Search research articles
Contact Us
Filters
Showing results (21-30 of 107) with videos related to
Page
of 11
Sort By:
Annals of the New York Academy of Sciences
|
November 1, 2017
Cocaine-Inhibited Neuronal Differentiation in NGF-Induced PC12 Cells and Altered C-fos Expression Are Reversed by C-fos Antisense Oligonucleotide<sup>a</sup>
Ditza A Zachor, John F Moore, Anne B Theibert, et al.
Journal of Neurodevelopmental Disorders
|
February 13, 2010
Variable phenotypic expression of a MECP2 mutation in a family
Kimberly Augenstein, Jane B Lane, Antony Horton, et al.
Degenerative Neurological and Neuromuscular Disease
|
July 17, 2020
MeCP2 in the regulation of neural activity: Rett syndrome pathophysiological perspectives
Vishnu Anand Cuddapah, Elvee Nwaobi Sinifunanya, Alan K Percy, et al.
Journal of Child Neurology
|
October 18, 2005
Rett syndrome: pathogenesis, diagnosis, strategies, therapies, and future research directions
Kathleen M Deidrick, Alan K Percy, N Carolyn Schanen, 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.
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.
Frontiers in Pediatrics
|
August 28, 2023
A review of the Rett Syndrome Behaviour Questionnaire and its utilization in the assessment of symptoms associated with Rett syndrome
Alan K Percy, Jeffrey L Neul, Timothy A Benke, et al.
Future Neurology
|
December 19, 2013
Recent Progress in Rett Syndrome and MeCP2 Dysfunction: Assessment of Potential Treatment Options
Christopher A Chapleau, Jane Lane, Jennifer Larimore, et al.
Neurobiology of Disease
|
February 17, 2009
Bdnf overexpression in hippocampal neurons prevents dendritic atrophy caused by Rett-associated MECP2 mutations
Jennifer L Larimore, Christopher A Chapleau, Shinichi Kudo, et al.
Mental Retardation and Developmental Disabilities Research Reviews
|
June 5, 2003
Certification in neurodevelopmental disabilities: the development of a new subspecialty and results of the initial examinations
Frederick B Palmer, Alan K Percy, Patricia Tivnan, et al.
Page
of 11
Search research articles
Search
Showing results (21-30 of 107) with videos related to
Sort By:
Page
of 11
Annals of the New York Academy of Sciences
|
November 1, 2017
Cocaine-Inhibited Neuronal Differentiation in NGF-Induced PC12 Cells and Altered C-fos Expression Are Reversed by C-fos Antisense Oligonucleotide<sup>a</sup>
Ditza A Zachor, John F Moore, Anne B Theibert, et al.
Journal of Neurodevelopmental Disorders
|
February 13, 2010
Variable phenotypic expression of a MECP2 mutation in a family
Kimberly Augenstein, Jane B Lane, Antony Horton, et al.
Degenerative Neurological and Neuromuscular Disease
|
July 17, 2020
MeCP2 in the regulation of neural activity: Rett syndrome pathophysiological perspectives
Vishnu Anand Cuddapah, Elvee Nwaobi Sinifunanya, Alan K Percy, et al.
Journal of Child Neurology
|
October 18, 2005
Rett syndrome: pathogenesis, diagnosis, strategies, therapies, and future research directions
Kathleen M Deidrick, Alan K Percy, N Carolyn Schanen, 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.
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.
Frontiers in Pediatrics
|
August 28, 2023
A review of the Rett Syndrome Behaviour Questionnaire and its utilization in the assessment of symptoms associated with Rett syndrome
Alan K Percy, Jeffrey L Neul, Timothy A Benke, et al.
Future Neurology
|
December 19, 2013
Recent Progress in Rett Syndrome and MeCP2 Dysfunction: Assessment of Potential Treatment Options
Christopher A Chapleau, Jane Lane, Jennifer Larimore, et al.
Neurobiology of Disease
|
February 17, 2009
Bdnf overexpression in hippocampal neurons prevents dendritic atrophy caused by Rett-associated MECP2 mutations
Jennifer L Larimore, Christopher A Chapleau, Shinichi Kudo, et al.
Mental Retardation and Developmental Disabilities Research Reviews
|
June 5, 2003
Certification in neurodevelopmental disabilities: the development of a new subspecialty and results of the initial examinations
Frederick B Palmer, Alan K Percy, Patricia Tivnan, et al.
Page
of 11