of Medical Genetics. 21, 8, s. 1896 1 s.

Publikation: Bidrag til tidsskriftKommentar/debatForskningpeer review

Åben adgang
2018

Antiepileptic effect of olanzapine in epilepsy patients with atypical depressive comorbidity

Qiu, X., Zingano, B., He, S., Zhu, X., Peng, A., Duan, J., Wolf, P. & Chen, L., 1. jun. 2018, I : Epileptic Disorders. 20, 3, s. 225-231

Publikation: Bidrag til tidsskriftKommentar/debatForskningpeer review

Corrigendum to “Increasing volume and complexity of pediatric epilepsy surgery with stable seizure outcome between 2008 and 2014: A nationwide multicenter study” [Epilepsy Behav. Oct 2017; 75C:151-157](S1525505017304961)(10.1016/j.yebeh.2017.08.010)

Barba, C., Specchio, N., Guerrini, R., Tassi, L., DeMasi, S., Cardinale, F., Pellacani, S., De Palma, L., Battaglia, D., Tamburrini, G., Didato, G., Freri, E., Consales, A., Nozza, P., Zamponi, N., Cesaroni, E., Di Gennaro, G., Esposito, V., Giulioni, M., Tinuper, P. & 7 flere, Colicchio, G., Rocchi, R., Rubboli, G., Giordano, F., Russo, G. L., Marras, C. E. & Cossu, M., mar. 2018, I : Epilepsy and Behavior. 80, s. 380 1 s.

Publikation: Bidrag til tidsskriftKommentar/debatForskningpeer review

Reply to “10-10 electrode system for EEG recording”

Seeck, M., Bast, T., Leijten, F., He, B. & Beniczky, S., maj 2018, I : Clinical Neurophysiology. 129, 5, s. 1104 1 s.

Publikation: Bidrag til tidsskriftKommentar/debatForskningpeer review

2017

A country fool's progress

Wolf, P., 2017, I : Epilepsy and Behavior. 74, s. 173-176

Publikation: Bidrag til tidsskriftKommentar/debatFormidling

Mitochondrial respiratory chain complex enzyme activities of limbic structures and psychiatric diagnosis in temporal lobe epilepsy patients: Preliminary results

Osório, C. M., Lin, K., Guarnieri, R., de Oliveira Thais, M. E. R., Dresch Vascouto, H., Remor, A. P., Lopes, M. W., Linhares, M. N., Ben, J., de Paula Martins, R., Hoeller, A. A., Wolf, P., Latini, A. & Walz, R., 2017, I : CNS Neuroscience & Therapeutics. 23, 8, s. 700-702

Publikation: Bidrag til tidsskriftKommentar/debatForskningpeer review

Salzburg criteria: can we extend validation to critical care? – Authors' reply

Leitinger, M., Trinka, E., Gardella, E., Kalss, G. & Beniczky, S., 2017, I : The Lancet Neurology. 16, 1, s. 25-26

Publikation: Bidrag til tidsskriftKommentar/debatForskningpeer review

The new ILAE seizure classification: 63 seizure types?

the SCORE consortium, 2017, I : Epilepsia. 58, 7, s. 1298-1300

Publikation: Bidrag til tidsskriftKommentar/debatForskningpeer review

2016

Letter to the editor: confirming neonatal seizure and late onset ataxia in SCN2A Ala263Val

Johannesen, K. M., Miranda, M. J., Lerche, H. & Møller, R. S., 2016, I : Journal of Neurology. 263, 7, s. 1459-1460

Publikation: Bidrag til tidsskriftKommentar/debatForskningpeer review

Reply: PKD_Not always nomina sunt consequentia rerum

Gardella, E., Beniczky, S., Møller, R. S., Becker, F., Lemke, J. R., Syrbe, S., Eiberg, H., Bast, T., Steinhoff, B., Nürnberg, P., Gellert, P., Dahl, H. A., Weckhuysen, S., Heron, S., Dibbens, L., Hjalgrim, H., Lerche, H. & Weber, Y. G., 21. apr. 2016, I : Annals of Neurology. 80, 1, s. 168-169

Publikation: Bidrag til tidsskriftKommentar/debatForskningpeer review