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Genes, Brain, and Behavior
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May 4, 2021
Safety and efficacy of genetic MECP2 supplementation in the R294X mouse model of Rett syndrome
Bridget E Collins, Jonathan K Merritt, Kirsty R Erickson, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
August 22, 2014
Low bone mineral mass is associated with decreased bone formation and diet in girls with Rett syndrome
Kathleen J Motil, Judy O Barrish, Jeffrey L Neul, et al.
Scientific Reports
|
August 24, 2017
Embryonic hindbrain patterning genes delineate distinct cardio-respiratory and metabolic homeostatic populations in the adult
Jenny J Sun, Teng-Wei Huang, Jeffrey L Neul, et al.
Journal of Neurodevelopmental Disorders
|
July 20, 2024
A clinical-translational review of sleep problems in neurodevelopmental disabilities
Sarika U Peters, Althea Robinson Shelton, Beth A Malow, et al.
Human Molecular Genetics
|
February 5, 2017
Methyl-CpG binding-protein 2 function in cholinergic neurons mediates cardiac arrhythmogenesis
José A Herrera, Christopher S Ward, Xander H T Wehrens, et al.
Journal of Child Neurology
|
June 26, 2025
Sleep Problems and Clinical Severity in Rett Syndrome
Sarika U Peters, Cary Fu, Althea Robinson Shelton, et al.
Annals of the Child Neurology Society
|
August 29, 2025
Symptom Onset in Classic Rett Syndrome: Analysis of Initial Clinical Severity Scale Entries
Alan K Percy, Jeffrey L Neul, Amitha Ananth, et al.
Human Molecular Genetics
|
May 30, 2020
Pharmacological read-through of R294X Mecp2 in a novel mouse model of Rett syndrome
Jonathan K Merritt, Bridget E Collins, Kirsty R Erickson, et al.
Journal of Autism and Developmental Disorders
|
August 8, 2013
Brief report: MECP2 mutations in people without Rett syndrome
Bernhard Suter, Diane Treadwell-Deering, Huda Y Zoghbi, et al.
Translational Science of Rare Diseases
|
April 24, 2018
When Rett syndrome is due to genes other than <i>MECP2</i>
Alan K Percy, Jane Lane, Fran Annese, et al.
Page
of 13
Search research articles
Search
Showing results (11-20 of 122) with videos related to
Sort By:
Page
of 13
Genes, Brain, and Behavior
|
May 4, 2021
Safety and efficacy of genetic MECP2 supplementation in the R294X mouse model of Rett syndrome
Bridget E Collins, Jonathan K Merritt, Kirsty R Erickson, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
August 22, 2014
Low bone mineral mass is associated with decreased bone formation and diet in girls with Rett syndrome
Kathleen J Motil, Judy O Barrish, Jeffrey L Neul, et al.
Scientific Reports
|
August 24, 2017
Embryonic hindbrain patterning genes delineate distinct cardio-respiratory and metabolic homeostatic populations in the adult
Jenny J Sun, Teng-Wei Huang, Jeffrey L Neul, et al.
Journal of Neurodevelopmental Disorders
|
July 20, 2024
A clinical-translational review of sleep problems in neurodevelopmental disabilities
Sarika U Peters, Althea Robinson Shelton, Beth A Malow, et al.
Human Molecular Genetics
|
February 5, 2017
Methyl-CpG binding-protein 2 function in cholinergic neurons mediates cardiac arrhythmogenesis
José A Herrera, Christopher S Ward, Xander H T Wehrens, et al.
Journal of Child Neurology
|
June 26, 2025
Sleep Problems and Clinical Severity in Rett Syndrome
Sarika U Peters, Cary Fu, Althea Robinson Shelton, et al.
Annals of the Child Neurology Society
|
August 29, 2025
Symptom Onset in Classic Rett Syndrome: Analysis of Initial Clinical Severity Scale Entries
Alan K Percy, Jeffrey L Neul, Amitha Ananth, et al.
Human Molecular Genetics
|
May 30, 2020
Pharmacological read-through of R294X Mecp2 in a novel mouse model of Rett syndrome
Jonathan K Merritt, Bridget E Collins, Kirsty R Erickson, et al.
Journal of Autism and Developmental Disorders
|
August 8, 2013
Brief report: MECP2 mutations in people without Rett syndrome
Bernhard Suter, Diane Treadwell-Deering, Huda Y Zoghbi, et al.
Translational Science of Rare Diseases
|
April 24, 2018
When Rett syndrome is due to genes other than <i>MECP2</i>
Alan K Percy, Jane Lane, Fran Annese, et al.
Page
of 13