SAT-446 No Central Adrenal Insufficiency Found in Adults with Prader-Willi Syndrome Tested by Multiple-Dose Metyrapone Test

por Davidse, Kirsten, Rosenberg, Anna, Pellikaan, Karlijn, Donze, Stephany, Hokken-Koelega, Anita, de Graaff-Herder, Laura
Publicado 2019

Free Insulin-like Growth Factor (IGF)-I in Children with PWS

por Damen, Layla, Elizabeth, Melitza S. M., Donze, Stephany H., van den Berg, Sjoerd A. A., de Graaff, Laura C. G., Hokken-Koelega, Anita C. S.
Publicado 2022

Oxytocin in young children with Prader‐Willi syndrome: Results of a randomized, double‐blind, placebo‐controlled, crossover trial investigating 3 months of oxytocin

por Damen, Layla, Grootjen, Lionne N., Juriaans, Alicia F., Donze, Stephany H., Huisman, T. Martin, Visser, Jenny A., Delhanty, Patric J.D., Hokken‐Koelega, Anita C.S.
Publicado 2020

Evidence for Accelerated Biological Aging in Young Adults with Prader–Willi Syndrome

por Donze, Stephany H, Codd, Veryan, Damen, Layla, Goedegebuure, Wesley J, Denniff, Matthew, Samani, Nilesh J, van der Velden, Janiëlle A E M, Hokken-Koelega, Anita C S
Publicado 2019

Three years of growth hormone treatment in young adults with Prader-Willi syndrome: sustained positive effects on body composition

por Damen, Layla, Donze, Stephany H., Kuppens, Renske J., Bakker, Nienke E., de Graaff, Laura C. G., van der Velden, Janielle A. E. M., Hokken-Koelega, Anita C. S.
Publicado 2020

A Transcriptomic Signature of the Hypothalamic Response to Fasting and BDNF Deficiency in Prader-Willi Syndrome

por Bochukova, Elena G., Lawler, Katherine, Croizier, Sophie, Keogh, Julia M., Patel, Nisha, Strohbehn, Garth, Lo, Kitty K., Humphrey, Jack, Hokken-Koelega, Anita, Damen, Layla, Donze, Stephany, Bouret, Sebastien G., Plagnol, Vincent, Farooqi, I. Sadaf
Publicado 2018

Prevalence of growth hormone (GH) deficiency in previously GH‐treated young adults with Prader‐Willi syndrome

por Donze, Stephany H., Damen, Layla, van Alfen‐van der Velden, Janiëlle A. E. M., Bocca, Gianni, Finken, Martijn J. J., Hoorweg‐Nijman, Gera J. G., Jira, Petr E., van Leeuwen, Mariëtte, Hokken‐Koelega, Anita C. S.
Publicado 2019

Complementing the phenotypical spectrum of TUBA1A tubulinopathy and its role in early-onset epilepsies

por Schröter, Julian, Popp, Bernt, Brennenstuhl, Heiko, Döring, Jan H., Donze, Stephany H., Bijlsma, Emilia K., van Haeringen, Arie, Huhle, Dagmar, Jestaedt, Leonie, Merkenschlager, Andreas, Arelin, Maria, Gräfe, Daniel, Neuser, Sonja, Oates, Stephanie, Pal, Deb K., Parker, Michael J., Lemke, Johannes R., Hoffmann, Georg F., Kölker, Stefan, Harting, Inga, Syrbe, Steffen
Publicado 2022