Improved Mental and Motor Development During 3 Years of GH Treatment in Very Young Children With Prader-Willi Syndrome
Donze, Stephany H, Damen, Layla, Mahabier, Eva F, Hokken-Koelega, Anita C S
Published in The journal of clinical endocrinology and metabolism (01.10.2018)
Published in The journal of clinical endocrinology and metabolism (01.10.2018)
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Journal Article
A Transcriptomic Signature of the Hypothalamic Response to Fasting and BDNF Deficiency in Prader-Willi Syndrome
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
Published in Cell reports (Cambridge) (27.03.2018)
Published in Cell reports (Cambridge) (27.03.2018)
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Journal Article
Oxytocin in young children with Prader‐Willi syndrome: Results of a randomized, double‐blind, placebo‐controlled, crossover trial investigating 3 months of oxytocin
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.
Published in Clinical endocrinology (Oxford) (01.05.2021)
Published in Clinical endocrinology (Oxford) (01.05.2021)
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Journal Article
Effects of 8 years of growth hormone treatment on scoliosis in children with Prader–Willi syndrome
Grootjen, Lionne N, Rutges, Joost P H J, Damen, Layla, Donze, Stephany H, Juriaans, Alicia F, Kerkhof, Gerthe F, Hokken-Koelega, Anita C S
Published in European journal of endocrinology (21.05.2021)
Published in European journal of endocrinology (21.05.2021)
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Journal Article
Three years of growth hormone treatment in young adults with Prader-Willi syndrome: sustained positive effects on body composition
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
Published in Orphanet journal of rare diseases (24.06.2020)
Published in Orphanet journal of rare diseases (24.06.2020)
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Journal Article
Novel Clinical Criteria Allow Detection of Short Stature Homeobox-Containing Gene Haploinsufficiency Caused by Either Gene or Enhancer Region Defects
Joustra, Sjoerd D., Kamp, Gerdine A., Stalman, Susanne E., Donze, Stephany H., Losekoot, Monique, Kant, Sarina G., de Bruin, Christiaan, Oostdijk, Wilma, Wit, Jan M.
Published in Hormone research in paediatrics (01.06.2020)
Published in Hormone research in paediatrics (01.06.2020)
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Journal Article
Sleep-Related Breathing Disorders in Young Adults With Prader-Willi Syndrome: A Placebo-Controlled, Crossover GH Trial
Donze, Stephany H, de Weerd, Al W, van den Bossche, Renilde A S, Joosten, Koen F M, Hokken-Koelega, Anita C S
Published in The journal of clinical endocrinology and metabolism (01.09.2019)
Published in The journal of clinical endocrinology and metabolism (01.09.2019)
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Journal Article
Limited additional value of karyotyping cultured amniotic fluid cell colonies in addition to microarray on uncultured cells for confirmation of abnormal non-invasive prenatal testing results
Donze, Stephany H, Srebniak, Malgorzata I, Diderich, Karin E M, van den Born, Myrthe, Galjaard, Robert-Jan, Govaerts, Lutgarde C P, van der Schoot, Vyne, Knapen, Maarten F C M, Joosten, Marieke, Van Opstal, Diane
Published in Prenatal diagnosis (01.04.2024)
Published in Prenatal diagnosis (01.04.2024)
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Journal Article
Complementing the phenotypical spectrum of TUBA1A tubulinopathy and its role in early-onset epilepsies
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
Published in European journal of human genetics : EJHG (01.03.2022)
Published in European journal of human genetics : EJHG (01.03.2022)
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Journal Article
Bone mineral density during 3 years of growth hormone in previously GH-treated young adults with PWS
Damen, Layla, Grootjen, Lionne N, Donze, Stephany H, de Graaff, Laura C G, van der Velden, Janielle A E M, Hokken-Koelega, Anita C S
Published in European journal of endocrinology (01.06.2021)
Published in European journal of endocrinology (01.06.2021)
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Journal Article
Evidence for Accelerated Biological Aging in Young Adults with Prader–Willi Syndrome
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
Published in The journal of clinical endocrinology and metabolism (01.06.2020)
Published in The journal of clinical endocrinology and metabolism (01.06.2020)
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Journal Article
Bone mineral density in young adults with Prader‐Willi syndrome: A randomized, placebo‐controlled, crossover GH trial
Donze, Stephany H., Kuppens, Renske J., Bakker, Nienke E., van Alfen‐van der Velden, Janiëlle A.E.M., Hokken‐Koelega, Anita C.S.
Published in Clinical endocrinology (Oxford) (01.06.2018)
Published in Clinical endocrinology (Oxford) (01.06.2018)
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Journal Article
Three years of growth hormone treatment in young adults with Prader‐Willi Syndrome previously treated with growth hormone in childhood: Effects on glucose homeostasis and metabolic syndrome
Damen, Layla, Grootjen, Lionne N., Donze, Stephany H., Juriaans, Alicia F., Graaff, Laura C. G., Velden, Janielle A.E.M., Hokken‐Koelega, Anita C. S.
Published in Clinical endocrinology (Oxford) (01.10.2020)
Published in Clinical endocrinology (Oxford) (01.10.2020)
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Journal Article
Beneficial Effects of GH in Young Adults With Prader-Willi Syndrome: A 2-Year Crossover Trial
Kuppens, Renske J, Bakker, Nienke E, Siemensma, Elbrich P. C, Tummers-de Lind van Wijngaarden, Roderick F. A, Donze, Stephany H, Festen, Dederieke A. M, van Alfen-van der Velden, Janielle A. E. M, Stijnen, Theo, Hokken-Koelega, Anita C. S
Published in The journal of clinical endocrinology and metabolism (01.11.2016)
Published in The journal of clinical endocrinology and metabolism (01.11.2016)
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Journal Article
Prevalence of growth hormone (GH) deficiency in previously GH‐treated young adults with Prader‐Willi syndrome
Donze, Stephany H., Damen, Layla, Alfen‐van der Velden, Janiëlle A. E. M., Bocca, Gianni, Finken, Martijn J. J., Hoorweg‐Nijman, Gera J. G., Jira, Petr E., Leeuwen, Mariëtte, Hokken‐Koelega, Anita C. S.
Published in Clinical endocrinology (Oxford) (01.07.2019)
Published in Clinical endocrinology (Oxford) (01.07.2019)
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Journal Article
SAT-446 No Central Adrenal Insufficiency Found in Adults with Prader-Willi Syndrome Tested by Multiple-Dose Metyrapone Test
Davidse, Kirsten, Rosenberg, Anna, Pellikaan, Karlijn, Donze, Stephany, Hokken-Koelega, Anita, de Graaff-Herder, Laura
Published in Journal of the Endocrine Society (30.04.2019)
Published in Journal of the Endocrine Society (30.04.2019)
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Journal Article
Sleep-related breathing disorders in young adults with Prader-Willi syndrome: a placebo-controlled, cross-over GH trial
Donze, Stephany H, de Weerd, Al W, van den Bossche, Renilde A S, Joosten, Koen F M, Hokken-Koelega, Anita C S
Published in The journal of clinical endocrinology and metabolism (18.04.2019)
Published in The journal of clinical endocrinology and metabolism (18.04.2019)
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Journal Article