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Endokrynologia Polska
|
January 27, 2023
The effect of vitamin D status on non-alcoholic fatty liver disease: a population-based observational study
Kursat Dal, Metin Uzman, Naim Ata, et al.
The Journal of Clinical Investigation
|
March 23, 2023
Intrathecal AAV9/AP4M1 gene therapy for hereditary spastic paraplegia 50 shows safety and efficacy in preclinical studies
Xin Chen, Thomas Dong, Yuhui Hu, et al.
Nature Communications
|
May 19, 2021
16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitro
Maria Sundberg, Hannah Pinson, Richard S Smith, et al.
Neurology
|
September 21, 2021
Systematic Analysis of Brain MRI Findings in Adaptor Protein Complex 4-Associated Hereditary Spastic Paraplegia
Darius Ebrahimi-Fakhari, Julian E Alecu, Marvin Ziegler, et al.
Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging
|
July 16, 2019
Resting-State fMRI Networks in Children with Tuberous Sclerosis Complex
Banu Ahtam, Mathieu Dehaes, Danielle D Sliva, et al.
Pediatric Neurology
|
June 9, 2016
Leveraging a Sturge-Weber Gene Discovery: An Agenda for Future Research
Anne M Comi, Mustafa Sahin, Adrienne Hammill, et al.
Epilepsy & Behavior : E&B
|
November 7, 2018
Electrographic spikes are common in wildtype mice
Hannah Purtell, Sameer C Dhamne, Sarika Gurnani, et al.
Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society
|
July 2, 2019
Lesion-Constrained Electrical Source Imaging: A Novel Approach in Epilepsy Surgery for Tuberous Sclerosis Complex
Jurriaan M Peters, Damon E Hyde, Catherine J Chu, et al.
Nature Reviews. Drug Discovery
|
April 3, 2019
Discovering translational biomarkers in neurodevelopmental disorders
Mustafa Sahin, Stephanie R Jones, John A Sweeney, et al.
Epilepsia
|
March 24, 2025
Epilepsy surgery in Sturge-Weber syndrome with unilateral or bilateral asymmetric brain involvement: Boston Children's Hospital experience
Michelle Y Chiu, Isabelle Iannotti, Matheus D Soldatelli, et al.
Page
of 60
Search research articles
Search
Showing results (421-430 of 597) with videos related to
Sort By:
Page
of 60
Endokrynologia Polska
|
January 27, 2023
The effect of vitamin D status on non-alcoholic fatty liver disease: a population-based observational study
Kursat Dal, Metin Uzman, Naim Ata, et al.
The Journal of Clinical Investigation
|
March 23, 2023
Intrathecal AAV9/AP4M1 gene therapy for hereditary spastic paraplegia 50 shows safety and efficacy in preclinical studies
Xin Chen, Thomas Dong, Yuhui Hu, et al.
Nature Communications
|
May 19, 2021
16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitro
Maria Sundberg, Hannah Pinson, Richard S Smith, et al.
Neurology
|
September 21, 2021
Systematic Analysis of Brain MRI Findings in Adaptor Protein Complex 4-Associated Hereditary Spastic Paraplegia
Darius Ebrahimi-Fakhari, Julian E Alecu, Marvin Ziegler, et al.
Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging
|
July 16, 2019
Resting-State fMRI Networks in Children with Tuberous Sclerosis Complex
Banu Ahtam, Mathieu Dehaes, Danielle D Sliva, et al.
Pediatric Neurology
|
June 9, 2016
Leveraging a Sturge-Weber Gene Discovery: An Agenda for Future Research
Anne M Comi, Mustafa Sahin, Adrienne Hammill, et al.
Epilepsy & Behavior : E&B
|
November 7, 2018
Electrographic spikes are common in wildtype mice
Hannah Purtell, Sameer C Dhamne, Sarika Gurnani, et al.
Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society
|
July 2, 2019
Lesion-Constrained Electrical Source Imaging: A Novel Approach in Epilepsy Surgery for Tuberous Sclerosis Complex
Jurriaan M Peters, Damon E Hyde, Catherine J Chu, et al.
Nature Reviews. Drug Discovery
|
April 3, 2019
Discovering translational biomarkers in neurodevelopmental disorders
Mustafa Sahin, Stephanie R Jones, John A Sweeney, et al.
Epilepsia
|
March 24, 2025
Epilepsy surgery in Sturge-Weber syndrome with unilateral or bilateral asymmetric brain involvement: Boston Children's Hospital experience
Michelle Y Chiu, Isabelle Iannotti, Matheus D Soldatelli, et al.
Page
of 60