Search Results - Villeneuve, Nathalie

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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Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes by Endele, Sabine (Author) , Rosenberger, Georg (Author) , Geider, Kirsten (Author) , Popp, Bernt (Author) , Tamer, Ceyhun (Author) , Stefanova, Irina (Author) , Milh, Mathieu (Author) , Kortüm, Fanny (Author) , Fritsch, Angela (Author) , Pientka, Friederike K. (Author) , Hellenbroich, Yorck (Author) , Kalscheuer, Vera M. (Author) , Kohlhase, Jürgen (Author) , Moog, Ute (Author) , Rappold, Gudrun (Author) , Rauch, Anita (Author) , Ropers, Hans-Hilger (Author) , von Spiczak, Sarah (Author) , Tönnies, Holger (Author) , Villeneuve, Nathalie (Author) , Villard, Laurent (Author) , Zabel, Bernhard (Author) , Zenker, Martin (Author) , Laube, Bodo (Author) , Reis, André (Author) , Wieczorek, Dagmar (Author) , Van Maldergem, Lionel (Author) , Kutsche, Kerstin (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes

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