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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
May 6, 2011
Stress-related methylation of the catechol-O-methyltransferase Val 158 allele predicts human prefrontal cognition and activity
Gianluca Ursini, Valentina Bollati, Leonardo Fazio, et al.
Genes
|
October 28, 2023
From Feeding Challenges to Oral-Motor Dyspraxia: A Comprehensive Description of 10 New Cases with CTNNB1 Syndrome
Roberta Onesimo, Elisabetta Sforza, Valentina Trevisan, et al.
American Journal of Medical Genetics. Part A
|
March 4, 2020
KBG syndrome: Common and uncommon clinical features based on 31 new patients
Maria Gnazzo, Francesca R Lepri, Maria Lisa Dentici, et al.
Clinical Genetics
|
June 29, 2025
Further Exploring the TRRAP Genotype-Phenotype Correlations: Report of Three New Patients With A Focus on Skeletal Anomalies
Chiara Minotti, Sara Terreri, Andrea Del Fattore, et al.
Frontiers in Genetics
|
February 20, 2026
Analyzing the genetic profile of autistic children and adolescents with minimal verbal abilities
Silvia Guerrera, Ilaria Venezia, Maria Grazia Logrieco, et al.
Plos One
|
February 25, 2010
Genetically determined measures of striatal D2 signaling predict prefrontal activity during working memory performance
Alessandro Bertolino, Paolo Taurisano, Nicola Marco Pisciotta, et al.
Parkinsonism & Related Disorders
|
July 27, 2024
Movement disorder phenotype in CTNNB1-syndrome: A complex but recognizable phenomenology
Giacomo Garone, Alice Innocenti, Melissa Grasso, et al.
Diagnostics (Basel, Switzerland)
|
March 27, 2024
Congenital Heart Defects in Patients with Molecularly Confirmed Sotos Syndrome
Giulio Calcagni, Federica Ferrigno, Alessio Franceschini, et al.
International Journal of Molecular Sciences
|
July 13, 2024
A Case of CDKL5 Deficiency Due to an X Chromosome Pericentric Inversion: Delineation of Structural Rearrangements as an Overlooked Recurrent Pathological Mechanism
Antonietta Lombardo, Lorenzo Sinibaldi, Silvia Genovese, et al.
JAMA Psychiatry
|
July 12, 2013
Converging evidence for the association of functional genetic variation in the serotonin receptor 2a gene with prefrontal function and olanzapine treatment
Giuseppe Blasi, Caterina De Virgilio, Apostolos Papazacharias, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 57) with videos related to
Sort By:
Page
of 6
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
May 6, 2011
Stress-related methylation of the catechol-O-methyltransferase Val 158 allele predicts human prefrontal cognition and activity
Gianluca Ursini, Valentina Bollati, Leonardo Fazio, et al.
Genes
|
October 28, 2023
From Feeding Challenges to Oral-Motor Dyspraxia: A Comprehensive Description of 10 New Cases with CTNNB1 Syndrome
Roberta Onesimo, Elisabetta Sforza, Valentina Trevisan, et al.
American Journal of Medical Genetics. Part A
|
March 4, 2020
KBG syndrome: Common and uncommon clinical features based on 31 new patients
Maria Gnazzo, Francesca R Lepri, Maria Lisa Dentici, et al.
Clinical Genetics
|
June 29, 2025
Further Exploring the TRRAP Genotype-Phenotype Correlations: Report of Three New Patients With A Focus on Skeletal Anomalies
Chiara Minotti, Sara Terreri, Andrea Del Fattore, et al.
Frontiers in Genetics
|
February 20, 2026
Analyzing the genetic profile of autistic children and adolescents with minimal verbal abilities
Silvia Guerrera, Ilaria Venezia, Maria Grazia Logrieco, et al.
Plos One
|
February 25, 2010
Genetically determined measures of striatal D2 signaling predict prefrontal activity during working memory performance
Alessandro Bertolino, Paolo Taurisano, Nicola Marco Pisciotta, et al.
Parkinsonism & Related Disorders
|
July 27, 2024
Movement disorder phenotype in CTNNB1-syndrome: A complex but recognizable phenomenology
Giacomo Garone, Alice Innocenti, Melissa Grasso, et al.
Diagnostics (Basel, Switzerland)
|
March 27, 2024
Congenital Heart Defects in Patients with Molecularly Confirmed Sotos Syndrome
Giulio Calcagni, Federica Ferrigno, Alessio Franceschini, et al.
International Journal of Molecular Sciences
|
July 13, 2024
A Case of CDKL5 Deficiency Due to an X Chromosome Pericentric Inversion: Delineation of Structural Rearrangements as an Overlooked Recurrent Pathological Mechanism
Antonietta Lombardo, Lorenzo Sinibaldi, Silvia Genovese, et al.
JAMA Psychiatry
|
July 12, 2013
Converging evidence for the association of functional genetic variation in the serotonin receptor 2a gene with prefrontal function and olanzapine treatment
Giuseppe Blasi, Caterina De Virgilio, Apostolos Papazacharias, et al.
Page
of 6