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Elizabeth Berry

Showing results (141-150 of 312) with videos related to

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Frontiers in Molecular Neuroscience|April 13, 2018
Utility of the Hebb-Williams Maze Paradigm for Translational Research in Fragile X Syndrome: A Direct Comparison of Mice and HumansIsabelle Boutet, Charles A Collin, Lindsey S MacLeod, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 14, 2011
FMR1 gray-zone alleles: association with Parkinson's disease in women?Deborah A Hall, Elizabeth Berry-Kravis, Wenting Zhang, et al.
Psychopharmacology|November 1, 2013
The challenges of clinical trials in fragile X syndromeSébastien Jacquemont, Elizabeth Berry-Kravis, Randi Hagerman, et al.
Journal of the American Academy of Dermatology|March 27, 2026
Quantitative versus qualitative risk framing in patient decision aids for dysplastic nevi: A randomized A/B testing studyJaclyn N Roland-McGowan, Oscar M Ose, Yun Yu, et al.
Cerebellum (London, England)|March 13, 2015
Characterization and Early Detection of Balance Deficits in Fragile X Premutation Carriers With and Without Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS)Joan A O'Keefe, Erin Robertson-Dick, Emily J Dunn, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 26, 2025
Depression Symptom Trajectories in Mothers With the FMR1 Premutation Vary by CGG Repeat Length: A Longitudinal Study of 73 Women Spanning 20-75 Years of AgeJessica Klusek, Lauren Jenner, Abigail L Hogan, et al.
Molecular Genetics and Metabolism|January 13, 2026
Characterization of liver disease in a cohort of individuals with Niemann-Pick Disease, Type C1Neena Agrawal, Simona Bianconi, Rebecca Jaeger, et al.
Movement Disorders Clinical Practice|October 12, 2020
Prodromal Markers of Upper Limb Deficits in <i>FMR1</i> Premutation Carriers and Quantitative Outcome Measures for Future Clinical Trials in Fragile X-associated Tremor/Ataxia SyndromeJoan A O'Keefe, Deborah Bang, Erin E Robertson, et al.
Scientific Reports|November 21, 2022
The association between expressive language skills and adaptive behavior in individuals with Down syndromeLaura Del Hoyo Soriano, Jennifer Catalina Villarreal, Audra Sterling, et al.
Pediatrics|July 15, 2015
Maternal Consequences of the Detection of Fragile X Carriers in Newborn ScreeningDonald B Bailey, Anne Wheeler, Elizabeth Berry-Kravis, et al.
Pageof 32

Showing results (141-150 of 312) with videos related to

Sort By:
Pageof 32
Frontiers in Molecular Neuroscience|April 13, 2018
Utility of the Hebb-Williams Maze Paradigm for Translational Research in Fragile X Syndrome: A Direct Comparison of Mice and HumansIsabelle Boutet, Charles A Collin, Lindsey S MacLeod, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 14, 2011
FMR1 gray-zone alleles: association with Parkinson's disease in women?Deborah A Hall, Elizabeth Berry-Kravis, Wenting Zhang, et al.
Psychopharmacology|November 1, 2013
The challenges of clinical trials in fragile X syndromeSébastien Jacquemont, Elizabeth Berry-Kravis, Randi Hagerman, et al.
Journal of the American Academy of Dermatology|March 27, 2026
Quantitative versus qualitative risk framing in patient decision aids for dysplastic nevi: A randomized A/B testing studyJaclyn N Roland-McGowan, Oscar M Ose, Yun Yu, et al.
Cerebellum (London, England)|March 13, 2015
Characterization and Early Detection of Balance Deficits in Fragile X Premutation Carriers With and Without Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS)Joan A O'Keefe, Erin Robertson-Dick, Emily J Dunn, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 26, 2025
Depression Symptom Trajectories in Mothers With the FMR1 Premutation Vary by CGG Repeat Length: A Longitudinal Study of 73 Women Spanning 20-75 Years of AgeJessica Klusek, Lauren Jenner, Abigail L Hogan, et al.
Molecular Genetics and Metabolism|January 13, 2026
Characterization of liver disease in a cohort of individuals with Niemann-Pick Disease, Type C1Neena Agrawal, Simona Bianconi, Rebecca Jaeger, et al.
Movement Disorders Clinical Practice|October 12, 2020
Prodromal Markers of Upper Limb Deficits in <i>FMR1</i> Premutation Carriers and Quantitative Outcome Measures for Future Clinical Trials in Fragile X-associated Tremor/Ataxia SyndromeJoan A O'Keefe, Deborah Bang, Erin E Robertson, et al.
Scientific Reports|November 21, 2022
The association between expressive language skills and adaptive behavior in individuals with Down syndromeLaura Del Hoyo Soriano, Jennifer Catalina Villarreal, Audra Sterling, et al.
Pediatrics|July 15, 2015
Maternal Consequences of the Detection of Fragile X Carriers in Newborn ScreeningDonald B Bailey, Anne Wheeler, Elizabeth Berry-Kravis, et al.
Pageof 32