Items where Author is "Striano, Pasquale"

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Journal Article

Johannesen, Katrine M. and Gardella, Elena and Encinas, Alejandra C. and Lehesjoki, Anna‐Elina and Linnankivi, Tarja and Petersen, Michael B. and Lund, Ida C. B. and Blichfeldt, Susanne and Miranda, Maria J. and Pal, Deb K. and Lascelles, Karine and Procopis, Peter and Orsini, Alessandro and Bonuccelli, Alice and Giacomini, Thea and Helbig, Ingo and Fenger, Christina D. and Sisodiya, Sanjay M. and Hernandez‐Hernandez, Laura and Krithika, S. and Rumple, Melissa and Masnada, Silvia and Valente, Marialuisa and Cereda, Cristina and Giordano, Lucio and Accorsi, Patrizia and Bürki, Sarah E. and Mancardi, Margherita and Korff, Christian and Guerrini, Renzo and Spiczak, Sarah and Hoffman‐Zacharska, Dorota and Mazurczak, Tomasz and Coppola, Antonietta and Buono, Salvatore and Vecchi, Marilena and Hammer, Michael F. and Varesio, Costanza and Veggiotti, Pierangelo and Lal, Dennis and Brünger, Tobias and Zara, Federico and Striano, Pasquale and Rubboli, Guido and Møller, Rikke S. (2019) The spectrum of intermediate SCN 8A ‐related epilepsy. Epilepsia, 60 (5). pp. 830-844. ISSN 1528-1167

Baldassari, Sara and Picard, Fabienne and Verbeek, Nienke E. and van Kempen, Marjan and Brilstra, Eva H. and Lesca, Gaetan and Conti, Valerio and Guerrini, Renzo and Bisulli, Francesca and Licchetta, Laura and Pippucci, Tommaso and Tinuper, Paolo and Hirsch, Edouard and de Saint Martin, Anne and Chelly, Jamel and Rudolf, Gabrielle and Chipaux, Mathilde and Ferrand-Sorbets, Sarah and Dorfmüller, Georg and Sisodiya, Sanjay and Balestrini, Simona and Schoeler, Natasha and Hernandez-Hernandez, Laura and Krithika, S. and Oegema, Renske and Hagebeuk, Eveline and Gunning, Boudewijn and Deckers, Charles and Berghuis, Bianca and Wegner, Ilse and Niks, Erik and Jansen, Floor E. and Braun, Kees and de Jong, Daniëlle and Rubboli, Guido and Talvik, Inga and Sander, Valentin and Uldall, Peter and Jacquemont, Marie-Line and Nava, Caroline and Leguern, Eric and Julia, Sophie and Gambardella, Antonio and d’Orsi, Giuseppe and Crichiutti, Giovanni and Faivre, Laurence and Darmency, Veronique and Benova, Barbora and Krsek, Pavel and Biraben, Arnaud and Lebre, Anne-Sophie and Jennesson, Mélanie and Sattar, Shifteh and Marchal, Cécile and Nordli, Douglas R. and Lindstrom, Kristin and Striano, Pasquale and Lomax, Lysa B. and Kiss, Courtney and Bartolomei, Fabrice and Lepine, Anne F. and Schoonjans, An-Sofie and Stouffs, Katrien and Jansen, Anna and Panagiotakaki, Eleni and Ricard-Mousnier, Brigitte and Thevenon, Julien and de Bellescize, Julitta and Catenoix, Hélène and Dorn, Thomas and Zenker, Martin and Müller-Schlüter, Karen and Brandt, Christian and Krey, Ilona and Polster, Tilman and Wolff, Markus and Balci, Meral and Rostasy, Kevin and Achaz, Guillaume and Zacher, Pia and Becher, Thomas and Cloppenborg, Thomas and Yuskaitis, Christopher J. and Weckhuysen, Sarah and Poduri, Annapurna and Lemke, Johannes R. and Møller, Rikke S. and Baulac, Stéphanie (2019) The landscape of epilepsy-related GATOR1 variants. Genetics in Medicine, 21 (2). pp. 398-408. ISSN 1530-0366

Zagaglia, Sara and Selch, Christina and Nisevic, Jelena R. and Mei, Davide and Michalak, Zuzanna and Hernandez-Hernandez, Laura and Krithika, S. and Vezyroglou, Katharina and Varadkar, Sophia M. and Pepler, Alexander and Biskup, Saskia and Leão, Miguel and Gärtner, Jutta and Merkenschlager, Andreas and Jaksch, Michaela and Møller, Rikke S. and Gardella, Elena and Kristiansen, Britta S. and Hansen, Lars K. and Vari, Maria S. and Helbig, Katherine L. and Desai, Sonal and Smith-Hicks, Constance L. and Hino-Fukuyo, Naomi and Talvik, Tiina and Laugesaar, Rael and Ilves, Pilvi and Õunap, Katrin and Körber, Ingrid and Hartlieb, Till and Kudernatsch, Manfred and Winkler, Peter and Schimmel, Mareike and Hasse, Anette and Knuf, Markus and Heinemeyer, Jan and Makowski, Christine and Ghedia, Sondhya and Subramanian, Gopinath M. and Striano, Pasquale and Thomas, Rhys H. and Micallef, Caroline and Thom, Maria and Werring, David J. and Kluger, Gerhard J. and Cross, J. Helen and Guerrini, Renzo and Balestrini, Simona and Sisodiya, Sanjay M. (2018) Neurologic phenotypes associated with COL4A1/2 mutations. Neurology, 91 (22). e2078-e2088. ISSN 1526-632X

This list was generated on Wed Oct 28 02:22:30 2020 GMT.