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David Hessl

Datos Biográficos

ID7380242
NOMBREDavid Hessl
NOMBRESDavid
APELLIDOHessl
FIRMAHESSL D
AFILIACIONESUniversity of California Davis Medical Center
ORCID0000-0002-3460-9805
VERIFICADOSí
TOTAL DE OBRAS2
TOTAL DE CITAS0
OBRAS COMO AUTOR2
OBRAS COMO EDITOR0
PRIMER AÑO DE PUBLICACIÓN2021
AÑO MÁS RECIENTE DE PUBLICACIÓN2021
ÍNDICE H0
  • EEG Signal Complexity Is Reduced During Resting-State in Fragile X Syndrome

    Open Access•Mélodie Proteau-Lemieux, Inga Sophia Knoth et al.•ARTICLE•Frontiers in Psychiatry•2021

    Introduction: Fragile X syndrome (FXS) is a genetic disorder caused by a mutation of the fragile X mental retardation 1 gene ( FMR1 ). FXS is associated with neurophysiological abnormalities, including cortical hyperexcitability. Alterations in electroencephalogram (EEG) resting-state power spectral density (PSD) are well-defined in FXS and were found to be linked to neurodevelopmental delays. Whether non-linear dynamics of the brain signal are a…

  • Metabolomic Biomarkers Are Associated With Area of the Pons in Fragile X Premutation Carriers at Risk for Developing FXTAS

    Open Access•Marwa Zafarullah, Blythe Durbin‐Johnson et al.•ARTICLE•Frontiers in Psychiatry•2021

    Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late adult-onset neurodegenerative disorder that affects movement and cognition in male and female carriers of a premutation allele (55-200 CGG repeats; PM) in the fragile X mental retardation ( FMR1 ) gene. It is currently unknown how the observed brain changes are associated with metabolic signatures in individuals who develop the disorder over time. The primary objective of this study wa…

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  • EEG Signal Complexity Is Reduced During Resting-State in Fragile X Syndrome

    Open Access•Mélodie Proteau-Lemieux, Inga Sophia Knoth et al.•ARTICLE•Frontiers in Psychiatry•2021

    Introduction: Fragile X syndrome (FXS) is a genetic disorder caused by a mutation of the fragile X mental retardation 1 gene ( FMR1 ). FXS is associated with neurophysiological abnormalities, including cortical hyperexcitability. Alterations in electroencephalogram (EEG) resting-state power spectral density (PSD) are well-defined in FXS and were found to be linked to neurodevelopmental delays. Whether non-linear dynamics of the brain signal are a…

  • Metabolomic Biomarkers Are Associated With Area of the Pons in Fragile X Premutation Carriers at Risk for Developing FXTAS

    Open Access•Marwa Zafarullah, Blythe Durbin‐Johnson et al.•ARTICLE•Frontiers in Psychiatry•2021

    Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late adult-onset neurodegenerative disorder that affects movement and cognition in male and female carriers of a premutation allele (55-200 CGG repeats; PM) in the fragile X mental retardation ( FMR1 ) gene. It is currently unknown how the observed brain changes are associated with metabolic signatures in individuals who develop the disorder over time. The primary objective of this study wa…

Genetics and Neurodevelopmental Disorders (2 obras) · Medicine (2 obras) · Neuroscience (2 obras) · Psychiatry (2 obras) · Psychology (2 obras) · Advanced battery technologies research (1 obra) · Allele (1 obra) · Ataxia (1 obra) · Audiology (1 obra) · Autism Spectrum Disorder Research (1 obra)

Ethnos_APP • Proyecto Open Source • Licencia MIT • Frontend v2.0.0 • Privacidad y Cookies • Documentación de la API: api.ethnos.app/docs • Código de la API: GitHub • DOI: 10.5281/zenodo.17049435 • Código del Frontend: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae