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Flora Tassone

Showing results (131-140 of 348) with videos related to

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Human Genetics|September 3, 2010
Autoimmune disease in mothers with the FMR1 premutation is associated with seizures in their children with fragile X syndromeWeerasak Chonchaiya, Flora Tassone, Paul Ashwood, et al.
Cerebellum (London, England)|June 24, 2016
Aging in Fragile X Premutation CarriersReymundo Lozano, Naomi Saito, Dallas Reed, et al.
Archives of Neurology|July 11, 2007
Screen for excess FMR1 premutation alleles among males with parkinsonismJeremy Kraff, Hiu-Tung Tang, Roberto Cilia, et al.
Journal of Autism and Developmental Disorders|June 4, 2010
Brief report: Sensorimotor gating in idiopathic autism and autism associated with fragile X syndromeJennifer Yuhas, Lisa Cordeiro, Flora Tassone, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2012
AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndromeCarolyn M Yrigollen, Blythe Durbin-Johnson, Louise Gane, et al.
The Journal of Molecular Diagnostics : JMD|May 23, 2009
A quantitative ELISA assay for the fragile x mental retardation 1 proteinChristine Iwahashi, Flora Tassone, Randi J Hagerman, et al.
Brain : a Journal of Neurology|December 15, 2006
Amygdala dysfunction in men with the fragile X premutationDavid Hessl, Susan Rivera, Kami Koldewyn, et al.
The Journal of Molecular Diagnostics : JMD|November 1, 2005
An enhanced polymerase chain reaction assay to detect pre- and full mutation alleles of the fragile X mental retardation 1 geneAlessandro Saluto, Alessandro Brussino, Flora Tassone, et al.
Brain Sciences|June 14, 2020
Blood-Based Biomarkers Predictive of Metformin Target Engagement in Fragile X SyndromeMittal Jasoliya, Heather Bowling, Ignacio Cortina Petrasic, et al.
Journal of Neurodevelopmental Disorders|May 5, 2015
A cross-sectional analysis of orienting of visuospatial attention in child and adult carriers of the fragile X premutationLing M Wong, Naomi J Goodrich-Hunsaker, Yingratana A McLennan, et al.
Pageof 35

Showing results (131-140 of 348) with videos related to

Sort By:
Pageof 35
Human Genetics|September 3, 2010
Autoimmune disease in mothers with the FMR1 premutation is associated with seizures in their children with fragile X syndromeWeerasak Chonchaiya, Flora Tassone, Paul Ashwood, et al.
Cerebellum (London, England)|June 24, 2016
Aging in Fragile X Premutation CarriersReymundo Lozano, Naomi Saito, Dallas Reed, et al.
Archives of Neurology|July 11, 2007
Screen for excess FMR1 premutation alleles among males with parkinsonismJeremy Kraff, Hiu-Tung Tang, Roberto Cilia, et al.
Journal of Autism and Developmental Disorders|June 4, 2010
Brief report: Sensorimotor gating in idiopathic autism and autism associated with fragile X syndromeJennifer Yuhas, Lisa Cordeiro, Flora Tassone, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2012
AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndromeCarolyn M Yrigollen, Blythe Durbin-Johnson, Louise Gane, et al.
The Journal of Molecular Diagnostics : JMD|May 23, 2009
A quantitative ELISA assay for the fragile x mental retardation 1 proteinChristine Iwahashi, Flora Tassone, Randi J Hagerman, et al.
Brain : a Journal of Neurology|December 15, 2006
Amygdala dysfunction in men with the fragile X premutationDavid Hessl, Susan Rivera, Kami Koldewyn, et al.
The Journal of Molecular Diagnostics : JMD|November 1, 2005
An enhanced polymerase chain reaction assay to detect pre- and full mutation alleles of the fragile X mental retardation 1 geneAlessandro Saluto, Alessandro Brussino, Flora Tassone, et al.
Brain Sciences|June 14, 2020
Blood-Based Biomarkers Predictive of Metformin Target Engagement in Fragile X SyndromeMittal Jasoliya, Heather Bowling, Ignacio Cortina Petrasic, et al.
Journal of Neurodevelopmental Disorders|May 5, 2015
A cross-sectional analysis of orienting of visuospatial attention in child and adult carriers of the fragile X premutationLing M Wong, Naomi J Goodrich-Hunsaker, Yingratana A McLennan, et al.
Pageof 35