Early oxytocin treatment in infants with Prader–Willi syndrome is safe and is associated with better endocrine, metabolic and behavioral outcomes

Authors

Gwénaëlle Diene (ORCID: https://orcid.org/0009-0003-8970-0088)
Grégoire Benvegnu (ORCID: https://orcid.org/0000-0003-0275-7245)
Mélanie Glattard
Catherine Arnaud (ORCID: https://orcid.org/0000-0002-4002-802X)
Marion Valette (ORCID: https://orcid.org/0000-0002-2113-824X)
Jean‐Pierre Salles (ORCID: https://orcid.org/0000-0002-0941-8951)
M. Tauber (ORCID: https://orcid.org/0000-0002-0363-7862)
Pierre Payoux (ORCID: https://orcid.org/0000-0002-1374-1620)
Sandy Faye
Sophie Çabal
Julie Cortadellas
Kader Boulanouar
Catherine Molinas

Institutions

Centre National de la Recherche Scientifique (FR)
Université Toulouse III - Paul Sabatier (FR)
Inserm (FR)
Université Fédérale de Toulouse Midi-Pyrénées (FR)
Centre Hospitalier Universitaire de Toulouse (FR)
Hôpital Purpan (FR)
Clinique Pasteur (FR)
Hôpital des Enfants (FR)

Publication Details

Journal: Orphanet Journal of Rare Diseases
Published: 2025-03-01
DOI: https://doi.org/10.1186/s13023-025-03560-3
Citations: 6
Primary Topic: Genetic Syndromes and Imprinting
Type: article
Field-Weighted Citation Impact: 10.90

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article

Early oxytocin treatment in infants with Prader–Willi syndrome is safe and is associated with better endocrine, metabolic and behavioral outcomes

Gwénaëlle Diene, Grégoire Benvegnu, Mélanie Glattard, Catherine Arnaud et al.

Mar 1, 2025

6 citations

Orphanet Journal of Rare Diseases

Genetic Syndromes and Imprinting

10.90

article

Early oxytocin treatment in infants with Prader–Willi syndrome is safe and is associated with better endocrine, metabolic and behavioral outcomes

Gwénaëlle Diene, Grégoire Benvegnu, Mélanie Glattard, Catherine Arnaud, Marion Valette, Jean‐Pierre Salles, M. Tauber, Pierre Payoux, Sandy Faye, Sophie Çabal, Julie Cortadellas, Kader Boulanouar, Catherine Molinas

March 1, 2025article en

6 citations

Abstract

No abstract available for this paper.

Orphanet Journal of Rare DiseasesVol. 20(1)

Centre National de la Recherche Scientifique (FR), Université Toulouse III - Paul Sabatier (FR), Inserm (FR), Université Fédérale de Toulouse Midi-Pyrénées (FR), Centre Hospitalier Universitaire de Toulouse (FR), Hôpital Purpan (FR), Clinique Pasteur (FR), Hôpital des Enfants (FR)

Quality Education

Openalex Percentile: Top 2%

Genetic Syndromes and Imprinting

10.90

DOI Open Access PDF OpenAlex

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