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Scientific Reports
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December 9, 2016
From Function to Phenotype: Impaired DNA Binding and Clustering Correlates with Clinical Severity in Males with Missense Mutations in MECP2
Taimoor I Sheikh, Juan Ausió, Hannah Faghfoury, et al.
Pediatric Neurology
|
October 30, 2024
MECP2 Variants in Males: More Common than Previously Appreciated
Amitha Ananth, Cary Fu, Jeffrey L Neul, et al.
Frontiers in Integrative Neuroscience
|
March 13, 2020
Metabolic Signatures Differentiate Rett Syndrome From Unaffected Siblings
Jeffrey L Neul, Steven A Skinner, Fran Annese, et al.
Pediatric Neurology
|
March 29, 2017
Scoliosis in Rett Syndrome: Progression, Comorbidities, and Predictors
John T Killian, Jane B Lane, Hye-Seung Lee, et al.
The Journal of Pediatrics
|
September 24, 2009
Longevity in Rett syndrome: analysis of the North American Database
Russell S Kirby, Jane B Lane, Jerry Childers, 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.
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.
Neurobiology of Disease
|
May 16, 2009
Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations
Christopher A Chapleau, Gaston D Calfa, Meredith C Lane, 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.
Nature Reviews. Disease Primers
|
March 25, 2025
Publisher Correction: Rett syndrome
Wendy A Gold, Alan K Percy, Jeffrey L Neul, et al.
Page
of 11
Search research articles
Search
Showing results (41-50 of 107) with videos related to
Sort By:
Page
of 11
Scientific Reports
|
December 9, 2016
From Function to Phenotype: Impaired DNA Binding and Clustering Correlates with Clinical Severity in Males with Missense Mutations in MECP2
Taimoor I Sheikh, Juan Ausió, Hannah Faghfoury, et al.
Pediatric Neurology
|
October 30, 2024
MECP2 Variants in Males: More Common than Previously Appreciated
Amitha Ananth, Cary Fu, Jeffrey L Neul, et al.
Frontiers in Integrative Neuroscience
|
March 13, 2020
Metabolic Signatures Differentiate Rett Syndrome From Unaffected Siblings
Jeffrey L Neul, Steven A Skinner, Fran Annese, et al.
Pediatric Neurology
|
March 29, 2017
Scoliosis in Rett Syndrome: Progression, Comorbidities, and Predictors
John T Killian, Jane B Lane, Hye-Seung Lee, et al.
The Journal of Pediatrics
|
September 24, 2009
Longevity in Rett syndrome: analysis of the North American Database
Russell S Kirby, Jane B Lane, Jerry Childers, 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.
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.
Neurobiology of Disease
|
May 16, 2009
Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations
Christopher A Chapleau, Gaston D Calfa, Meredith C Lane, 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.
Nature Reviews. Disease Primers
|
March 25, 2025
Publisher Correction: Rett syndrome
Wendy A Gold, Alan K Percy, Jeffrey L Neul, et al.
Page
of 11