Enterovirus A71 Infection and Neurologic Disease, Madrid, Spain, 2016 von Taravilla, Carmen Niño, Pérez-Sebastián, Isabel, Salido, Alberto García, Serrano, Claudia Varela, Extremera, Verónica Cantarín, Rodríguez, Anna Duat, Marín, Laura López, Sanz, Mercedes Alonso, Traba, Olga María Suárez, González, Ana Serrano

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Tocilizumab in pediatric refractory status epilepticus and acute epilepsy: Experience in two patients von Cantarín-Extremera, Verónica, Jiménez-Legido, María, Duat-Rodríguez, Anna, García-Fernández, Marta, Ortiz-Cabrera, Nelmar Valentina, Ruiz-Falcó-Rojas, María Luz, González-Gutiérrez-Solana, Luis

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Neuropsychiatric comorbidities and cognition in epilepsy with eyelid myoclonia: A retrospective pediatric case series von Ballarà Petitbò, Maria, González Alguacil, Elena, Gutiérrez Delicado, Eva, Ortiz Cabrera, Nelmar Valentina, Duat Rodríguez, Anna, García Peñas, Juan José, Soto Insuga, Victor

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Early Diagnosis of CAPOS Syndrome Before Acute-Onset Ataxia—Review of the Literature and a New Family von Duat Rodriguez, Anna, MD, PhD, Prochazkova, Michaela, MD, Santos Santos, Saturnino, MD, Rubio Cabezas, Oscar, MD, PhD, Cantarin Extremera, Veronica, MD, Gonzalez-Gutierrez-Solana, Luis, MD

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Neurofibromatosis Type 1 Associated With Moyamoya Syndrome in Children von Duat-Rodríguez, Anna, MD, Carceller Lechón, Fernando, MD, López Pino, Miguel Ángel, MD, Rodríguez Fernández, Cristina, MD, González-Gutiérrez-Solana, Luis, MD

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Hemicerebellitis: Report of three paediatric cases and review of the literature von Carceller Lechón, Fernando, Duat Rodríguez, Anna, Sirvent Cerdá, Sara I, Khabra, Komel, de Prada, Inmaculada, García-Peñas, Juan Jose, Madero López, Luis

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High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype Correla... von Rojnueangnit, Kitiwan, Xie, Jing, Gomes, Alicia, Sharp, Angela, Callens, Tom, Chen, Yunjia, Liu, Ying, Cochran, Meagan, Abbott, Mary-Alice, Atkin, Joan, Babovic-Vuksanovic, Dusica, Barnett, Christopher P., Crenshaw, Melissa, Bartholomew, Dennis W., Basel, Lina, Bellus, Gary, Ben-Shachar, Shay, Bialer, Martin G., Bick, David, Blumberg, Bruce, Cortes, Fanny, David, Karen L., Destree, Anne, Duat-Rodriguez, Anna, Earl, Dawn, Escobar, Luis, Eswara, Marthanda, Ezquieta, Begona, Frayling, Ian M., Frydman, Moshe, Gardner, Kathy, Gripp, Karen W., Hernández-Chico, Concepcion, Heyrman, Kurt, Ibrahim, Jennifer, Janssens, Sandra, Keena, Beth A, Llano-Rivas, Isabel, Leppig, Kathy, McDonald, Marie, Misra, Vinod K., Mulbury, Jennifer, Narayanan, Vinodh, Orenstein, Naama, Galvin-Parton, Patricia, Pedro, Helio, Pivnick, Eniko K., Powell, Cynthia M., Randolph, Linda, Raskin, Salmo, Rosell, Jordi, Rubin, Karol, Seashore, Margretta, Schaaf, Christian P., Scheuerle, Angela, Schultz, Meredith, Schorry, Elizabeth, Schnur, Rhonda, Siqveland, Elizabeth, Tkachuk, Amanda, Tonsgard, James, Upadhyaya, Meena, Verma, Ishwar C., Wallace, Stephanie, Williams, Charles, Zackai, Elaine, Zonana, Jonathan, Lazaro, Conxi, Claes, Kathleen, Korf, Bruce, Martin, Yolanda, Legius, Eric, Messiaen, Ludwine

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Anatomo-Electro-Clinical Phenotypes in Children With Epilepsy and DYNC1H1 Mutations von Gutiérrez-Delicado, Eva, García-Fernández, Marta, Ortiz Cabrera, Nelmar Valentina, Soto Insuga, Víctor, Justel Rodríguez, María, Duat-Rodríguez, Anna, Caicoya, Anne G., Álvarez-Linera Prado, Juan, Solís Muñiz, Inés, Pérez-Jiménez, María Ángeles

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Clinical Case of Anti- N -methyl- d -aspartate Receptor Encephalitis in an 8-Month-Old Patient With Hyperkinetic Movement Disorder von Cantarín-Extremera, Verónica, MD, Duat-Rodríguez, Anna, MD, González-Gutiérrez-Solana, Luis, MD, López-Marín, Laura, MD, Armangue, Thaís, MD

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Congenital cutaneous neurofibromas in neurofibromatosis type 1: Clinicopathological features in early infancy von García‐Martínez, Francisco Javier, Azorín, Daniel, Duat‐Rodríguez, Anna, Hernández‐Martín, Ángela

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Immune-Mediated Mechanisms in the Pathogenesis of Hopkins Syndrome von Cantarín-Extremera, Verónica, MD, González-Gutiérrez-Solana, Luis, MD, Ramírez-Orellana, Manuel, MD, PhD, López-Marín, Laura, MD, Duat-Rodríguez, Anna, MD, Ruíz-Falcó-Rojas, Maria Luz, MD

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Facial Capillary Malformation and Dyke-Davidoff-Masson Syndrome von Bagazgoitia, Lorea, MD, García-Peñas, Juan José, MD, Duat-Rodríguez, Anna, MD, Hernández-Martín, Ángela, MD, Torrelo, Antonio, MD

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Utility of the transcranial doppler in the evaluation and follow-up of children with Sturge-Weber Syndrome von Jiménez-Legido, María, Martínez-de-Azagra-Garde, Amelia, Bernardino-Cuesta, Beatriz, Solís-Muñiz, Inés, Soto-Insuga, Víctor, Cantarín-Extremera, Verónica, García-Salido, Alberto, Duat-Rodríguez, Anna, García-Peñas, Juan José, Ruíz-Falcó-Rojas, María Luz

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Cutaneous and Systemic Findings in Mosaic Neurofibromatosis Type 1 von Vázquez‐Osorio, Igor, Duat‐Rodríguez, Anna, García‐Martínez, Francisco Javier, Torrelo, Antonio, Noguera‐Morel, Lucero, Hernández‐Martín, Angela

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Secondary Intracranial Hypertension in Pediatric Patients With Leukemia von Fernández-García, Miguel Ángel, Cantarín-Extremera, Verónica, Andión-Catalán, Maitane, Duat-Rodríguez, Anna, Jiménez-Echevarría, Saioa, Bermejo-Arnedo, Ignacio, Hortigüela-Saeta, Montesclaros, Rekarte-García, Saray, Babín-López, Lara, Ruano Domínguez, David

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Induced atypical absence seizures during treatment with perampanel von Duat Rodríguez, Anna, Cantarín Extremera, Verónica, García Fernández, Marta, García Peñas, Juan José, Ruiz-Falcó Rojas, María Luz

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Dystonia and Contractures are Potential Early Signs of CACNA1E-Related Epileptic Encephalopathy von Ortiz Cabrera, Nelmar V., Duat Rodríguez, Anna, Fernández Garoz, Bárbara, Bernardino Cuesta, Beatriz, Jiménez Legido, María, Cantarín Extremera, Verónica, García Peñas, Juan J.

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The LINCE Project: A Pathway for Diagnosing NCL2 Disease von Rodrigues, Daniel, de Castro, Maria José, Crujeiras, Pablo, Duat-Rodriguez, Anna, Marco, Ana Victoria, Del Toro, Mireia, Couce, María L, Colón, Cristóbal

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Characteristics and evolution of patients with Alice in Wonderland syndrome von Losada-Del Pozo, Rebeca, Cantarín-Extremera, Verónica, García-Peñas, Juan J, Duat-Rodríguez, Anna, López-Marín, Laura, Gutiérrez-Solana, Luis G, Ruiz-Falcó, M Luz

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ATP1A3-related disorders in the differential diagnosis of acute brainstem and cerebellar dysfunction von Duat-Rodríguez, Anna, Prochazkova, Michaela, Sebastian, Isabel Perez, Extremera, Veronica Cantarin, Legido, Maria Jimenez, Palero, Serafin Rodriguez, Ortiz Cabrera, Nelmar Valentina

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