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Human Molecular Genetics
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March 7, 2008
A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome
Rodney C Samaco, John D Fryer, Jun Ren, et al.
Research in Developmental Disabilities
|
April 27, 2023
Learning about neurodiversity from parents - Auditory gestalt perception of prelinguistic vocalisations
Dajie Zhang, Sigrun Lang, Bernd Wilken, et al.
Contemporary Clinical Trials
|
February 12, 2022
Design and outcome measures of LAVENDER, a phase 3 study of trofinetide for Rett syndrome
Jeffrey L Neul, Alan K Percy, Timothy A Benke, et al.
Pediatric Neurology
|
October 2, 2017
A Double-Blind, Randomized, Placebo-Controlled Clinical Study of Trofinetide in the Treatment of Rett Syndrome
Daniel G Glaze, Jeffrey L Neul, Alan Percy, et al.
American Journal of Medical Genetics. Part A
|
May 22, 2024
Rett syndrome diagnostic odyssey: Limitations of NextGen sequencing
Megan Abbott, Katie Angione, Emily Forbes, et al.
Nature Neuroscience
|
August 25, 2014
Mutual antagonism between Sox10 and NFIA regulates diversification of glial lineages and glioma subtypes
Stacey M Glasgow, Wenyi Zhu, C Claus Stolt, et al.
Plos One
|
October 12, 2022
Behavioral and brain anatomical analysis of Foxg1 heterozygous mice
Kirsty R Erickson, Rebekah Farmer, Jonathan K Merritt, et al.
Science Translational Medicine
|
December 11, 2012
Overexpression of methyl-CpG binding protein 2 impairs T(H)1 responses
Tianshu Yang, Melissa B Ramocki, Jeffrey L Neul, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
May 30, 2025
Potentiation of group III metabotropic glutamate receptors positively affects neurophysiological features in a mouse model of Rett syndrome
Hong-Wei Dong, Kelly Weiss, Jonathan W Dickerson, et al.
Journal of Neurodevelopmental Disorders
|
July 26, 2024
Characterizing the journey of Rett syndrome among females in the United States: a real-world evidence study using the Rett syndrome natural history study database
Damian May, Kalé Kponee-Shovein, Jeffrey L Neul, et al.
Page
of 13
Search research articles
Search
Showing results (41-50 of 122) with videos related to
Sort By:
Page
of 13
Human Molecular Genetics
|
March 7, 2008
A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome
Rodney C Samaco, John D Fryer, Jun Ren, et al.
Research in Developmental Disabilities
|
April 27, 2023
Learning about neurodiversity from parents - Auditory gestalt perception of prelinguistic vocalisations
Dajie Zhang, Sigrun Lang, Bernd Wilken, et al.
Contemporary Clinical Trials
|
February 12, 2022
Design and outcome measures of LAVENDER, a phase 3 study of trofinetide for Rett syndrome
Jeffrey L Neul, Alan K Percy, Timothy A Benke, et al.
Pediatric Neurology
|
October 2, 2017
A Double-Blind, Randomized, Placebo-Controlled Clinical Study of Trofinetide in the Treatment of Rett Syndrome
Daniel G Glaze, Jeffrey L Neul, Alan Percy, et al.
American Journal of Medical Genetics. Part A
|
May 22, 2024
Rett syndrome diagnostic odyssey: Limitations of NextGen sequencing
Megan Abbott, Katie Angione, Emily Forbes, et al.
Nature Neuroscience
|
August 25, 2014
Mutual antagonism between Sox10 and NFIA regulates diversification of glial lineages and glioma subtypes
Stacey M Glasgow, Wenyi Zhu, C Claus Stolt, et al.
Plos One
|
October 12, 2022
Behavioral and brain anatomical analysis of Foxg1 heterozygous mice
Kirsty R Erickson, Rebekah Farmer, Jonathan K Merritt, et al.
Science Translational Medicine
|
December 11, 2012
Overexpression of methyl-CpG binding protein 2 impairs T(H)1 responses
Tianshu Yang, Melissa B Ramocki, Jeffrey L Neul, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
May 30, 2025
Potentiation of group III metabotropic glutamate receptors positively affects neurophysiological features in a mouse model of Rett syndrome
Hong-Wei Dong, Kelly Weiss, Jonathan W Dickerson, et al.
Journal of Neurodevelopmental Disorders
|
July 26, 2024
Characterizing the journey of Rett syndrome among females in the United States: a real-world evidence study using the Rett syndrome natural history study database
Damian May, Kalé Kponee-Shovein, Jeffrey L Neul, et al.
Page
of 13