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Showing results (41-50 of 138) with videos related to

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Cephalalgia : an International Journal of Headache|August 22, 2012
A replication study of a GWAS finding in migraine does not identify association in a Spanish case-control sampleCèlia Sintas, Oriel Carreño, Jèssica Fernández-Morales, et al.
Molecular Genetics and Metabolism|November 13, 2012
Characterisation of two deletions involving NPC1 and flanking genes in Niemann-Pick type C disease patientsLaura Rodríguez-Pascau, Claudio Toma, Judit Macías-Vidal, et al.
Journal of the Neurological Sciences|July 6, 2014
Clinical and genetic analysis in alternating hemiplegia of childhood: ten new patients from Southern EuropeMarta Vila-Pueyo, Roser Pons, Miquel Raspall-Chaure, et al.
Addiction Biology|October 8, 2014
Frustrated expected reward induces differential transcriptional changes in the mouse brainElena Martín-García, Noelia Fernández-Castillo, Aurelijus Burokas, et al.
Genes|January 21, 2022
Exploring the Contribution to ADHD of Genes Involved in Mendelian Disorders Presenting with Hyperactivity and/or InattentionNoèlia Fernàndez-Castillo, Judit Cabana-Domínguez, Djenifer B Kappel, et al.
Journal of Inherited Metabolic Disease|September 22, 2010
Progressive ataxia and myoclonic epilepsy in a patient with a homozygous mutation in the FOLR1 geneBelén Pérez-Dueñas, Claudio Toma, Aida Ormazábal, et al.
Molecular Genetics and Metabolism|August 19, 2007
A homozygous tyrosine hydroxylase gene promoter mutation in a patient with dopa-responsive encephalopathy: clinical, biochemical and genetic analysisMarta Ribasés, Mercedes Serrano, Emilio Fernández-Alvarez, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 14, 2011
SNP variants within the vanilloid TRPV1 and TRPV3 receptor genes are associated with migraine in the Spanish populationOriel Carreño, Roser Corominas, Jessica Fernández-Morales, et al.
Biorxiv : the Preprint Server for Biology|October 28, 2024
<i>rbfox1</i> loss in zebrafish drives HPI axis hyperactivation via <i>bdnf/trkb2</i> pathway and allostatic overload during later lifeAdele Leggieri, Judit García-González, Saeedeh Hosseinian, et al.
Translational Psychiatry|November 19, 2025
rbfox1 LoF mutants show disrupted bdnf/trkb2 and crhb/nr3c2 expression and increased cortisol levels during development coupled with signs of allostatic overload in adulthoodAdele Leggieri, Judit García-González, Saeedeh Hosseinian, et al.
Pageof 14

Showing results (41-50 of 138) with videos related to

Sort By:
Pageof 14
Cephalalgia : an International Journal of Headache|August 22, 2012
A replication study of a GWAS finding in migraine does not identify association in a Spanish case-control sampleCèlia Sintas, Oriel Carreño, Jèssica Fernández-Morales, et al.
Molecular Genetics and Metabolism|November 13, 2012
Characterisation of two deletions involving NPC1 and flanking genes in Niemann-Pick type C disease patientsLaura Rodríguez-Pascau, Claudio Toma, Judit Macías-Vidal, et al.
Journal of the Neurological Sciences|July 6, 2014
Clinical and genetic analysis in alternating hemiplegia of childhood: ten new patients from Southern EuropeMarta Vila-Pueyo, Roser Pons, Miquel Raspall-Chaure, et al.
Addiction Biology|October 8, 2014
Frustrated expected reward induces differential transcriptional changes in the mouse brainElena Martín-García, Noelia Fernández-Castillo, Aurelijus Burokas, et al.
Genes|January 21, 2022
Exploring the Contribution to ADHD of Genes Involved in Mendelian Disorders Presenting with Hyperactivity and/or InattentionNoèlia Fernàndez-Castillo, Judit Cabana-Domínguez, Djenifer B Kappel, et al.
Journal of Inherited Metabolic Disease|September 22, 2010
Progressive ataxia and myoclonic epilepsy in a patient with a homozygous mutation in the FOLR1 geneBelén Pérez-Dueñas, Claudio Toma, Aida Ormazábal, et al.
Molecular Genetics and Metabolism|August 19, 2007
A homozygous tyrosine hydroxylase gene promoter mutation in a patient with dopa-responsive encephalopathy: clinical, biochemical and genetic analysisMarta Ribasés, Mercedes Serrano, Emilio Fernández-Alvarez, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 14, 2011
SNP variants within the vanilloid TRPV1 and TRPV3 receptor genes are associated with migraine in the Spanish populationOriel Carreño, Roser Corominas, Jessica Fernández-Morales, et al.
Biorxiv : the Preprint Server for Biology|October 28, 2024
<i>rbfox1</i> loss in zebrafish drives HPI axis hyperactivation via <i>bdnf/trkb2</i> pathway and allostatic overload during later lifeAdele Leggieri, Judit García-González, Saeedeh Hosseinian, et al.
Translational Psychiatry|November 19, 2025
rbfox1 LoF mutants show disrupted bdnf/trkb2 and crhb/nr3c2 expression and increased cortisol levels during development coupled with signs of allostatic overload in adulthoodAdele Leggieri, Judit García-González, Saeedeh Hosseinian, et al.
Pageof 14