A novel human Cdh1 mutation impairs anaphase promoting complex/cyclosome activity resulting in microcephaly, psychomotor retardation, and epilepsy von Rodríguez, Cristina, Sánchez‐Morán, Irene, Álvarez, Sara, Tirado, Pilar, Fernández‐Mayoralas, Daniel M., Calleja‐Pérez, Beatriz, Almeida, Ángeles, Fernández‐Jaén, Alberto

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Tatton‐Brown–Rahman syndrome: Novel pathogenic variants and new neuroimaging findings von Jiménez de la Peña, Mar, Rincón‐Pérez, Irene, López‐Martín, Sara, Albert, Jacobo, Martín Fernández‐Mayoralas, Daniel, Fernández‐Perrone, Ana Laura, Jiménez de Domingo, Ana, Tirado, Pilar, Calleja‐Pérez, Beatriz, Porta, Javier, Álvarez, Sara, Fernández‐Jaén, Alberto

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ANO3 and early-onset dyskinetic encephalopathy von Jiménez de Domingo, Ana, Lopez-Martín, Sara, Albert, Jacobo, Jiménez de la Peña, Mar, Tirado, Pilar, Fernández-Mayoralas, Daniel Martín, Fernández-Perrone, Ana Laura, Calleja-Pérez, Beatriz, Martínez-García, Mónica, Álvarez, Sara, Fernández-Jaén, Alberto

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Cerebral palsy, epilepsy, and severe intellectual disability in a patient with 3q29 microduplication syndrome von Fernández-Jaén, Alberto, Castellanos, María del Carmen, Fernández-Perrone, Ana Laura, Fernández-Mayoralas, Daniel Martín, de la Vega, Alberto González, Calleja-Pérez, Beatriz, Fernández, Ester Corbacho, Albert, Jacobo, Hombre, María Carmen Sánchez

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Cortical Thickness in Fetal Alcohol Syndrome and Attention Deficit Disorder von Fernández-Jaén, Alberto, MD, Fernández-Mayoralas, Daniel Martín, MD, PhD, Quiñones Tapia, Diana, MD, Calleja-Pérez, Beatriz, MD, García-Segura, Juan Manuel, MD, Arribas, Sonia López, MD, Muñoz Jareño, Nuria, MD, PhD

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Microduplication 10q24.31 in a Spanish girl with scoliosis and myopathy: The critical role of LBX von Fernández-Jaén, Alberto, Suela, Javier, Fernández-Mayoralas, Daniel Martín, Fernández-Perrone, Ana Laura, Wotton, Karl R., Dietrich, Susanne, Castellanos, Maria del Carmen, Cigudosa, Juan C., Calleja-Pérez, Beatriz, López-Martín, Sara

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Atomoxetine for Attention Deficit Hyperactivity Disorder in Mental Retardation von FERNANDEZ-JAEN, Alberto, FERNANDEZ-MAYORALAS, Daniel Martin, CALLEJA PEREZ, Beatriz, MUNOZ JARENO, Nuria, CAMPOS DIAZ, Maria Del Rosario

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Fetal Alcohol Syndrome, Tourette Syndrome, and Hyperactivity in Nine Adopted Children von Fernández-Mayoralas, Daniel Martín, MD, PhD, Fernández-Jaén, Alberto, MD, Muñoz-Jareño, Nuria, MD, Calleja Pérez, Beatriz, MD, Arroyo-González, Rafael, MD, PhD

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Gomez–Lopez-Hernandez Syndrome: Two New Cases and Review of the Literature von Fernández-Jaén, Alberto, MD, Fernández-Mayoralas, Daniel Martín, MD, Calleja-Pérez, Beatriz, MD, Muñoz-Jareño, Nuria, MD, Moreno, Noelia, MD

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Biallelic SYNE2 Missense Mutations Leading to Nesprin-2 Giant Hypo-Expression Are Associated with Intellectual Disability and Autism von Young, Natalie, Asif, Maria, Jackson, Matthew, Fernández-Mayoralas, Daniel Martín, de la Peña, Mar Jimenez, Calleja-Pérez, Beatriz, Álvarez, Sara, Hunter-Featherstone, Eve, Noegel, Angelika A, Höhne, Wolfgang, Nürnberg, Peter, Obara, Boguslaw, Hussain, Muhammad Sajid, Karakesisoglou, Iakowos, Fernández-Jaén, Alberto

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Mutations in BRAT1 Cause Autosomal Recessive Progressive Encephalopathy: Report of a Spanish Patient von Fernández-Jaén, Alberto, Dr, Álvarez, Sara, So, Eui Young, Ouchi, Toru, Jiménez de la Peña, Mar, Duat, Anna, Fernández-Mayoralas, Daniel Martín, Fernández-Perrone, Ana Laura, Albert, Jacobo, Calleja-Pérez, Beatriz

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A Novel Loss-of-Function SEMA3E Mutation in a Patient with Severe Intellectual Disability and Cognitive Regression von Paganoni, Alyssa J J, Amoruso, Federica, Porta Pelayo, Javier, Calleja-Pérez, Beatriz, Vezzoli, Valeria, Duminuco, Paolo, Caramello, Alessia, Oleari, Roberto, Fernández-Jaén, Alberto, Cariboni, Anna

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An open-label, prospective study of levetiracetam in children and adolescentes with Tourette syndrome von Fernández-Jaén, Alberto, Fernández-Mayoralas, Daniel Martín, Muñoz-Jareño, Nuria, Calleja-Pérez, Beatriz

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Autism and attention deficit hyperactivity disorder: pharmacological intervention von Fernández-Jaén, Alberto, Martín Fernández-Mayoralas, Daniel, Fernández-Perrone, Ana Laura, Calleja-Pérez, Beatriz, Muñoz-Jareño, Nuria, López-Arribas, Sonia

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Meralgia Paresthetica in the Pediatric Population: A Propos of 2 Cases von Fernández-Mayoralas, Daniel Martín, Fernández-Jaén, Alberto, Jareño, Nuria Muñoz, Pérez, Beatriz Calleja, Fernández, Pedro Moreno, Sola, Antonio Guerrero

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Genomic endophenotypes of attention deficit hyperactivity disorder von Fernández-Jaén, Alberto, Fernández-Mayoralas, Daniel Martín, Calleja-Pérez, Beatriz, Muñoz-Jareño, Nuria, López-Arribas, Sonia

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Clinical and cognitive response to extended-release methylphenidate (Medikinet®) in attention deficit/hyperactivity disorder: Efficacy evaluation von Fernández-Jaén, Alberto, Fernández-Mayoralas, Daniel Martín, Pardos, Alexandra, Calleja-Pérez, Beatriz, Muñoz Jareño, Nuria

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Cortical thinning of temporal pole and orbitofrontal cortex in medication-naïve children and adolescents with ADHD von Fernández-Jaén, Alberto, López-Martín, Sara, Albert, Jacobo, Fernández-Mayoralas, Daniel Martín, Fernández-Perrone, Ana Laura, Tapia, Diana Quiñones, Calleja-Pérez, Beatriz

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Neurodesarrollo y fenocopias del trastorno por déficit de atención/hiperactividad: diagnóstico diferencial von Fernández Jaén, Alberto, Martín Fernández-Mayoralas, Daniel, Fernández Perrone, Ana Laura, Jiménez de Domingo, Ana, Albert Bitaubé, Jacobo, López Martín, Sara, Calleja Pérez, Beatriz, Tirado Requero, María Pilar, López Arribas, Sonia

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Cortical thickness differences in the prefrontal cortex in children and adolescents with ADHD in relation to dopamine transporter (DAT1) genotype von Fernández-Jaén, Alberto, López-Martín, Sara, Albert, Jacobo, Fernández-Mayoralas, Daniel Martín, Fernández-Perrone, Ana Laura, de La Peña, Mar Jiménez, Calleja-Pérez, Beatriz, Rodríguez, Manuel Recio, López-Arribas, Sonia, Muñoz-Jareño, Nuria

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