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Bru Cormand

Showing results (61-70 of 138) with videos related to

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Cephalalgia : an International Journal of Headache|February 9, 2023
Genome-wide DNA methylation analysis in an antimigraine-treated preclinical model of cortical spreading depolarizationMarta Vila-Pueyo, Ester Cuenca-León, Ana C Queirós, et al.
Scientific Reports|June 2, 2017
Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic AtaxiaCèlia Sintas, Oriel Carreño, Noèlia Fernàndez-Castillo, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|March 24, 2011
Candidate pathway association study in cocaine dependence: the control of neurotransmitter releaseNoèlia Fernàndez-Castillo, Bru Cormand, Carlos Roncero, et al.
Journal of Psychiatric Research|October 5, 2010
Association study of six candidate genes asymmetrically expressed in the two cerebral hemispheres suggests the involvement of BAIAP2 in autismClaudio Toma, Amaia Hervás, Noemí Balmaña, et al.
Scientific Reports|January 14, 2018
A De Novo FOXP1 Truncating Mutation in a Patient Originally Diagnosed as C SyndromeRoser Urreizti, Sarah Damanti, Carla Esteve, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 16, 2015
Dopamine receptor DRD4 gene and stressful life events in persistent attention deficit hyperactivity disorderCristina Sánchez-Mora, Vanesa Richarte, Iris Garcia-Martínez, et al.
Translational Psychiatry|February 19, 2024
Pleiotropic contribution of rbfox1 to psychiatric and neurodevelopmental phenotypes in two zebrafish modelsEster Antón-Galindo, Maja R Adel, Judit García-González, et al.
Journal of the Neurological Sciences|February 24, 2009
Late-onset episodic ataxia type 2 associated with a novel loss-of-function mutation in the CACNA1A geneEster Cuenca-León, Isabel Banchs, Selma A Serra, et al.
Journal of Psychiatric Research|September 12, 2020
Exploring allele specific methylation in drug dependence susceptibilityLaura Pineda-Cirera, Judit Cabana-Domínguez, Lara Grau-López, et al.
Psychiatry Research|October 15, 2013
Lack of association between the LPR and VNTR polymorphisms of the serotonin transporter gene and cocaine dependence in a Spanish sampleAlba Tristán-Noguero, Noèlia Fernàndez-Castillo, Carlos Roncero, et al.
Pageof 14

Showing results (61-70 of 138) with videos related to

Sort By:
Pageof 14
Cephalalgia : an International Journal of Headache|February 9, 2023
Genome-wide DNA methylation analysis in an antimigraine-treated preclinical model of cortical spreading depolarizationMarta Vila-Pueyo, Ester Cuenca-León, Ana C Queirós, et al.
Scientific Reports|June 2, 2017
Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic AtaxiaCèlia Sintas, Oriel Carreño, Noèlia Fernàndez-Castillo, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|March 24, 2011
Candidate pathway association study in cocaine dependence: the control of neurotransmitter releaseNoèlia Fernàndez-Castillo, Bru Cormand, Carlos Roncero, et al.
Journal of Psychiatric Research|October 5, 2010
Association study of six candidate genes asymmetrically expressed in the two cerebral hemispheres suggests the involvement of BAIAP2 in autismClaudio Toma, Amaia Hervás, Noemí Balmaña, et al.
Scientific Reports|January 14, 2018
A De Novo FOXP1 Truncating Mutation in a Patient Originally Diagnosed as C SyndromeRoser Urreizti, Sarah Damanti, Carla Esteve, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 16, 2015
Dopamine receptor DRD4 gene and stressful life events in persistent attention deficit hyperactivity disorderCristina Sánchez-Mora, Vanesa Richarte, Iris Garcia-Martínez, et al.
Translational Psychiatry|February 19, 2024
Pleiotropic contribution of rbfox1 to psychiatric and neurodevelopmental phenotypes in two zebrafish modelsEster Antón-Galindo, Maja R Adel, Judit García-González, et al.
Journal of the Neurological Sciences|February 24, 2009
Late-onset episodic ataxia type 2 associated with a novel loss-of-function mutation in the CACNA1A geneEster Cuenca-León, Isabel Banchs, Selma A Serra, et al.
Journal of Psychiatric Research|September 12, 2020
Exploring allele specific methylation in drug dependence susceptibilityLaura Pineda-Cirera, Judit Cabana-Domínguez, Lara Grau-López, et al.
Psychiatry Research|October 15, 2013
Lack of association between the LPR and VNTR polymorphisms of the serotonin transporter gene and cocaine dependence in a Spanish sampleAlba Tristán-Noguero, Noèlia Fernàndez-Castillo, Carlos Roncero, et al.
Pageof 14