Oxytocin in infants with Prader-Willi syndrome to improve dysphagia and disease trajectory.
- DOI
- 10.1186/s13023-026-04214-8
- Published
- 2026 Feb 4
- Container
- Orphanet journal of rare diseases
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1186/s13023-026-04214-8,
title = {Oxytocin in infants with Prader-Willi syndrome to improve dysphagia and disease trajectory.},
author = {Tauber M and Diene G and Fichaux-Bourin P and Pinto G and Gueorguieva I and Nicolino M and Reynaud R and Bernoux D and Beauloye V and Abrahimians EM and Kiewert C and Payoux P and Cabal S and Molinas C and Glattard M and Viaux-Savelon S and Guedeney A and Cohen D and Arnaud C and Valette M},
year = {2026},
journal = {Orphanet journal of rare diseases},
doi = {10.1186/s13023-026-04214-8},
url = {https://doi.org/10.1186/s13023-026-04214-8}
}RIS
TY - JOUR TI - Oxytocin in infants with Prader-Willi syndrome to improve dysphagia and disease trajectory. AU - Tauber M AU - Diene G AU - Fichaux-Bourin P AU - Pinto G AU - Gueorguieva I AU - Nicolino M AU - Reynaud R AU - Bernoux D AU - Beauloye V AU - Abrahimians EM AU - Kiewert C AU - Payoux P AU - Cabal S AU - Molinas C AU - Glattard M AU - Viaux-Savelon S AU - Guedeney A AU - Cohen D AU - Arnaud C AU - Valette M PY - 2026 JO - Orphanet journal of rare diseases DO - 10.1186/s13023-026-04214-8 UR - https://doi.org/10.1186/s13023-026-04214-8 ER -
APA
M, T., G, D., P, F., G, P., I, G., M, N., R, R., D, B., V, B., EM, A., C, K., P, P., S, C., C, M., M, G., S, V., A, G., D, C., C, A., & M, V. (2026). Oxytocin in infants with Prader-Willi syndrome to improve dysphagia and disease trajectory.. Orphanet journal of rare diseases. https://doi.org/10.1186/s13023-026-04214-8
Source records
- pubmed · retrieved 2026-09-25T21:26:55.363Z