Zobrazeno 1 - 10
of 1 123
pro vyhledávání: '"G. De Graaff"'
Autor:
Annelieke R. Müller, Michiel A. J. Luijten, Lotte Haverman, Wendela L. de Ranitz-Greven, Peter Janssens, André B. Rietman, Leontine W. ten Hoopen, Laura C. G. de Graaff, Marie-Claire de Wit, Anna C. Jansen, Tanjala Gipson, Jamie K. Capal, Petrus J. de Vries, Agnies M. van Eeghen
Publikováno v:
BMC Medicine, Vol 21, Iss 1, Pp 1-15 (2023)
Abstract Background Tuberous sclerosis complex (TSC) is a rare and complex genetic disorder, associated with tumor growth in various organ systems, epilepsy, and a range of neuropsychiatric manifestations including intellectual disability. With impro
Externí odkaz:
https://doaj.org/article/3108e33f8bbe45ac9d13900319306ed9
Autor:
Anna G. W. Rosenberg, Ké Mochèl, Lorena M. Hähner, Lara Ruules, Kirsten Davidse, Anja G. Bos-Roubos, Sarah A. van Dijk, M. Carola Zillikens, Walter Taal, Aart J. van der Lely, Laura C. G. de Graaff
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2024)
ContextNeurofibromatosis type 1 (NF1) is a complex system disorder, caused by alterations in RAS pathways. NF1 adults often suffer from chronic and severe fatigue, for which they are frequently referred to Internal Medicine/Endocrinology. Seeking med
Externí odkaz:
https://doaj.org/article/c905e2f7b0944724b698c3897f073159
Autor:
Denise H. van Abswoude, Karlijn Pellikaan, Naomi Nguyen, Anna G. W. Rosenberg, Kirsten Davidse, Franciska M. E. Hoekstra, Ilse M. Rood, Christine Poitou, Graziano Grugni, Charlotte Høybye, Tania P. Markovic, Assumpta Caixàs, Antonino Crinò, Sjoerd A. A. van den Berg, Aart J. van der Lely, Laura C. G. de Graaff
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/4bb7a1911f2d4e0e918bd1cd80546a0c
Autor:
Christine Poitou, Anthony Holland, Charlotte Höybye, Laura C G de Graaff, Sandrine Bottius, Berit Otterlei, Maithé Tauber
Publikováno v:
Endocrine Connections, Vol 12, Iss 1, Pp 1-11 (2022)
Prader–Willi syndrome (PWS), the most common form of syndromic obesity, is a complex neurodevelopmental genetic disorder including obesity with hyperphagia, endocrine and metabolic disorders and also psychiatric disorders. The most frequent endocri
Externí odkaz:
https://doaj.org/article/8dbc53aa9f864b929cd40aede6500eec
Autor:
Denise H. van Abswoude, Karlijn Pellikaan, Naomi Nguyen, Anna G. W. Rosenberg, Kirsten Davidse, Franciska M. E. Hoekstra, Ilse M. Rood, Christine Poitou, Graziano Grugni, Charlotte Høybye, Tania P. Markovic, Assumpta Caixàs, Antonino Crinò, Sjoerd A. A. van den Berg, Aart J. van der Lely, Laura C. G. de Graaff
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundPrader-Willi syndrome (PWS) is a rare, complex, genetic disorder characterized by hyperphagia, hypotonia, delayed psychomotor development, low muscle mass and hypothalamic dysfunction. Adults with PWS often have obesity, hypertension and ty
Externí odkaz:
https://doaj.org/article/b7fe49a89b8d4fd9b087a1e6cebb9573
Autor:
Kirsten Davidse, Anneloes van Staa, Wanda Geilvoet, Judith P van Eck, Karlijn Pellikaan, Janneke Baan, Anita C S Hokken-Koelega, Erica L T van den Akker, Theo Sas, Sabine E Hannema, Aart Jan van der Lely, Laura C G de Graaff
Publikováno v:
Endocrine Connections, Vol 11, Iss 5, Pp 1-9 (2022)
Introduction: Transition from paediatric to adult endocrinology can be challenging for adolescents, their families and healthcare professionals. Previous studies have shown that up to 25% of young adults with endocrine disorders are lost to follow-up
Externí odkaz:
https://doaj.org/article/cd9ce8248c13458b9860b13aea53d851
Autor:
Karlijn Pellikaan, Paula M. H. van Weijen, Anna G. W. Rosenberg, Franciska M. E. Hoekstra, Michiel Vermaak, Peter H. N. Oomen, Aart J. van der Lely, Judith A. A. E. Cuypers, Laura C. G. de Graaff
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
ContextPrader-Willi syndrome (PWS) is a complex rare genetic syndrome. Mortality in patients with PWS is 3% per year. In nearly half of the patients, the cause of death is of cardiopulmonary origin. Prevention, diagnosis and treatment of cardiovascul
Externí odkaz:
https://doaj.org/article/d7dfef0626ef499aa4cd48f7ab092208
Autor:
Annelieke R. Müller, Michiel A. J. Luijten, Lotte Haverman, Wendela L. de Ranitz-Greven, Peter Janssens, André B. Rietman, Leontine W.ten Hoopen, Laura C. G. de Graaff, Marie-Claire de Wit, Anna C. Jansen, Tanjala Gipson, Jamie K. Capal, Petrus J. de Vries, Agnies M. van Eeghen
Publikováno v:
BMC Medicine, Vol 21, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/9fa5f01526794b97b7d76b4251b53f86
Autor:
Lisette van Alewijk, Kirsten Davidse, Karlijn Pellikaan, Judith van Eck, Anita C S Hokken-Koelega, Theo C J Sas, Sabine Hannema, Aart J van der Lely, Laura C G de Graaff
Publikováno v:
Endocrine Connections, Vol 10, Iss 4, Pp 432-446 (2021)
Objective: Adolescents and young adults (AYA) with common endocrine disorders show a high dropout (up to 50%) after the transfer from paediatric to adult endocrinology. Little is known about transition readiness in rare endocrine conditions (rEC). Th
Externí odkaz:
https://doaj.org/article/3257f955ba6d42a2bc3de921cba3e0e2
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