Items where Author is "Hernandez-Hernandez, Laura"

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Journal Article

Zagaglia, Sara and Steel, Dora and Krithika, S. and Hernandez-Hernandez, Laura and Custodio, Helena M. and Gorman, Kathleen M. and Vezyroglou, Aikaterini and Møller, Rikke S. and King, Mary D. and Hammer, Trine B. and Spaull, Robert and Fazeli, Walid and Bartolomaeus, Tobias and Doummar, Diane and Keren, Boris and Mignot, Cyril and Bednarek, Nathalie and Cross, J. Helen and Mallick, Andrew A. and Sanchis-Juan, Alba and Basu, Anna and Raymond, F. Lucy and Lynch, Bryan J. and Majumdar, Anirban and Stamberger, Hannah and Weckhuysen, Sarah and Sisodiya, Sanjay M. and Kurian, Manju A. (2021) RHOBTB2 mutations expand the phenotypic spectrum of alternating hemiplegia of childhood. Neurology. ISSN 1526-632X

Coppola, Antonietta and Hernandez-Hernandez, Laura and Balestrini, Simona and Krithika, S. and Moran, Nicholas and Hale, Blake and Cordivari, Carla and Sisodiya, Sanjay M. (2020) Cortical myoclonus and epilepsy in a family with a new SLC20A2 mutation. Journal of Neurology, 267 (8). pp. 2221-2227. ISSN 1432-1459

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

Coppola, Antonietta and Morrogh, Deborah and Farrell, Fiona and Balestrini, Simona and Hernandez-Hernandez, Laura and Krithika, S. and Sander, Josemir W. and Waters, Jonathan J. and Sisodiya, Sanjay M. (2018) Ring Chromosome 17 Not Involving the Miller-Dieker Region: A Case with Drug-Resistant Epilepsy. Molecular Syndromology, 9 (1). pp. 38-44. ISSN 1661-8777

This list was generated on Fri May 14 02:17:29 2021 BST.