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Jacobo Albert

Showing results (41-50 of 57) with videos related to

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Medicina|February 23, 2023
[The impact of ADHD on reading]Alberto J Sánchez-Carmona, Jacobo Albert, Sara López-Martín, et al.
Medicina|February 16, 2022
[Neuropsychological deficit, symptom intensity and functional impairment in attention deficit hyperactivity disorder]Jacobo Albert, Alberto J Sánchez-Carmona, Sara López-Martín, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 8, 2014
Cortical thickness at the time of the initial attack in two patients with paediatric relapsing-remitting multiple sclerosisAlberto Fernández-Jaén, Daniel Martín Fernández-Mayoralas, Ana Laura Fernández-Perrone, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 8, 2016
Mutations in BRAT1 cause autosomal recessive progressive encephalopathy: Report of a Spanish patientAlberto Fernández-Jaén, Sara Álvarez, Eui Young So, et al.
Journal of Attention Disorders|May 11, 2016
Cingulate Cortical Thickness and Dopamine Transporter ( DAT1) Genotype in Children and Adolescents With ADHDAlberto Fernández-Jaén, Jacobo Albert, Daniel Martín Fernández-Mayoralas, et al.
Medicina|February 28, 2025
[Computerized cognitive training as a treatment for ADHD: evidence summary and future directions]Jacobo Albert, Sara López-Martín, Alberto J Sánchez-Carmona, et al.
American Journal of Medical Genetics. Part A|May 20, 2014
Cerebral palsy, epilepsy, and severe intellectual disability in a patient with 3q29 microduplication syndromeAlberto Fernández-Jaén, María del Carmen Castellanos, Ana Laura Fernández-Perrone, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 21, 2021
Abnormal frontal gyrification pattern and uncinate development in patients with KBG syndrome caused by ANKRD11 aberrationsMar Jiménez de la Peña, Daniel Martín Fernández-Mayoralas, Sara López-Martín, et al.
Molecular Genetics & Genomic Medicine|January 26, 2025
Early Severe Cortical Involvement and Novel FUCA1 Mutations in a Pediatric Fucosidosis CaseMar Jiménez de la Peña, Sara López-Martín, Daniel Martín Fernández-Mayoralas, et al.
Psychiatry Research|July 25, 2015
Cortical thickness differences in the prefrontal cortex in children and adolescents with ADHD in relation to dopamine transporter (DAT1) genotypeAlberto Fernández-Jaén, Sara López-Martín, Jacobo Albert, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
Medicina|February 23, 2023
[The impact of ADHD on reading]Alberto J Sánchez-Carmona, Jacobo Albert, Sara López-Martín, et al.
Medicina|February 16, 2022
[Neuropsychological deficit, symptom intensity and functional impairment in attention deficit hyperactivity disorder]Jacobo Albert, Alberto J Sánchez-Carmona, Sara López-Martín, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 8, 2014
Cortical thickness at the time of the initial attack in two patients with paediatric relapsing-remitting multiple sclerosisAlberto Fernández-Jaén, Daniel Martín Fernández-Mayoralas, Ana Laura Fernández-Perrone, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 8, 2016
Mutations in BRAT1 cause autosomal recessive progressive encephalopathy: Report of a Spanish patientAlberto Fernández-Jaén, Sara Álvarez, Eui Young So, et al.
Journal of Attention Disorders|May 11, 2016
Cingulate Cortical Thickness and Dopamine Transporter ( DAT1) Genotype in Children and Adolescents With ADHDAlberto Fernández-Jaén, Jacobo Albert, Daniel Martín Fernández-Mayoralas, et al.
Medicina|February 28, 2025
[Computerized cognitive training as a treatment for ADHD: evidence summary and future directions]Jacobo Albert, Sara López-Martín, Alberto J Sánchez-Carmona, et al.
American Journal of Medical Genetics. Part A|May 20, 2014
Cerebral palsy, epilepsy, and severe intellectual disability in a patient with 3q29 microduplication syndromeAlberto Fernández-Jaén, María del Carmen Castellanos, Ana Laura Fernández-Perrone, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 21, 2021
Abnormal frontal gyrification pattern and uncinate development in patients with KBG syndrome caused by ANKRD11 aberrationsMar Jiménez de la Peña, Daniel Martín Fernández-Mayoralas, Sara López-Martín, et al.
Molecular Genetics & Genomic Medicine|January 26, 2025
Early Severe Cortical Involvement and Novel FUCA1 Mutations in a Pediatric Fucosidosis CaseMar Jiménez de la Peña, Sara López-Martín, Daniel Martín Fernández-Mayoralas, et al.
Psychiatry Research|July 25, 2015
Cortical thickness differences in the prefrontal cortex in children and adolescents with ADHD in relation to dopamine transporter (DAT1) genotypeAlberto Fernández-Jaén, Sara López-Martín, Jacobo Albert, et al.
Pageof 6