Salzburg Criteria, A Useful Tool in Non-Convulsive Status Epilepticus Diagnosis: A Retrospective Study von Domínguez, Adriana Gómez, Mateo Montero, Raidili C., Díaz Cid, Alba, Mazarro, Antonio J. P., Bailly-Bailliere, Ignacio R., Landete, Isabel M. S., Palomeque, Guillermo M.

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New spinocerebellar ataxia subtype caused by SAMD9L mutation triggering mitochondrial dysregulation (SCA49) von Corral-Juan, Marc, Casquero, Pilar, Giraldo-Restrepo, Natalia, Laurie, Steve, Martinez-Piñeiro, Alicia, Mateo-Montero, Raidili Cristina, Ispierto, Lourdes, Vilas, Dolores, Tolosa, Eduardo, Volpini, Victor, Alvarez-Ramo, Ramiro, Sánchez, Ivelisse, Matilla-Dueñas, Antoni

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Clinical and genetical study of a familial form of REM sleep behavior disorder von Mateo-Montero, Raidili Cristina, Pedrera-Mazarro, Antonio, Martín-Palomeque, Guillermo, del Mar Moreno-Galera, María, Valera-Dávila, Carlos, Gómez-Ansede, Alicia, Braun, Jorge, Jiménez-Escrig, Adriano

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WE-187. Utility and clinical outcome using standard IONM techniques in patients with high-risk neuromuscular scoliosis von Mateo Montero, Raidili, Jones, Eric, Cho, Charles, Lee, Leslie, Le, Scheherazade, Nguyen, Viet, Lopez, Jaime

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S26. Description and prognostic value of EEG in patients in coma after recovered cardiorespiratory arrest von Mateo-Montero, Raidili, Martin-Palomeque, Guillermo, Valera, Carlos, Gómez-Ansede, Alicia, Pedrera-Mazarro, Antonio, González-Rodriguez, Liliana, Regidor, Ignacio

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S50. Facioscapulohumeral muscular distrophy: Presentation of a case with clinical-genetic discordance von Cabañes-Martinez, Lidia, Mateo-Montero, Raidili, López-Viñas, Laura, Gómez-Ansede, Alicia, Regidor, Ignacio, Jiménez-Escrig, Adriano

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P88-T Clinical and neurophysiologic characterization of the diabetic truncal mononeuropathy von Rodríguez, Liliana González, Montero, Raidili Mateo, Martinez, Lidia Cabañes, Domínguez, Adriana Gómez, Villadóniga, Marta, de Blas, Gema, Bally-Bailliere, Ignacio Regidor

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New spinocerebellar ataxia subtype caused by SAMD9L mutation triggering mitochondrial dysregulation (SCA49) von Corral Juan, Marc, Casquero, Pilar, Giraldo Restrepo, Natalia, Laurie, Steve, Martinez Piñeiro, Alicia, Mateo Montero, Raidili Cristina, Ispierto, Lourdes, Vilas, Dolores, Tolosa, Eduardo, Volpini, Victor, Alvarez Ramo, Ramiro, Sánchez, Ivelisse, Matilla Dueñas, Antoni

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New spinocerebellar ataxia subtype caused by SAMD9L mutation triggering mitochondrial dysregulation (SCA49) von Corral Juan, Marc, Casquero, Pilar, Giraldo-Restrepo, Natalia, Laurie, Steven, 1973, Martinez-Piñeiro, Alicia, Mateo-Montero, Raidili Cristina, Ispierto, Lourdes, Vilas, Dolores, Tolosa, Eduard, Volpini, Victor, Alvarez-Ramo, Ramiro, Sánchez, Ivelisse, Matilla Dueñas, Antoni

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New spinocerebellar ataxia subtype caused by SAMD9L mutation triggering mitochondrial dysregulation (SCA49) von Corral-Juan, Marc, Casquero, Pilar, Giraldo-Restrepo, Natalia, Laurie, Steve, Martínez-Piñeiro, Alicia, Mateo-Montero, Raidili Cristina, Ispierto, Lourdes, Vilas, Dolores, Tolosa, Eduardo, Volpini, Víctor, Álvarez, Ramiro, Sánchez, Ivelisse, Matilla-Dueñas, Antoni, Universitat Autònoma de Barcelona

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New spinocerebellar ataxia subtype caused by SAMD9L mutation triggering mitochondrial dysregulation (SCA49) von Corral-Juan, Marc, Casquero, Pilar, Giraldo-Restrepo, Natalia, Laurie, Steve, Martínez-Piñeiro, Alicia, Mateo-Montero, Raidili Cristina, Ispierto, Lourdes, Vilas, Dolores, Tolosa, Eduardo, Volpini, Víctor, Álvarez, Ramiro, Sánchez, Ivelisse, Matilla-Dueñas, Antoni, Universitat Autònoma de Barcelona

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