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Annals of Clinical and Translational Neurology
|
September 5, 2015
PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy
Michael S Hildebrand, Rick Tankard, Elena V Gazina, et al.
Circulation
|
August 21, 2023
Improved Cardiac Function in Postischemic Rats Using an Optimized Cardiac Reprogramming Cocktail Delivered in a Single Novel Adeno-Associated Virus
Huanyu Zhou, Jin Yang, Chetan Srinath, et al.
Brain : a Journal of Neurology
|
April 22, 2026
Collapse of feed-forward inhibition underpins hyperexcitability in GABAA gain-of-function epilepsy
Chaseley E McKenzie, Khaing Phyu Aung, Altair Brito Dos Santos, et al.
Nature Communications
|
March 4, 2025
AAV9-mediated MYBPC3 gene therapy with optimized expression cassette enhances cardiac function and survival in MYBPC3 cardiomyopathy models
Amara Greer-Short, Anna Greenwood, Elena C Leon, et al.
Annals of Neurology
|
April 6, 2017
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K<sup>+</sup> channel properties
Karen L Oliver, Silvana Franceschetti, Carol J Milligan, et al.
Nature Communications
|
August 7, 2024
Male autism spectrum disorder is linked to brain aromatase disruption by prenatal BPA in multimodal investigations and 10HDA ameliorates the related mouse phenotype
Christos Symeonides, Kristina Vacy, Sarah Thomson, et al.
Brain : a Journal of Neurology
|
November 17, 2023
Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40
Angela T Morgan, Thomas S Scerri, Adam P Vogel, et al.
Annals of Neurology
|
June 5, 2025
HCN2-Associated Neurodevelopmental Disorders: Data from Patients and Xenopus Cell Models
Clara Houdayer, A Marie Phillips, Marie Chabbert, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 2, 2024
Mono and biallelic variants in <i>HCN2</i> cause severe neurodevelopmental disorders
Clara Houdayer, A Marie Phillips, Marie Chabbert, et al.
The Journal of Clinical Investigation
|
November 25, 2025
Functional consequence of pathogenic GABRA3 variants determines whether X-linked inheritance is dominant or recessive
Katrine M Johannesen, Khaing Phyu Aung, Vivian Wy Liao, et al.
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of 14
Search research articles
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Showing results (121-130 of 131) with videos related to
Sort By:
Page
of 14
Annals of Clinical and Translational Neurology
|
September 5, 2015
PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy
Michael S Hildebrand, Rick Tankard, Elena V Gazina, et al.
Circulation
|
August 21, 2023
Improved Cardiac Function in Postischemic Rats Using an Optimized Cardiac Reprogramming Cocktail Delivered in a Single Novel Adeno-Associated Virus
Huanyu Zhou, Jin Yang, Chetan Srinath, et al.
Brain : a Journal of Neurology
|
April 22, 2026
Collapse of feed-forward inhibition underpins hyperexcitability in GABAA gain-of-function epilepsy
Chaseley E McKenzie, Khaing Phyu Aung, Altair Brito Dos Santos, et al.
Nature Communications
|
March 4, 2025
AAV9-mediated MYBPC3 gene therapy with optimized expression cassette enhances cardiac function and survival in MYBPC3 cardiomyopathy models
Amara Greer-Short, Anna Greenwood, Elena C Leon, et al.
Annals of Neurology
|
April 6, 2017
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K<sup>+</sup> channel properties
Karen L Oliver, Silvana Franceschetti, Carol J Milligan, et al.
Nature Communications
|
August 7, 2024
Male autism spectrum disorder is linked to brain aromatase disruption by prenatal BPA in multimodal investigations and 10HDA ameliorates the related mouse phenotype
Christos Symeonides, Kristina Vacy, Sarah Thomson, et al.
Brain : a Journal of Neurology
|
November 17, 2023
Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40
Angela T Morgan, Thomas S Scerri, Adam P Vogel, et al.
Annals of Neurology
|
June 5, 2025
HCN2-Associated Neurodevelopmental Disorders: Data from Patients and Xenopus Cell Models
Clara Houdayer, A Marie Phillips, Marie Chabbert, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 2, 2024
Mono and biallelic variants in <i>HCN2</i> cause severe neurodevelopmental disorders
Clara Houdayer, A Marie Phillips, Marie Chabbert, et al.
The Journal of Clinical Investigation
|
November 25, 2025
Functional consequence of pathogenic GABRA3 variants determines whether X-linked inheritance is dominant or recessive
Katrine M Johannesen, Khaing Phyu Aung, Vivian Wy Liao, et al.
Page
of 14