Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Layla Damen"'
Autor:
Layla Damen, Stephany H. Donze, Renske J. Kuppens, Nienke E. Bakker, Laura C. G. de Graaff, Janielle A. E. M. van der Velden, Anita C. S. Hokken-Koelega
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Abstract Background In 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 compositio
Externí odkaz:
https://doaj.org/article/e55ec0c0110b4374a3d8a0c6271204f0
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
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
Autor:
Lionne N. Grootjen, Demi J. Trueba-Timmermans, Layla Damen, Eva F. Mahabier, Gerthe F. Kerkhof, Anita C. S. Hokken-Koelega
Publikováno v:
Journal of Clinical Medicine, 11(9):2496. Multidisciplinary Digital Publishing Institute (MDPI)
Journal of Clinical Medicine; Volume 11; Issue 9; Pages: 2496
Journal of Clinical Medicine; Volume 11; Issue 9; Pages: 2496
Long-term effects of growth hormone (GH) treatment in young children with Prader-Willi syndrome (PWS) have never been compared with untreated age-matched controls with PWS, and it is unclear if starting GH in the first year of life is safe and more e
Autor:
Layla Damen, Melitza S. M. Elizabeth, Stephany H. Donze, Sjoerd A. A. van den Berg, Laura C. G. de Graaff, Anita C. S. Hokken-Koelega
Publikováno v:
Journal of Clinical Medicine, 11(5):1280. Multidisciplinary Digital Publishing Institute (MDPI)
Journal of Clinical Medicine; Volume 11; Issue 5; Pages: 1280
Journal of Clinical Medicine; Volume 11; Issue 5; Pages: 1280
In children with Prader–Willi syndrome (PWS), the standard growth hormone (GH) dose often results in high immunoreactive IGF-I levels. These high immunoreactive IGF-I levels lead to concern because their long-term effects are unknown. As a result,
Autor:
Lionne N. Grootjen, Nathalie E. M. Uyl, Inge A. L. P. van Beijsterveldt, Layla Damen, Gerthe F. Kerkhof, Anita C. S. Hokken-Koelega
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 679, p 679 (2022)
Journal of Clinical Medicine, 11(3):679. Multidisciplinary Digital Publishing Institute (MDPI)
Journal of Clinical Medicine; Volume 11; Issue 3; Pages: 679
Journal of Clinical Medicine, 11(3):679. Multidisciplinary Digital Publishing Institute (MDPI)
Journal of Clinical Medicine; Volume 11; Issue 3; Pages: 679
Objective: Prader-Willi syndrome (PWS) is a rare genetic syndrome with a wide spectrum of clinical features in early life. Late diagnoses are still present. We characterized the perinatal and neonatal features of PWS, compared them with those of heal
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
Autor:
Jenny A. Visser, Anita Hokken-Koelega, Alicia F. Juriaans, Layla Damen, Patric J.D. Delhanty, Stephany Hermina Donze, Lionne N. Grootjen, T. Martin Huisman
Publikováno v:
Clinical Endocrinology, 94(5), 774-785. Wiley-Blackwell Publishing Ltd
Clinical Endocrinology
Clinical Endocrinology
Context: Prader-Willi syndrome (PWS) is characterized by hypothalamic dysfunction, hyperphagia and a typical behavioural phenotype, with characteristics of autism spectrum disorder (ASD) like stubbornness, temper tantrums and compulsivity. It has bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65a90bc3b0117447e2cd365c6848ffee
https://pure.eur.nl/en/publications/d011a4ce-e518-46f5-9377-b0ffe6d33d31
https://pure.eur.nl/en/publications/d011a4ce-e518-46f5-9377-b0ffe6d33d31
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