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Jacobo Albert

Showing results (51-60 of 57) with videos related to

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Molecular Syndromology|April 14, 2022
Bi-Allelic c.1746G>T; p.Leu582= Variants in <i>TUBGCP4</i> in a Boy with Autism: Clinical Data and Literature ReviewDaniel Martín Fernández-Mayoralas, Jacobo Albert, Sara López-Martín, et al.
Actas Espanolas De Psiquiatria|August 29, 2019
Attention-deficit/hyperactivity disorder and lifestyle habits in children and adolescentsJuan Luis Párraga, Beatriz Calleja Pérez, Sara López-Martín, et al.
Medicina|February 19, 2019
[Attention deficit/hyperactivity disorder. Study habits]Beatriz Calleja-Pérez, Juan L Párraga, Jacobo Albert, et al.
Neurocase|March 7, 2022
Mutations in the COL18A1 gen associated with knobloch syndrome and structural brain anomalies: a novel case report and literature review of neuroimaging findingsI Irene Díez García-Prieto, Sara Lopez-Martín, Jacobo Albert, et al.
European Journal of Medical Genetics|October 12, 2020
ANO3 and early-onset dyskinetic encephalopathyAna Jiménez de Domingo, Sara Lopez-Martín, Jacobo Albert, et al.
American Journal of Medical Genetics. Part A|October 5, 2023
Tatton-Brown-Rahman syndrome: Novel pathogenic variants and new neuroimaging findingsMar Jiménez de la Peña, Irene Rincón-Pérez, Sara López-Martín, et al.
Applied Neuropsychology. Child|September 2, 2021
A mild clinical and neuropsychological phenotype of Renpenning syndrome: A new case report with a maternally inherited <i>PQBP1</i> missense mutationSara Lopez-Martín, Jacobo Albert, Mᵃ Del Mar Peña Vila-Belda, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Molecular Syndromology|April 14, 2022
Bi-Allelic c.1746G>T; p.Leu582= Variants in <i>TUBGCP4</i> in a Boy with Autism: Clinical Data and Literature ReviewDaniel Martín Fernández-Mayoralas, Jacobo Albert, Sara López-Martín, et al.
Actas Espanolas De Psiquiatria|August 29, 2019
Attention-deficit/hyperactivity disorder and lifestyle habits in children and adolescentsJuan Luis Párraga, Beatriz Calleja Pérez, Sara López-Martín, et al.
Medicina|February 19, 2019
[Attention deficit/hyperactivity disorder. Study habits]Beatriz Calleja-Pérez, Juan L Párraga, Jacobo Albert, et al.
Neurocase|March 7, 2022
Mutations in the COL18A1 gen associated with knobloch syndrome and structural brain anomalies: a novel case report and literature review of neuroimaging findingsI Irene Díez García-Prieto, Sara Lopez-Martín, Jacobo Albert, et al.
European Journal of Medical Genetics|October 12, 2020
ANO3 and early-onset dyskinetic encephalopathyAna Jiménez de Domingo, Sara Lopez-Martín, Jacobo Albert, et al.
American Journal of Medical Genetics. Part A|October 5, 2023
Tatton-Brown-Rahman syndrome: Novel pathogenic variants and new neuroimaging findingsMar Jiménez de la Peña, Irene Rincón-Pérez, Sara López-Martín, et al.
Applied Neuropsychology. Child|September 2, 2021
A mild clinical and neuropsychological phenotype of Renpenning syndrome: A new case report with a maternally inherited <i>PQBP1</i> missense mutationSara Lopez-Martín, Jacobo Albert, Mᵃ Del Mar Peña Vila-Belda, et al.
Pageof 6