Maithé Tauber

19PUBLICATIONS
58CO-AUTHORS
Nutrigenomics and personalised nutritionInfant and child healthNeonatologyEpigenetics (incl. genome methylation and epigenomics)Genetic immunology
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Publications (19)

|Mar 11, 2026
Circulating levels of ghrelin and hyperphagia in patients with rare genetic neurodevelopmental disorders.

Gwenaëlle Diene, Grégoire Benvegnu, Cathy Brochado

|Feb 05, 2026
Oxytocin in infants with Prader-Willi syndrome to improve dysphagia and disease trajectory.

Maithe Tauber, Gwenaelle Diene, Pascale Fichaux-Bourin

|Nov 13, 2025
Adherence and Growth Outcomes in a Large Cohort of Children Treated With Recombinant GH Using a Connected Auto-injector.

Michel Polak, Natacha Bouhours-Nouet, Paula van Dommelen

|Mar 02, 2025
Early oxytocin treatment in infants with Prader-Willi syndrome is safe and is associated with better endocrine, metabolic and behavioral outcomes.

Marion Valette, Gwenaelle Diene, Mélanie Glattard

|Dec 05, 2024
Cardiovascular autonomic dysfunction and sleep abnormalities in children with Prader-Willi syndrome.

Rachel Debs, Gwenaëlle Diene, Julie Cortadellas

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