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David Hessl

Biographic Data

ID7380242
NAMEDavid Hessl
GIVEN NAMESDavid
FAMILY NAMEHessl
SIGNATUREHESSL D
AFFILIATIONSUniversity of California Davis Medical Center
ORCID0000-0002-3460-9805
VERIFIEDYes
TOTAL WORKS2
TOTAL CITATIONS0
WORKS AS AUTHOR2
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2021
LATEST PUBLICATION YEAR2021
H-INDEX0
  • 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…

No prominent works on this page.

  • 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 works) · Medicine (2 works) · Neuroscience (2 works) · Psychiatry (2 works) · Psychology (2 works) · Advanced battery technologies research (1 work) · Allele (1 work) · Ataxia (1 work) · Audiology (1 work) · Autism Spectrum Disorder Research (1 work)

Ethnos_APP • Open Source Project • MIT License • Frontend v2.0.0 • Privacy and Cookies • API Documentation: api.ethnos.app/docs • API Source Code: GitHub • DOI: 10.5281/zenodo.17049435 • Frontend Source Code: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae