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Bru Cormand

Showing results (71-80 of 138) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|March 4, 2010
Tyrosine hydroxylase deficiency in three Greek patients with a common ancestral mutationRoser Pons, Mercedes Serrano, Aida Ormazabal, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|November 28, 2017
RBFOX1, encoding a splicing regulator, is a candidate gene for aggressive behaviorNoèlia Fernàndez-Castillo, Gabriela Gan, Marjolein M J van Donkelaar, et al.
Neuroscience and Biobehavioral Reviews|November 11, 2022
The translational genetics of ADHD and related phenotypes in model organismsJudit Cabana-Domínguez, Ester Antón-Galindo, Noèlia Fernàndez-Castillo, et al.
American Journal of Medical Genetics. Part A|January 16, 2016
Screening of CD96 and ASXL1 in 11 patients with Opitz C or Bohring-Opitz syndromesRoser Urreizti, Neus Roca-Ayats, Judith Trepat, et al.
Archives of Neurology|May 11, 2011
Cerebral folate deficiency syndromes in childhood: clinical, analytical, and etiologic aspectsBelén Pérez-Dueñas, Aida Ormazábal, Claudio Toma, et al.
Journal of Psychiatric Research|November 26, 2013
Genome-wide copy number variation analysis in adult attention-deficit and hyperactivity disorderJosep-Antoni Ramos-Quiroga, Cristina Sánchez-Mora, Miguel Casas, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 19, 2010
A mutation in the first intracellular loop of CACNA1A prevents P/Q channel modulation by SNARE proteins and lowers exocytosisSelma A Serra, Ester Cuenca-León, Artur Llobet, et al.
Translational Psychiatry|May 29, 2024
Disentangling heterogeneity in substance use disorder: Insights from genome-wide polygenic scoresLaura Vilar-Ribó, Judit Cabana-Domínguez, Silvia Alemany, et al.
Mutation Research|May 22, 2009
Absence of cytogenetic effects in children and adults with attention-deficit/hyperactivity disorder treated with methylphenidateImmaculada Ponsa, Josep Antoni Ramos-Quiroga, Marta Ribasés, et al.
Biological Psychiatry|January 9, 2008
Association study of 10 genes encoding neurotrophic factors and their receptors in adult and child attention-deficit/hyperactivity disorderMarta Ribasés, Amaia Hervás, Josep Antoni Ramos-Quiroga, et al.
Pageof 14

Showing results (71-80 of 138) with videos related to

Sort By:
Pageof 14
Movement Disorders : Official Journal of the Movement Disorder Society|March 4, 2010
Tyrosine hydroxylase deficiency in three Greek patients with a common ancestral mutationRoser Pons, Mercedes Serrano, Aida Ormazabal, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|November 28, 2017
RBFOX1, encoding a splicing regulator, is a candidate gene for aggressive behaviorNoèlia Fernàndez-Castillo, Gabriela Gan, Marjolein M J van Donkelaar, et al.
Neuroscience and Biobehavioral Reviews|November 11, 2022
The translational genetics of ADHD and related phenotypes in model organismsJudit Cabana-Domínguez, Ester Antón-Galindo, Noèlia Fernàndez-Castillo, et al.
American Journal of Medical Genetics. Part A|January 16, 2016
Screening of CD96 and ASXL1 in 11 patients with Opitz C or Bohring-Opitz syndromesRoser Urreizti, Neus Roca-Ayats, Judith Trepat, et al.
Archives of Neurology|May 11, 2011
Cerebral folate deficiency syndromes in childhood: clinical, analytical, and etiologic aspectsBelén Pérez-Dueñas, Aida Ormazábal, Claudio Toma, et al.
Journal of Psychiatric Research|November 26, 2013
Genome-wide copy number variation analysis in adult attention-deficit and hyperactivity disorderJosep-Antoni Ramos-Quiroga, Cristina Sánchez-Mora, Miguel Casas, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 19, 2010
A mutation in the first intracellular loop of CACNA1A prevents P/Q channel modulation by SNARE proteins and lowers exocytosisSelma A Serra, Ester Cuenca-León, Artur Llobet, et al.
Translational Psychiatry|May 29, 2024
Disentangling heterogeneity in substance use disorder: Insights from genome-wide polygenic scoresLaura Vilar-Ribó, Judit Cabana-Domínguez, Silvia Alemany, et al.
Mutation Research|May 22, 2009
Absence of cytogenetic effects in children and adults with attention-deficit/hyperactivity disorder treated with methylphenidateImmaculada Ponsa, Josep Antoni Ramos-Quiroga, Marta Ribasés, et al.
Biological Psychiatry|January 9, 2008
Association study of 10 genes encoding neurotrophic factors and their receptors in adult and child attention-deficit/hyperactivity disorderMarta Ribasés, Amaia Hervás, Josep Antoni Ramos-Quiroga, et al.
Pageof 14