Search Results - Lesca, Gaétan

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  1. 1
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    De novo variants in RAB11B cause various degrees of lobal developmental delay and intellectual disability in children by Ahmad, Natalie (Author) , Fazeli, Walid (Author) , Schließke, Sophia (Author) , Lesca, Gaetan (Author) , Gokce-Samar, Zeynep (Author) , Mekbib, Kedous Y. (Author) , Jin, Sheng Chih (Author) , Burton, Jennifer (Author) , Hoganson, George (Author) , Petersen, Andrea (Author) , Gracie, Sara (Author) , Granger, Leslie (Author) , Bartels, Enrika (Author) , Oppermann, Henry (Author) , Kundishora, Adam (Author) , Till, Marianne (Author) , Milleret-Pignot, Clara (Author) , Dangerfield, Shane (Author) , Viskochil, David (Author) , Anderson, Katherine J. (Author) , Palculict, Timothy Blake (Author) , Schnur, Rhonda E. (Author) , Wentzensen, Ingrid M. (Author) , Tiller, George E. (Author) , Kahle, Kristopher T. (Author) , Kunz, Wolfram S. (Author) , Burkart, Sebastian (Author) , Simons, Matias (Author) , Sticht, Heinrich (Author) , Abou Jamra, Rami (Author) , Neuser, Sonja (Author) ,


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  2. 2
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    The gain of function SCN1A disorder spectrum: novel epilepsy phenotypes and therapeutic implications by Brunklaus, Andreas (Author) , Brünger, Tobias (Author) , Feng, Tony (Author) , Fons, Carmen (Author) , Lehikoinen, Anni (Author) , Panagiotakaki, Eleni (Author) , Vintan, Mihaela-Adela (Author) , Symonds, Joseph (Author) , Andrew, James (Author) , Arzimanoglou, Alexis (Author) , Delima, Sarah (Author) , Gallois, Julie (Author) , Hanrahan, Donncha (Author) , Lesca, Gaetan (Author) , MacLeod, Stewart (Author) , Marjanovic, Dragan (Author) , McTague, Amy (Author) , Nuñez-Enamorado, Noemi (Author) , Perez-Palma, Eduardo (Author) , Scott Perry, M (Author) , Pysden, Karen (Author) , Russ-Hall, Sophie J (Author) , Scheffer, Ingrid E (Author) , Sully, Krystal (Author) , Syrbe, Steffen (Author) , Vaher, Ulvi (Author) , Velayutham, Murugan (Author) , Vogt, Julie (Author) , Weiss, Shelly (Author) , Wirrell, Elaine (Author) , Zuberi, Sameer M (Author) , Lal, Dennis (Author) , Møller, Rikke S (Author) , Mantegazza, Massimo (Author) , Cestèle, Sandrine (Author) ,


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  3. 3
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    Refining genotypes and phenotypes in KCNA2-related neurological disorders by Driedger, Jan Henje (Author) , Schröter, Julian (Author) , Jüngling, Jerome (Author) , Biskup, Saskia (Author) , Klotz, Kerstin A. (Author) , Bast, Thomas (Author) , Dietel, Tobias (Author) , Korenke, Christoph (Author) , Christoph, Sophie (Author) , Brennenstuhl, Heiko (Author) , Rubboli, Guido (Author) , Møller, Rikke S. (Author) , Lesca, Gaetan (Author) , Chaix, Yves (Author) , Kölker, Stefan (Author) , Hoffmann, Georg F. (Author) , Lemke, Johannes (Author) , Syrbe, Steffen (Author) ,


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  4. 4
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    ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria by Vetro, Annalisa (Author) , Nielsen, Hang N (Author) , Holm, Rikke (Author) , Hevner, Robert F (Author) , Parrini, Elena (Author) , Powis, Zoe (Author) , Møller, Rikke S (Author) , Bellan, Cristina (Author) , Simonati, Alessandro (Author) , Lesca, Gaétan (Author) , Helbig, Katherine L (Author) , Palmer, Elizabeth E (Author) , Mei, Davide (Author) , Ballardini, Elisa (Author) , Van Haeringen, Arie (Author) , Syrbe, Steffen (Author) , Leuzzi, Vincenzo (Author) , Cioni, Giovanni (Author) , Curry, Cynthia J (Author) , Costain, Gregory (Author) , Santucci, Margherita (Author) , Chong, Karen (Author) , Mancini, Grazia M S (Author) , Clayton-Smith, Jill (Author) , Bigoni, Stefania (Author) , Scheffer, Ingrid E (Author) , Dobyns, William B (Author) , Vilsen, Bente (Author) , Guerrini, Renzo (Author) ,


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  5. 5
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    KCNT1-related epilepsies and epileptic encephalopathies: phenotypic and mutational spectrum by Bonardi, Claudia M. (Author) , Heyne, Henrike O (Author) , Fiannacca, Martina (Author) , Fitzgerald, Mark P (Author) , Gardella, Elena (Author) , Gunning, Boudewijn (Author) , Olofsson, Kern (Author) , Lesca, Gaétan (Author) , Verbeek, Nienke (Author) , Stamberger, Hannah (Author) , Striano, Pasquale (Author) , Zara, Federico (Author) , Mancardi, Maria M (Author) , Nava, Caroline (Author) , Syrbe, Steffen (Author) , Buono, Salvatore (Author) , Baulac, Stephanie (Author) , Coppola, Antonietta (Author) , Weckhuysen, Sarah (Author) , Schoonjans, An-Sofie (Author) , Ceulemans, Berten (Author) , Sarret, Catherine (Author) , Baumgartner, Tobias (Author) , Muhle, Hiltrud (Author) , Portes, Vincent des (Author) , Toulouse, Joseph (Author) , Nougues, Marie-Christine (Author) , Rossi, Massimiliano (Author) , Demarquay, Geneviève (Author) , Ville, Dorothée (Author) , Hirsch, Edouard (Author) , Maurey, Hélène (Author) , Willems, Marjolaine (Author) , de Bellescize, Julitta (Author) , Altuzarra, Cecilia Desmettre (Author) , Villeneuve, Nathalie (Author) , Bartolomei, Fabrice (Author) , Picard, Fabienne (Author) , Hornemann, Frauke (Author) , Koolen, David A (Author) , Kroes, Hester Y (Author) , Reale, Chiara (Author) , Fenger, Christina D (Author) , Tan, Wen-Hann (Author) , Dibbens, Leanne (Author) , Bearden, David R (Author) , Møller, Rikke S (Author) , Rubboli, Guido (Author) ,


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  6. 6
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    New insights into the clinical and molecular spectrum of the novel CYFIP2-related neurodevelopmental disorder and impairment of the WRC-mediated actin dynamics by Begemann, Anaïs (Author) , Sticht, Heinrich (Author) , Begtrup, Amber (Author) , Vitobello, Antonio (Author) , Faivre, Laurence (Author) , Banka, Siddharth (Author) , Alhaddad, Bader (Author) , Asadollahi, Reza (Author) , Becker, Jessica (Author) , Bierhals, Tatjana (Author) , Brown, Kathleen E. (Author) , Bruel, Ange-Line (Author) , Brunet, Theresa (Author) , Carneiro, Maryline (Author) , Cremer, Kirsten (Author) , Day, Robert (Author) , Denommé-Pichon, Anne-Sophie (Author) , Dyment, Dave A. (Author) , Engels, Hartmut (Author) , Fisher, Rachel (Author) , Goh, Elaine S. (Author) , Hajianpour, M. J. (Author) , Haertel, Lucia Ribeiro Machado (Author) , Hauer, Nadine (Author) , Hempel, Maja (Author) , Herget, Theresia (Author) , Johannsen, Jessika (Author) , Kraus, Cornelia (Author) , Le Guyader, Gwenaël (Author) , Lesca, Gaetan (Author) , Mau-Them, Frédéric Tran (Author) , McDermott, John Henry (Author) , McWalter, Kirsty (Author) , Meyer, Pierre (Author) , Õunap, Katrin (Author) , Popp, Bernt (Author) , Reimand, Tiia (Author) , Riedhammer, Korbinian M. (Author) , Russo, Martina (Author) , Sadleir, Lynette G. (Author) , Saenz, Margarita (Author) , Schiff, Manuel (Author) , Schuler, Elisabeth (Author) , Syrbe, Steffen (Author) , Van der Ven, Amelie Theresa (Author) , Verloes, Alain (Author) , Willems, Marjolaine (Author) , Zweier, Christiane (Author) , Steindl, Katharina (Author) , Zweier, Markus (Author) , Rauch, Anita (Author) ,


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  7. 7
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    Phenotypic and imaging spectrum associated wth WDR45 by Adang, Laura A. (Author) , Pizzino, Amy (Author) , Malhotra, Alka (Author) , Dubbs, Holly (Author) , Williams, Catherine (Author) , Sherbini, Omar (Author) , Anttonen, Anna-Kaisa (Author) , Lesca, Gaetan (Author) , Linnankivi, Tarja (Author) , Laurencin, Chloé (Author) , Milh, Matthieu (Author) , Perrine, Charles (Author) , Schaaf, Christian P. (Author) , Poulat, Anne-Lise (Author) , Ville, Dorothee (Author) , Hagelstrom, Tanner (Author) , Perry, Denise L. (Author) , Taft, Ryan J. (Author) , Goldstein, Amy (Author) , Vossough, Arastoo (Author) , Helbig, Ingo (Author) , Vanderver, Adeline (Author) ,


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  8. 8
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    Treatment responsiveness in KCNT1-related epilepsy by Fitzgerald, Mark P. (Author) , Fiannacca, Martina (Author) , Smith, Douglas M. (Author) , Gertler, Tracy S. (Author) , Gunning, Boudewijn (Author) , Syrbe, Steffen (Author) , Verbeek, Nienke (Author) , Stamberger, Hannah (Author) , Weckhuysen, Sarah (Author) , Ceulemans, Berten (Author) , Schoonjans, An-Sofie (Author) , Rossi, Massimiliano (Author) , Demarquay, Geneviève (Author) , Lesca, Gaetan (Author) , Olofsson, Kern (Author) , Koolen, D. A. (Author) , Hornemann, Frauke (Author) , Baulac, Stephanie (Author) , Rubboli, Guido (Author) , Minks, Kelly Q. (Author) , Lee, Bohoon (Author) , Helbig, Ingo (Author) , Dlugos, Dennis (Author) , Møller, Rikke S. (Author) , Bearden, David (Author) ,


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  9. 9
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    Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy by XiangWei, Wenshu (Author) , Kannan, Varun (Author) , Xu, Yuchen (Author) , Kosobucki, Gabrielle J. (Author) , Schulien, Anthony J. (Author) , Kusumoto, Hirofumi (Author) , Moufawad El Achkar, Christelle (Author) , Bhattacharya, Subhrajit (Author) , Lesca, Gaetan (Author) , Nguyen, Sylvie (Author) , Helbig, Katherine L. (Author) , Cuisset, Jean-Marie (Author) , Fenger, Christina Dühring (Author) , Marjanovic, Dragan (Author) , Schuler, Elisabeth (Author) , Wu, Ye (Author) , Bao, Xinhua (Author) , Zhang, Yuehua (Author) , Dirkx, Nina (Author) , Schoonjans, An-Sofie (Author) , Syrbe, Steffen (Author) , Myers, Scott J. (Author) , Poduri, Annapurna (Author) , Aizenman, Elias (Author) , Traynelis, Stephen F. (Author) , Lemke, Johannes (Author) , Yuan, Hongjie (Author) , Jiang, Yuwu (Author) ,


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