Molecular diagnosis of patients with epilepsy and developmental delay using a customized panel of epilepsy genes

por Ortega-Moreno, Laura, Giráldez, Beatriz G., Soto-Insuga, Victor, Losada-Del Pozo, Rebeca, Rodrigo-Moreno, María, Alarcón-Morcillo, Cristina, Sánchez-Martín, Gema, Díaz-Gómez, Esther, Guerrero-López, Rosa, Serratosa, José M.
Publicado 2017

Proposed Recommendations for the Management of Depression in Adults with Epilepsy: An Expert Consensus

por Villanueva, Vicente, Artal, Jesús, Cabeza-Alvarez, Clara-Isabel, Campos, Dulce, Castillo, Ascensión, Flórez, Gerardo, Franco-Martin, Manuel, García-Portilla, María Paz, Giráldez, Beatriz G., Gotor, Francisco, Gutiérrez-Rojas, Luis, Albanell, Albert Molins, Paniagua, Gonzalo, Pintor, Luis, Poza, Juan José, Rubio-Granero, Teresa, Toledo, Manuel, Tortosa-Conesa, Diego, Rodríguez-Uranga, Juan, Bobes, Julio
Publicado 2023

Pitfalls in genetic testing: the story of missed SCN1A mutations

por Djémié, Tania, Weckhuysen, Sarah, von Spiczak, Sarah, Carvill, Gemma L., Jaehn, Johanna, Anttonen, Anna‐Kaisa, Brilstra, Eva, Caglayan, Hande S., de Kovel, Carolien G., Depienne, Christel, Gaily, Eija, Gennaro, Elena, Giraldez, Beatriz G., Gormley, Padhraig, Guerrero‐López, Rosa, Guerrini, Renzo, Hämäläinen, Eija, Hartmann, Corinna, Hernandez‐Hernandez, Laura, Hjalgrim, Helle, Koeleman, Bobby P. C., Leguern, Eric, Lehesjoki, Anna‐Elina, Lemke, Johannes R., Leu, Costin, Marini, Carla, McMahon, Jacinta M., Mei, Davide, Møller, Rikke S., Muhle, Hiltrud, Myers, Candace T., Nava, Caroline, Serratosa, Jose M., Sisodiya, Sanjay M., Stephani, Ulrich, Striano, Pasquale, van Kempen, Marjan J. A., Verbeek, Nienke E., Usluer, Sunay, Zara, Federico, Palotie, Aarno, Mefford, Heather C., Scheffer, Ingrid E., De Jonghe, Peter, Helbig, Ingo, Suls, Arvid
Publicado 2016