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Pediatrics
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May 14, 2014
Common genetic variants and risk of brain injury after preterm birth
James P Boardman, Andrew Walley, Gareth Ball, et al.
Nature Reviews. Drug Discovery
|
May 18, 2021
Clinical trial strategies for rare neurodevelopmental disorders: challenges and opportunities
Michelle L Krishnan, Elizabeth Berry-Kravis, Jamie K Capal, et al.
Nature Communications
|
September 7, 2017
Integrative genomics of microglia implicates DLG4 (PSD95) in the white matter development of preterm infants
Michelle L Krishnan, Juliette Van Steenwinckel, Anne-Laure Schang, et al.
Nature Medicine
|
July 11, 2025
The UBE3A-ATS antisense oligonucleotide rugonersen in children with Angelman syndrome: a phase 1 trial
Jörg F Hipp, Carlos A Bacino, Lynne M Bird, et al.
Journal of Neurodevelopmental Disorders
|
July 26, 2023
Enabling endpoint development for interventional clinical trials in individuals with Angelman syndrome: a prospective, longitudinal, observational clinical study (FREESIAS)
Jorrit Tjeertes, Carlos A Bacino, Terry Jo Bichell, et al.
Brain : a Journal of Neurology
|
October 31, 2019
Decreased microglial Wnt/β-catenin signalling drives microglial pro-inflammatory activation in the developing brain
Juliette Van Steenwinckel, Anne-Laure Schang, Michelle L Krishnan, et al.
Plos One
|
March 18, 2025
Correction: A natural history study to track brain and spinal cord changes in individuals with Friedreich's ataxia: TRACK-FA study protocol
Nellie Georgiou-Karistianis, Louise A Corben, Kathrin Reetz, et al.
Plos One
|
November 21, 2022
A natural history study to track brain and spinal cord changes in individuals with Friedreich's ataxia: TRACK-FA study protocol
Nellie Georgiou-Karistianis, Louise A Corben, Kathrin Reetz, et al.
Nature Communications
|
January 24, 2015
Systems genetics identifies Sestrin 3 as a regulator of a proconvulsant gene network in human epileptic hippocampus
Michael R Johnson, Jacques Behmoaras, Leonardo Bottolo, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
Pediatrics
|
May 14, 2014
Common genetic variants and risk of brain injury after preterm birth
James P Boardman, Andrew Walley, Gareth Ball, et al.
Nature Reviews. Drug Discovery
|
May 18, 2021
Clinical trial strategies for rare neurodevelopmental disorders: challenges and opportunities
Michelle L Krishnan, Elizabeth Berry-Kravis, Jamie K Capal, et al.
Nature Communications
|
September 7, 2017
Integrative genomics of microglia implicates DLG4 (PSD95) in the white matter development of preterm infants
Michelle L Krishnan, Juliette Van Steenwinckel, Anne-Laure Schang, et al.
Nature Medicine
|
July 11, 2025
The UBE3A-ATS antisense oligonucleotide rugonersen in children with Angelman syndrome: a phase 1 trial
Jörg F Hipp, Carlos A Bacino, Lynne M Bird, et al.
Journal of Neurodevelopmental Disorders
|
July 26, 2023
Enabling endpoint development for interventional clinical trials in individuals with Angelman syndrome: a prospective, longitudinal, observational clinical study (FREESIAS)
Jorrit Tjeertes, Carlos A Bacino, Terry Jo Bichell, et al.
Brain : a Journal of Neurology
|
October 31, 2019
Decreased microglial Wnt/β-catenin signalling drives microglial pro-inflammatory activation in the developing brain
Juliette Van Steenwinckel, Anne-Laure Schang, Michelle L Krishnan, et al.
Plos One
|
March 18, 2025
Correction: A natural history study to track brain and spinal cord changes in individuals with Friedreich's ataxia: TRACK-FA study protocol
Nellie Georgiou-Karistianis, Louise A Corben, Kathrin Reetz, et al.
Plos One
|
November 21, 2022
A natural history study to track brain and spinal cord changes in individuals with Friedreich's ataxia: TRACK-FA study protocol
Nellie Georgiou-Karistianis, Louise A Corben, Kathrin Reetz, et al.
Nature Communications
|
January 24, 2015
Systems genetics identifies Sestrin 3 as a regulator of a proconvulsant gene network in human epileptic hippocampus
Michael R Johnson, Jacques Behmoaras, Leonardo Bottolo, et al.
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of 2