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Journal of Neuropathology and Experimental Neurology
|
July 4, 2024
Accumulation of TMEM106B C-terminal fragments in Niemann-Pick type C disease
Ruth D Azaria, Sean P Ferris, Randy S Tashjian, et al.
Plos One
|
July 27, 2019
Language processing skills linked to FMR1 variation: A study of gaze-language coordination during rapid automatized naming among women with the FMR1 premutation
Kritika Nayar, Walker McKinney, Abigail L Hogan, et al.
Journal of Proteome Research
|
August 14, 2020
Optimization of Protocols for Detection of De Novo Protein Synthesis in Whole Blood Samples via Azide-Alkyne Cycloaddition
Heather L Bowling, Amanda Kasper, Chhaya Patole, et al.
Pediatrics
|
August 18, 2017
FORWARD: A Registry and Longitudinal Clinical Database to Study Fragile X Syndrome
Stephanie L Sherman, Sharon A Kidd, Catharine Riley, et al.
Neurobiology of Disease
|
May 19, 2026
Cerebellar GABA and executive function among adult female carriers of the fragile X messenger ribonucleoprotein 1 premutation: a pilot study to examine neural underpinnings of the clinical phenotype
Roslyn Harold, Roma Kamat, Wei Siong Neo, et al.
Journal of Neurodevelopmental Disorders
|
June 16, 2017
Arbaclofen in fragile X syndrome: results of phase 3 trials
Elizabeth Berry-Kravis, Randi Hagerman, Jeannie Visootsak, et al.
Journal of Autism and Developmental Disorders
|
October 6, 2011
Psychometric study of the Aberrant Behavior Checklist in Fragile X Syndrome and implications for targeted treatment
Stephanie M Sansone, Keith F Widaman, Scott S Hall, et al.
Journal of Neurodevelopmental Disorders
|
September 8, 2016
The NIH Toolbox Cognitive Battery for intellectual disabilities: three preliminary studies and future directions
David Hessl, Stephanie M Sansone, Elizabeth Berry-Kravis, et al.
Pediatric Neurology
|
July 15, 2020
A Double-Blind, Randomized, Placebo-Controlled Clinical Study of Trofinetide in the Treatment of Fragile X Syndrome
Elizabeth Berry-Kravis, Joseph P Horrigan, Nicole Tartaglia, et al.
Science Advances
|
August 29, 2019
Data-driven phenotype discovery of <i>FMR1</i> premutation carriers in a population-based sample
Arezoo Movaghar, David Page, Murray Brilliant, et al.
Page
of 27
Search research articles
Search
Showing results (151-160 of 265) with videos related to
Sort By:
Page
of 27
Journal of Neuropathology and Experimental Neurology
|
July 4, 2024
Accumulation of TMEM106B C-terminal fragments in Niemann-Pick type C disease
Ruth D Azaria, Sean P Ferris, Randy S Tashjian, et al.
Plos One
|
July 27, 2019
Language processing skills linked to FMR1 variation: A study of gaze-language coordination during rapid automatized naming among women with the FMR1 premutation
Kritika Nayar, Walker McKinney, Abigail L Hogan, et al.
Journal of Proteome Research
|
August 14, 2020
Optimization of Protocols for Detection of De Novo Protein Synthesis in Whole Blood Samples via Azide-Alkyne Cycloaddition
Heather L Bowling, Amanda Kasper, Chhaya Patole, et al.
Pediatrics
|
August 18, 2017
FORWARD: A Registry and Longitudinal Clinical Database to Study Fragile X Syndrome
Stephanie L Sherman, Sharon A Kidd, Catharine Riley, et al.
Neurobiology of Disease
|
May 19, 2026
Cerebellar GABA and executive function among adult female carriers of the fragile X messenger ribonucleoprotein 1 premutation: a pilot study to examine neural underpinnings of the clinical phenotype
Roslyn Harold, Roma Kamat, Wei Siong Neo, et al.
Journal of Neurodevelopmental Disorders
|
June 16, 2017
Arbaclofen in fragile X syndrome: results of phase 3 trials
Elizabeth Berry-Kravis, Randi Hagerman, Jeannie Visootsak, et al.
Journal of Autism and Developmental Disorders
|
October 6, 2011
Psychometric study of the Aberrant Behavior Checklist in Fragile X Syndrome and implications for targeted treatment
Stephanie M Sansone, Keith F Widaman, Scott S Hall, et al.
Journal of Neurodevelopmental Disorders
|
September 8, 2016
The NIH Toolbox Cognitive Battery for intellectual disabilities: three preliminary studies and future directions
David Hessl, Stephanie M Sansone, Elizabeth Berry-Kravis, et al.
Pediatric Neurology
|
July 15, 2020
A Double-Blind, Randomized, Placebo-Controlled Clinical Study of Trofinetide in the Treatment of Fragile X Syndrome
Elizabeth Berry-Kravis, Joseph P Horrigan, Nicole Tartaglia, et al.
Science Advances
|
August 29, 2019
Data-driven phenotype discovery of <i>FMR1</i> premutation carriers in a population-based sample
Arezoo Movaghar, David Page, Murray Brilliant, et al.
Page
of 27