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Kim M Cornish

Showing results (21-30 of 41) with videos related to

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Developmental Science|September 22, 2016
Visual attention and academic performance in children with developmental disabilities and behavioural attention deficitsHannah E Kirk, Kylie Gray, Deborah M Riby, et al.
Cerebellum (London, England)|April 30, 2016
Executive Dysfunction in Female FMR1 Premutation CarriersAnnie L Shelton, Kim M Cornish, Claudine M Kraan, et al.
Neurology|May 7, 2017
White matter microstructure, cognition, and molecular markers in fragile X premutation femalesAnnie L Shelton, Kim M Cornish, David Godler, et al.
Brain and Cognition|December 31, 2008
Lifespan changes in working memory in fragile X premutation malesKim M Cornish, Cary S Kogan, Lexin Li, et al.
Behavioural Brain Research|January 17, 2015
Delineation of the working memory profile in female FMR1 premutation carriers: the effect of cognitive load on ocular motor responsesAnnie L Shelton, Kim M Cornish, David E Godler, et al.
Plos One|February 24, 2018
β-glucuronidase use as a single internal control gene may confound analysis in FMR1 mRNA toxicity studiesClaudine M Kraan, Kim M Cornish, Quang M Bui, et al.
Autism : the International Journal of Research and Practice|June 30, 2016
The developmental trajectory of parent-report and objective sleep profiles in autism spectrum disorder: Associations with anxiety and bedtime routinesFay E Fletcher, Mistral D Foster-Owens, Russell Conduit, et al.
Developmental Science|April 17, 2013
The interplay between executive control and motor functioning in Williams syndromeDarren R Hocking, Daniel Thomas, Jasmine C Menant, et al.
Behavioral Sleep Medicine|June 3, 2016
The Association Between Anxiety Symptoms and Sleep in School-Aged Children: A Combined Insight From the Children's Sleep Habits Questionnaire and ActigraphyFay E Fletcher, Russell Conduit, Mistral D Foster-Owens, et al.
Neuroscience and Biobehavioral Reviews|January 29, 2013
Neurobehavioural evidence for the involvement of the FMR1 gene in female carriers of fragile X syndromeClaudine M Kraan, Darren R Hocking, John L Bradshaw, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Developmental Science|September 22, 2016
Visual attention and academic performance in children with developmental disabilities and behavioural attention deficitsHannah E Kirk, Kylie Gray, Deborah M Riby, et al.
Cerebellum (London, England)|April 30, 2016
Executive Dysfunction in Female FMR1 Premutation CarriersAnnie L Shelton, Kim M Cornish, Claudine M Kraan, et al.
Neurology|May 7, 2017
White matter microstructure, cognition, and molecular markers in fragile X premutation femalesAnnie L Shelton, Kim M Cornish, David Godler, et al.
Brain and Cognition|December 31, 2008
Lifespan changes in working memory in fragile X premutation malesKim M Cornish, Cary S Kogan, Lexin Li, et al.
Behavioural Brain Research|January 17, 2015
Delineation of the working memory profile in female FMR1 premutation carriers: the effect of cognitive load on ocular motor responsesAnnie L Shelton, Kim M Cornish, David E Godler, et al.
Plos One|February 24, 2018
β-glucuronidase use as a single internal control gene may confound analysis in FMR1 mRNA toxicity studiesClaudine M Kraan, Kim M Cornish, Quang M Bui, et al.
Autism : the International Journal of Research and Practice|June 30, 2016
The developmental trajectory of parent-report and objective sleep profiles in autism spectrum disorder: Associations with anxiety and bedtime routinesFay E Fletcher, Mistral D Foster-Owens, Russell Conduit, et al.
Developmental Science|April 17, 2013
The interplay between executive control and motor functioning in Williams syndromeDarren R Hocking, Daniel Thomas, Jasmine C Menant, et al.
Behavioral Sleep Medicine|June 3, 2016
The Association Between Anxiety Symptoms and Sleep in School-Aged Children: A Combined Insight From the Children's Sleep Habits Questionnaire and ActigraphyFay E Fletcher, Russell Conduit, Mistral D Foster-Owens, et al.
Neuroscience and Biobehavioral Reviews|January 29, 2013
Neurobehavioural evidence for the involvement of the FMR1 gene in female carriers of fragile X syndromeClaudine M Kraan, Darren R Hocking, John L Bradshaw, et al.
Pageof 5