Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Stephany Donze"'
Autor:
Elena G. Bochukova, Katherine Lawler, Sophie Croizier, Julia M. Keogh, Nisha Patel, Garth Strohbehn, Kitty K. Lo, Jack Humphrey, Anita Hokken-Koelega, Layla Damen, Stephany Donze, Sebastien G. Bouret, Vincent Plagnol, I. Sadaf Farooqi
Publikováno v:
Cell Reports, Vol 22, Iss 13, Pp 3401-3408 (2018)
Summary: Transcriptional analysis of brain tissue from people with molecularly defined causes of obesity may highlight disease mechanisms and therapeutic targets. We performed RNA sequencing of hypothalamus from individuals with Prader-Willi syndrome
Externí odkaz:
https://doaj.org/article/4798546d39bd4dc69ff2ac49075ed378
Autor:
Joost P H J Rutges, Gerthe F. Kerkhof, Stephany Donze, Layla Damen, Alicia F Juriaans, Anita C. S. Hokken-Koelega, Lionne N Grootjen
Publikováno v:
European Journal of Endocrinology, 185(1), 47-55. Bioscientifica Ltd
Objective Scoliosis is frequently seen in children with Prader–Willi syndrome (PWS). There is still concern that growth hormone (GH) treatment might increase the risk of onset or progression of scoliosis. Short-term data suggested no adverse effect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::475eb380fda43b14454105acdc3b9283
https://doi.org/10.1530/eje-21-0211
https://doi.org/10.1530/eje-21-0211
Bone mineral density during 3 years of growth hormone in previously GH-treated young adults with PWS
Autor:
Lionne N Grootjen, Stephany Donze, Laura C. G. de Graaff, Anita C. S. Hokken-Koelega, Janiëlle A E M van der Velden, Layla Damen
Publikováno v:
European Journal of Endocrinology, 184, 6, pp. 773-782
European Journal of Endocrinology, 184(6), 773-782. Bioscientifica Ltd
European Journal of Endocrinology, 184, 773-782
European Journal of Endocrinology, 184(6), 773-782. Bioscientifica Ltd
European Journal of Endocrinology, 184, 773-782
Objective In children with Prader–Willi syndrome (PWS), growth hormone (GH) treatment has positive effects on bone mineral density (BMD). Two 1-year studies did not show a difference between GH or placebo on BMD in young adults with PWS. However, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac0b8f981b94afeefb03cd98151bd4a8
https://hdl.handle.net/2066/237282
https://hdl.handle.net/2066/237282
Autor:
Gera Hoorweg-Nijman, Anita C. S. Hokken-Koelega, Martijn J. J. Finken, Mariette van Leeuwen, Stephany Donze, Gianni Bocca, Petr E. Jira, Janiëlle A E M van Alfen-van der Velden, Layla Damen
Publikováno v:
Clinical Endocrinology, 91(1), 118-123. Wiley
Clinical Endocrinology, 91, 118-123
Clinical Endocrinology, 91, 1, pp. 118-123
Clinical Endocrinology, 91(1), 118-123. Wiley-Blackwell Publishing Ltd
Donze, S H, Damen, L, van Alfen-van der Velden, J A E M, Bocca, G, Finken, M J J, Hoorweg-Nijman, G J G, Jira, P E, van Leeuwen, M & Hokken-Koelega, A C S 2019, ' Prevalence of growth hormone (GH) deficiency in previously GH-treated young adults with Prader-Willi syndrome ', Clinical Endocrinology, vol. 91, no. 1, pp. 118-123 . https://doi.org/10.1111/cen.13988
Clinical Endocrinology
Clinical Endocrinology, 91(1), 118-123. Wiley-Blackwell
Clinical Endocrinology, 91, 118-123
Clinical Endocrinology, 91, 1, pp. 118-123
Clinical Endocrinology, 91(1), 118-123. Wiley-Blackwell Publishing Ltd
Donze, S H, Damen, L, van Alfen-van der Velden, J A E M, Bocca, G, Finken, M J J, Hoorweg-Nijman, G J G, Jira, P E, van Leeuwen, M & Hokken-Koelega, A C S 2019, ' Prevalence of growth hormone (GH) deficiency in previously GH-treated young adults with Prader-Willi syndrome ', Clinical Endocrinology, vol. 91, no. 1, pp. 118-123 . https://doi.org/10.1111/cen.13988
Clinical Endocrinology
Clinical Endocrinology, 91(1), 118-123. Wiley-Blackwell
OBJECTIVE: Some features of subjects with Prader-Willi syndrome (PWS) resemble those seen in growth hormone deficiency (GHD). Children with PWS are treated with growth hormone (GH), which has substantially changed their phenotype. Currently, young ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::552835ff4798d883669ccbafe26dea8a
https://hdl.handle.net/2066/204782
https://hdl.handle.net/2066/204782
Publikováno v:
Psychoneuroendocrinology, 132:105335. Elsevier Ltd.
Context: Prader-Willi syndrome (PWS) is characterized by hypothalamic dysfunction. In children with PWS, stress-induced central adrenal insufficiency (CAI) has been described, however, daily life cortisol production may be normal. Hair cortisol conce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d01a3dc30ba4a54a0df7cc05226e7e14
https://pubmed.ncbi.nlm.nih.gov/34225184
https://pubmed.ncbi.nlm.nih.gov/34225184
Autor:
Laura C. G. de Graaff, Layla Damen, Janiëlle A E M van der Velden, Lionne N Grootjen, Stephany Donze, Anita C. S. Hokken-Koelega, Alicia F Juriaans
Publikováno v:
Clinical Endocrinology, 93(4), 439-448. Wiley-Blackwell Publishing Ltd
Context: Growth hormone (GH) has been approved for children with Prader-Willi syndrome (PWS) and significantly improves body composition in adults with PWS. Adults with PWS are predisposed to develop impaired glucose tolerance (IGT) and diabetes mell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69d1c887b46e1e3464514529b214193a
https://pure.eur.nl/en/publications/ebfd9f96-c450-48b4-961c-8c248562017c
https://pure.eur.nl/en/publications/ebfd9f96-c450-48b4-961c-8c248562017c
Autor:
Laura C. G. de Graaff, Layla Damen, Janiëlle A E M van der Velden, Renske Kuppens, Stephany Donze, Nienke Bakker, Anita C. S. Hokken-Koelega
Publikováno v:
Orphanet Journal of Rare Diseases, 15(1):163. BioMed Central Ltd.
Orphanet Journal of Rare Diseases, 15
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Orphanet Journal of Rare Diseases, 15, 1
Orphanet Journal of Rare Diseases, 15
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Orphanet Journal of Rare Diseases, 15, 1
BackgroundIn children with Prader-Willi syndrome (PWS), the benefits of growth hormone treatment are well established. Several one-year studies have shown that growth hormone is also beneficial for adults with PWS, improving body composition. However
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b897aaea0731592c1c3f6ab111901d21
https://pure.eur.nl/en/publications/893f7748-ad8f-4db6-8bb7-6a3c99dc890c
https://pure.eur.nl/en/publications/893f7748-ad8f-4db6-8bb7-6a3c99dc890c
Autor:
Janiëlle A E M van Alfen-van der Velden, Stephany Donze, Nienke Bakker, Anita C. S. Hokken-Koelega, Renske Kuppens
Publikováno v:
Clinical Endocrinology, 88, 6, pp. 806-812
Clinical Endocrinology, 88(6), 806-812. Wiley-Blackwell Publishing Ltd
Clinical Endocrinology, 88, 806-812
Clinical Endocrinology, 88(6), 806-812. Wiley-Blackwell Publishing Ltd
Clinical Endocrinology, 88, 806-812
CONTEXT The prevalence of osteoporosis is increased in adults with Prader-Willi syndrome (PWS). In children with PWS, growth hormone (GH) treatment has beneficial effects on bone mineral density (BMD). BMD might deteriorate after cessation of GH at a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21b928ef2f8e11149ed85eb9a0a412c3
https://doi.org/10.1111/cen.13567
https://doi.org/10.1111/cen.13567
Autor:
Matthew Denniff, Janiëlle A E M van der Velden, Nilesh J. Samani, Wesley J Goedegebuure, Stephany Donze, Anita C. S. Hokken-Koelega, Layla Damen, Veryan Codd
Publikováno v:
The Journal of Clinical Endocrinology and Metabolism
Journal of Clinical Endocrinology and Metabolism, 105, 6, pp. 2053-2059
Journal of Clinical Endocrinology and Metabolism, 105, 2053-2059
Journal of Clinical Endocrinology and Metabolism, 105(6). Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 105, 6, pp. 2053-2059
Journal of Clinical Endocrinology and Metabolism, 105, 2053-2059
Journal of Clinical Endocrinology and Metabolism, 105(6). Endocrine Society
Objective Adults with Prader–Willi syndrome (PWS) are at increased risk of developing age-associated diseases early in life and, like in premature aging syndromes, aging might be accelerated. We investigated leukocyte telomere length (LTL), a marke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::944638e7f23d096775e5b7f8d7d5e1f3
http://europepmc.org/articles/PMC7150612
http://europepmc.org/articles/PMC7150612
Autor:
Anita Hokken-Koelega, Stephany Donze, Robin Peeters, Karlijn Pellikaan, Melitza Elizabeth, Doorn Jaap van, Graaff Laura de, den Berg Sjoerd van
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce49dd069712ca99cdb38f039395cbeb
https://doi.org/10.1530/endoabs.63.gp175
https://doi.org/10.1530/endoabs.63.gp175