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Thomas N Ferraro

Showing results (81-90 of 86) with videos related to

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Genes|September 28, 2021
Genetic Variation in <i>PADI6-PADI4</i> on 1p36.13 Is Associated with Common Forms of Human Generalized EpilepsyRussell J Buono, Jonathan P Bradfield, Zhi Wei, et al.
Clinical Drug Investigation|August 1, 2025
Memantine for the Treatment of Primary Negative Symptoms in Schizophrenia: A Meta-analysis of Randomized Controlled TrialsHoulin Hong, Jack Donlon, Martin Schaefer, et al.
Plos One|November 1, 2023
Postmortem toxicology findings from the Camden Opioid Research InitiativeDara M Kusic, Jessica Heil, Stefan Zajic, et al.
Brain Sciences|January 8, 2025
Galantamine-Memantine Combination in the Treatment of Parkinson's Disease DementiaEmma D Frost, Swanny X Shi, Vishnu V Byroju, et al.
Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Science (New York, N.Y.)|June 23, 2018
Analysis of shared heritability in common disorders of the brain, Verneri Anttila, Brendan Bulik-Sullivan, et al.
Pageof 9

Showing results (81-90 of 86) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 86 results.
Genes|September 28, 2021
Genetic Variation in <i>PADI6-PADI4</i> on 1p36.13 Is Associated with Common Forms of Human Generalized EpilepsyRussell J Buono, Jonathan P Bradfield, Zhi Wei, et al.
Clinical Drug Investigation|August 1, 2025
Memantine for the Treatment of Primary Negative Symptoms in Schizophrenia: A Meta-analysis of Randomized Controlled TrialsHoulin Hong, Jack Donlon, Martin Schaefer, et al.
Plos One|November 1, 2023
Postmortem toxicology findings from the Camden Opioid Research InitiativeDara M Kusic, Jessica Heil, Stefan Zajic, et al.
Brain Sciences|January 8, 2025
Galantamine-Memantine Combination in the Treatment of Parkinson's Disease DementiaEmma D Frost, Swanny X Shi, Vishnu V Byroju, et al.
Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Science (New York, N.Y.)|June 23, 2018
Analysis of shared heritability in common disorders of the brain, Verneri Anttila, Brendan Bulik-Sullivan, et al.
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