High levels of LIGHT/TNFSF14 in patients with Prader–Willi syndrome

PURPOSE/METHODS: Prader–Willi syndrome (PWS) is a rare genetic disorder displaying different clinical features, including obesity and bone impairment. LIGHT/TNFSF14 is a cytokine produced by immune cells affecting both fat and bone metabolism. The present study aimed to evaluate LIGHT serum levels i...

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Detalles Bibliográficos
Autores principales: Faienza, M. F., Brunetti, G., Fintini, D., Grugni, G., Wasniewska, M. G., Crinò, A., D’Amato, G., Piacente, L., Oranger, A., Dicarlo, M., Colucci, S., Grano, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10371899/
https://www.ncbi.nlm.nih.gov/pubmed/36917420
http://dx.doi.org/10.1007/s40618-023-02050-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10371899/
https://www.ncbi.nlm.nih.gov/pubmed/36917420
http://dx.doi.org/10.1007/s40618-023-02050-2

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