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Elizabeth Berry-Kravis

Showing results (81-90 of 265) with videos related to

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Neurology. Genetics|August 2, 2018
<i>ASFMR1</i> splice variant: A predictor of fragile X-associated tremor/ataxia syndromePadmaja Vittal, Shrikant Pandya, Kevin Sharp, et al.
Plos One|January 18, 2019
Effects of mavoglurant on visual attention and pupil reactivity while viewing photographs of faces in Fragile X SyndromeDavid Hessl, Danielle Harvey, Stephanie Sansone, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 16, 2013
Clinical features of neurodegeneration with brain iron accumulation due to a C19orf12 gene mutationJennifer G Goldman, Sheila R Eichenseer, Elizabeth Berry-Kravis, et al.
Physiology & Behavior|November 26, 2019
Physiological regulation and social-emotional processing in female carriers of the FMR1 premutationMolly Winston, Kritika Nayar, Abigail L Hogan, et al.
Frontiers in Genetics|February 26, 2021
A Unique Visual Attention Profile Associated With the <i>FMR1</i> PremutationMolly Winston, Kritika Nayar, Emily Landau, et al.
Cerebellum (London, England)|May 28, 2021
Characterization of the Cerebrospinal Fluid Proteome in Patients with Fragile X-Associated Tremor/Ataxia SyndromeDiana A Abbasi, Thu T A Nguyen, Deborah A Hall, et al.
Neurobiology of Aging|June 25, 2014
Fragile X gene expansions are not associated with dementiaDeborah A Hall, David A Bennett, Christopher M Filley, et al.
Cerebellum (London, England)|September 10, 2021
Correction to: Characterization of the Cerebrospinal Fluid Proteome in Patients with Fragile X-Associated Tremor/Ataxia SyndromeDiana A Abbasi, Thu T A Nguyen, Deborah A Hall, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 26, 2023
Antisense oligonucleotide rescue of CGG expansion-dependent <i>FMR1</i> mis-splicing in fragile X syndrome restores FMRPSneha Shah, Kevin J Sharp, Sithara Raju Ponny, et al.
Pediatrics|October 8, 2014
Fragile X syndrome: a review of associated medical problemsSharon A Kidd, Ave Lachiewicz, Deborah Barbouth, et al.
Pageof 27

Showing results (81-90 of 265) with videos related to

Sort By:
Pageof 27
Neurology. Genetics|August 2, 2018
<i>ASFMR1</i> splice variant: A predictor of fragile X-associated tremor/ataxia syndromePadmaja Vittal, Shrikant Pandya, Kevin Sharp, et al.
Plos One|January 18, 2019
Effects of mavoglurant on visual attention and pupil reactivity while viewing photographs of faces in Fragile X SyndromeDavid Hessl, Danielle Harvey, Stephanie Sansone, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 16, 2013
Clinical features of neurodegeneration with brain iron accumulation due to a C19orf12 gene mutationJennifer G Goldman, Sheila R Eichenseer, Elizabeth Berry-Kravis, et al.
Physiology & Behavior|November 26, 2019
Physiological regulation and social-emotional processing in female carriers of the FMR1 premutationMolly Winston, Kritika Nayar, Abigail L Hogan, et al.
Frontiers in Genetics|February 26, 2021
A Unique Visual Attention Profile Associated With the <i>FMR1</i> PremutationMolly Winston, Kritika Nayar, Emily Landau, et al.
Cerebellum (London, England)|May 28, 2021
Characterization of the Cerebrospinal Fluid Proteome in Patients with Fragile X-Associated Tremor/Ataxia SyndromeDiana A Abbasi, Thu T A Nguyen, Deborah A Hall, et al.
Neurobiology of Aging|June 25, 2014
Fragile X gene expansions are not associated with dementiaDeborah A Hall, David A Bennett, Christopher M Filley, et al.
Cerebellum (London, England)|September 10, 2021
Correction to: Characterization of the Cerebrospinal Fluid Proteome in Patients with Fragile X-Associated Tremor/Ataxia SyndromeDiana A Abbasi, Thu T A Nguyen, Deborah A Hall, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 26, 2023
Antisense oligonucleotide rescue of CGG expansion-dependent <i>FMR1</i> mis-splicing in fragile X syndrome restores FMRPSneha Shah, Kevin J Sharp, Sithara Raju Ponny, et al.
Pediatrics|October 8, 2014
Fragile X syndrome: a review of associated medical problemsSharon A Kidd, Ave Lachiewicz, Deborah Barbouth, et al.
Pageof 27