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Elizabeth Berry

Showing results (201-210 of 312) with videos related to

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BMJ (Clinical Research Ed.)|January 26, 2002
Use of magnetic resonance angiography to select candidates with recently symptomatic carotid stenosis for surgery: systematic reviewMarie E Westwood, Steven Kelly, Elizabeth Berry, et al.
American Journal on Intellectual and Developmental Disabilities|August 26, 2025
Retrospective Reports of Skill Attainment and Loss in Phelan-McDermid SyndromeCristan Farmer, Ivy Giserman-Kiss, Ellora Mohanty, et al.
Science Advances|August 29, 2019
Data-driven phenotype discovery of <i>FMR1</i> premutation carriers in a population-based sampleArezoo Movaghar, David Page, Murray Brilliant, et al.
Journal of Lipid Research|July 24, 2024
Accumulation of alkyl-lysophosphatidylcholines in Niemann-Pick disease type C1Sonali Mishra, Pamela Kell, David Scherrer, et al.
Human Molecular Genetics|May 12, 2011
Altered zinc transport disrupts mitochondrial protein processing/import in fragile X-associated tremor/ataxia syndromeEleonora Napoli, Catherine Ross-Inta, Sarah Wong, et al.
Nature Reviews. Disease Primers|September 30, 2017
Fragile X syndromeRandi J Hagerman, Elizabeth Berry-Kravis, Heather Cody Hazlett, et al.
Gait & Posture|June 13, 2020
Normative database of spatiotemporal gait parameters using inertial sensors in typically developing children and young adultsStephanie Voss, Jessica Joyce, Alexandras Biskis, et al.
Neurology|March 29, 2019
Double-blind, randomized, placebo-controlled study of trofinetide in pediatric Rett syndromeDaniel G Glaze, Jeffrey L Neul, Walter E Kaufmann, et al.
Genome Medicine|December 25, 2012
FMR1 CGG allele size and prevalence ascertained through newborn screening in the United StatesFlora Tassone, Ka Pou Iong, Tzu-Han Tong, et al.
Nature Reviews. Drug Discovery|April 3, 2019
Discovering translational biomarkers in neurodevelopmental disordersMustafa Sahin, Stephanie R Jones, John A Sweeney, et al.
Pageof 32

Showing results (201-210 of 312) with videos related to

Sort By:
Pageof 32
BMJ (Clinical Research Ed.)|January 26, 2002
Use of magnetic resonance angiography to select candidates with recently symptomatic carotid stenosis for surgery: systematic reviewMarie E Westwood, Steven Kelly, Elizabeth Berry, et al.
American Journal on Intellectual and Developmental Disabilities|August 26, 2025
Retrospective Reports of Skill Attainment and Loss in Phelan-McDermid SyndromeCristan Farmer, Ivy Giserman-Kiss, Ellora Mohanty, et al.
Science Advances|August 29, 2019
Data-driven phenotype discovery of <i>FMR1</i> premutation carriers in a population-based sampleArezoo Movaghar, David Page, Murray Brilliant, et al.
Journal of Lipid Research|July 24, 2024
Accumulation of alkyl-lysophosphatidylcholines in Niemann-Pick disease type C1Sonali Mishra, Pamela Kell, David Scherrer, et al.
Human Molecular Genetics|May 12, 2011
Altered zinc transport disrupts mitochondrial protein processing/import in fragile X-associated tremor/ataxia syndromeEleonora Napoli, Catherine Ross-Inta, Sarah Wong, et al.
Nature Reviews. Disease Primers|September 30, 2017
Fragile X syndromeRandi J Hagerman, Elizabeth Berry-Kravis, Heather Cody Hazlett, et al.
Gait & Posture|June 13, 2020
Normative database of spatiotemporal gait parameters using inertial sensors in typically developing children and young adultsStephanie Voss, Jessica Joyce, Alexandras Biskis, et al.
Neurology|March 29, 2019
Double-blind, randomized, placebo-controlled study of trofinetide in pediatric Rett syndromeDaniel G Glaze, Jeffrey L Neul, Walter E Kaufmann, et al.
Genome Medicine|December 25, 2012
FMR1 CGG allele size and prevalence ascertained through newborn screening in the United StatesFlora Tassone, Ka Pou Iong, Tzu-Han Tong, et al.
Nature Reviews. Drug Discovery|April 3, 2019
Discovering translational biomarkers in neurodevelopmental disordersMustafa Sahin, Stephanie R Jones, John A Sweeney, et al.
Pageof 32