David Hessl

Affiliations: 
Psychiatry and Behavioral Sciences University of California, Davis, Davis, CA 
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Hessl D, Mandujano Rojas K, Ferrer E, et al. (2023) FMR1 Carriers Report Executive Function Changes Prior to Fragile X-Associated Tremor/Ataxia Syndrome: A Longitudinal Study. Movement Disorders : Official Journal of the Movement Disorder Society
Tassone F, Protic D, Allen EG, et al. (2023) Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on Premutation. Cells. 12
Aishworiya R, Tak YE, Ponzini MD, et al. (2023) Adaptive, behavioral, and cognitive outcomes in individuals with fragile X syndrome with varying autism severity. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience
Hessl D, Rojas KM, Ferrer E, et al. (2023) A Longitudinal Study of Executive Function in Daily Life in Male Fragile X Premutation Carriers and Association with FXTAS Conversion. Medrxiv : the Preprint Server For Health Sciences
Zafarullah M, Li J, Salemi MR, et al. (2023) Blood Proteome Profiling Reveals Biomarkers and Pathway Alterations in Fragile X PM at Risk for Developing FXTAS. International Journal of Molecular Sciences. 24
Berry-Kravis E, Abbeduto L, Hagerman R, et al. (2023) Effects of AFQ056 on language learning in fragile X syndrome. The Journal of Clinical Investigation
Aishworiya R, Chi MH, Zafarullah M, et al. (2023) Intercorrelation of Molecular Biomarkers and Clinical Phenotype Measures in Fragile X Syndrome. Cells. 12
Coleman J, Thompson T, Riley K, et al. (2023) The comparison of expressed emotion of parents of individuals with fragile X syndrome to other intellectual disabilities. Journal of Applied Research in Intellectual Disabilities : Jarid
Shields R, Kaat A, Sansone S, et al. (2022) Sensitivity of the NIH Toolbox to Detect Cognitive Change in Individuals With Intellectual and Developmental Disability. Neurology
Tang SJ, Giri S, Pahlavan N, et al. (2022) Tophaceous gout of the nose in a male premutation carrier. Clinical Case Reports. 10: e6586
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