Hyperphagia in Prader–Willi syndrome: linking hypothalamic dysfunction to clinical assessment and management across the lifespan

Maithé Tauber, Gwenaëlle Diene, Christine Poitou, Charlotte Höybye, Evelien F. Gevers, Anthony P. Goldstone, Andrea M. Haqq, Yoon Hi Cho, Ashley H. Shoemaker, Janice L. Forster, Anthony Holland, Stephanie Brown, Laura de Graaff, Ann Manzardo, Assumpta Caixàs, Elena G. Bochukova, Paula Maguire, Dairine Dempsey, Jennifer Miller

Open source

DOI: 10.1186/s13023-026-04601-1
Published: 2026-10-05
Container: Orphanet Journal of Rare Diseases
Publisher: Springer Science and Business Media LLC
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1186/s13023-026-04601-1,
  title = {Hyperphagia in Prader–Willi syndrome: linking hypothalamic dysfunction to clinical assessment and management across the lifespan},
  author = {Maithé Tauber and Gwenaëlle Diene and Christine Poitou and Charlotte Höybye and Evelien F. Gevers and Anthony P. Goldstone and Andrea M. Haqq and Yoon Hi Cho and Ashley H. Shoemaker and Janice L. Forster and Anthony Holland and Stephanie Brown and Laura de Graaff and Ann Manzardo and Assumpta Caixàs and Elena G. Bochukova and Paula Maguire and Dairine Dempsey and Jennifer Miller},
  year = {2026},
  journal = {Orphanet Journal of Rare Diseases},
  doi = {10.1186/s13023-026-04601-1},
  url = {https://doi.org/10.1186/s13023-026-04601-1}
}

RIS

TY  - JOUR
TI  - Hyperphagia in Prader–Willi syndrome: linking hypothalamic dysfunction to clinical assessment and management across the lifespan
AU  - Maithé Tauber
AU  - Gwenaëlle Diene
AU  - Christine Poitou
AU  - Charlotte Höybye
AU  - Evelien F. Gevers
AU  - Anthony P. Goldstone
AU  - Andrea M. Haqq
AU  - Yoon Hi Cho
AU  - Ashley H. Shoemaker
AU  - Janice L. Forster
AU  - Anthony Holland
AU  - Stephanie Brown
AU  - Laura de Graaff
AU  - Ann Manzardo
AU  - Assumpta Caixàs
AU  - Elena G. Bochukova
AU  - Paula Maguire
AU  - Dairine Dempsey
AU  - Jennifer Miller
PY  - 2026
JO  - Orphanet Journal of Rare Diseases
DO  - 10.1186/s13023-026-04601-1
UR  - https://doi.org/10.1186/s13023-026-04601-1
ER  -

APA

Tauber, M., Diene, G., Poitou, C., Höybye, C., Gevers, E. F., Goldstone, A. P., Haqq, A. M., Cho, Y. H., Shoemaker, A. H., Forster, J. L., Holland, A., Brown, S., Graaff, L. D., Manzardo, A., Caixàs, A., Bochukova, E. G., Maguire, P., Dempsey, D., & Miller, J. (2026). Hyperphagia in Prader–Willi syndrome: linking hypothalamic dysfunction to clinical assessment and management across the lifespan. Orphanet Journal of Rare Diseases. https://doi.org/10.1186/s13023-026-04601-1

Source records

crossref · retrieved 2026-11-09T19:14:53.369Z