Marion Valette
Toulouse, 31024, France
Last Updated: 09/26/2026
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Found 21 publications
Circulating levels of ghrelin and hyperphagia in patients with rare genetic neurodevelopmental disorders.
Journal: The Journal of clinical endocrinology and metabolism
Published: December 08, 2025
Circulating levels of ghrelin and hyperphagia in patients with rare genetic neurodevelopmental disorders.
Journal: The Journal of clinical endocrinology and metabolism
Published: December 08, 2025
Early neurodevelopmental brain perfusion abnormalities and functional connectivity findings in infants with Prader-Willi syndrome.
Journal: Journal of neurodevelopmental disorders
Published: October 14, 2025
Oxytocin in infants with Prader-Willi syndrome to improve dysphagia and disease trajectory.
Journal: Orphanet journal of rare diseases
Published: September 19, 2025
Behavior Regulation Abilities in Children With Prader-Willi Syndrome and Their Impact on Daily Life: At the Crossroads of Cognitive and Emotional Development.
Journal: Journal of autism and developmental disorders
Published: September 16, 2025
Isolation of adipose stromal cells from blood using a two-step microfluidic platform ASCfinder.
Journal: Scientific reports
Published: November 18, 2024
Early oxytocin treatment in infants with Prader-Willi syndrome is safe and is associated with better endocrine, metabolic and behavioral outcomes.
Journal: Orphanet journal of rare diseases
Published: June 21, 2024
Food socialization of children with Prader-Willi syndrome: an interdisciplinary problematization.
Journal: Frontiers in nutrition
Published: March 02, 2023
Impact of Deprivation on Obesity in Children with PWS.
Journal: Journal of clinical medicine
Published: February 15, 2022
Is ghrelin a biomarker of early-onset scoliosis in children with Prader-Willi syndrome?
Journal: Orphanet journal of rare diseases
Published: March 31, 2021
Last Updated: 09/26/2026