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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
January 30, 2009
Genetically determined interaction between the dopamine transporter and the D2 receptor on prefronto-striatal activity and volume in humans
Alessandro Bertolino, Leonardo Fazio, Annabella Di Giorgio, et al.
American Journal of Medical Genetics. Part A
|
June 24, 2020
TUBB3 E410K syndrome: Case report and review of the clinical spectrum of TUBB3 mutations
Maria L Dentici, Vittorio Maglione, Emanuele Agolini, et al.
Social Cognitive and Affective Neuroscience
|
July 31, 2012
DAT by perceived MC interaction on human prefrontal activity and connectivity during emotion processing
Paolo Taurisano, Giuseppe Blasi, Raffaella Romano, et al.
Schizophrenia Bulletin
|
October 7, 2011
DRD2 genotype-based variation of default mode network activity and of its relationship with striatal DAT binding
Fabio Sambataro, Leonardo Fazio, Paolo Taurisano, et al.
Frontiers in Genetics
|
July 15, 2022
Genetics of Inherited Retinal Diseases in Understudied Ethnic Groups in Italian Hospitals
Paolo Enrico Maltese, Leonardo Colombo, Salvatore Martella, et al.
Brain Sciences
|
November 14, 2020
7q11.23 Microduplication Syndrome: Clinical and Neurobehavioral Profiling
Maria Lisa Dentici, Paola Bergonzini, Francesco Scibelli, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
November 27, 2009
Functional variation of the dopamine D2 receptor gene is associated with emotional control as well as brain activity and connectivity during emotion processing in humans
Giuseppe Blasi, Luciana Lo Bianco, Paolo Taurisano, et al.
Biological Psychiatry
|
April 1, 2008
Epistasis between dopamine regulating genes identifies a nonlinear response of the human hippocampus during memory tasks
Alessandro Bertolino, Annabella Di Giorgio, Giuseppe Blasi, et al.
American Journal of Medical Genetics. Part A
|
December 31, 2021
Congenital heart defects in molecularly confirmed KBG syndrome patients
Maria Cristina Digilio, Giulio Calcagni, Maria Gnazzo, et al.
Genes
|
April 27, 2024
Spectrum of <i>ERCC6</i>-Related Cockayne Syndrome (Type B): From Mild to Severe Forms
Jacopo Sartorelli, Lorena Travaglini, Marina Macchiaiolo, et al.
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of 6
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Showing results (31-40 of 57) with videos related to
Sort By:
Page
of 6
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
January 30, 2009
Genetically determined interaction between the dopamine transporter and the D2 receptor on prefronto-striatal activity and volume in humans
Alessandro Bertolino, Leonardo Fazio, Annabella Di Giorgio, et al.
American Journal of Medical Genetics. Part A
|
June 24, 2020
TUBB3 E410K syndrome: Case report and review of the clinical spectrum of TUBB3 mutations
Maria L Dentici, Vittorio Maglione, Emanuele Agolini, et al.
Social Cognitive and Affective Neuroscience
|
July 31, 2012
DAT by perceived MC interaction on human prefrontal activity and connectivity during emotion processing
Paolo Taurisano, Giuseppe Blasi, Raffaella Romano, et al.
Schizophrenia Bulletin
|
October 7, 2011
DRD2 genotype-based variation of default mode network activity and of its relationship with striatal DAT binding
Fabio Sambataro, Leonardo Fazio, Paolo Taurisano, et al.
Frontiers in Genetics
|
July 15, 2022
Genetics of Inherited Retinal Diseases in Understudied Ethnic Groups in Italian Hospitals
Paolo Enrico Maltese, Leonardo Colombo, Salvatore Martella, et al.
Brain Sciences
|
November 14, 2020
7q11.23 Microduplication Syndrome: Clinical and Neurobehavioral Profiling
Maria Lisa Dentici, Paola Bergonzini, Francesco Scibelli, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
November 27, 2009
Functional variation of the dopamine D2 receptor gene is associated with emotional control as well as brain activity and connectivity during emotion processing in humans
Giuseppe Blasi, Luciana Lo Bianco, Paolo Taurisano, et al.
Biological Psychiatry
|
April 1, 2008
Epistasis between dopamine regulating genes identifies a nonlinear response of the human hippocampus during memory tasks
Alessandro Bertolino, Annabella Di Giorgio, Giuseppe Blasi, et al.
American Journal of Medical Genetics. Part A
|
December 31, 2021
Congenital heart defects in molecularly confirmed KBG syndrome patients
Maria Cristina Digilio, Giulio Calcagni, Maria Gnazzo, et al.
Genes
|
April 27, 2024
Spectrum of <i>ERCC6</i>-Related Cockayne Syndrome (Type B): From Mild to Severe Forms
Jacopo Sartorelli, Lorena Travaglini, Marina Macchiaiolo, et al.
Page
of 6