Zobrazeno 1 - 10
of 311
pro vyhledávání: '"A. J. van der Lely"'
Autor:
Eline C. Nijenhuis-Noort, Kirsten A. Berk, Sebastian J. C. M. M. Neggers, Aart J. van der Lely
Publikováno v:
Endocrinology and Metabolism, Vol 39, Iss 1, Pp 83-89 (2024)
This review intends to provide the reader with a practical overview of several (patho)physiological conditions in which knowledge of the interplay between growth hormone (GH), insulin-like growth factor-1 (IGF-1), and insulin is important. This might
Externí odkaz:
https://doaj.org/article/efe13ed3174e4530b0cf5c405d3eb3bf
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:
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:
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:
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:
Mônica R Gadelha, Feng Gu, Marcello D Bronstein, Thierry C Brue, Maria Fleseriu, Ilan Shimon, Aart J van der Lely, Shoba Ravichandran, Albert Kandra, Alberto M Pedroncelli, Annamaria A L Colao
Publikováno v:
Endocrine Connections, Vol 9, Iss 12, Pp 1178-1190 (2020)
Pasireotide, a multireceptor-targeted somatostatin analog with highest affinity for somatostatin receptor subtype (SST) 5, has demonstrated superio r efficacy over the SST2-preferential somatostatin analogs octreotide and lanreotide. The safety profi
Externí odkaz:
https://doaj.org/article/45729ec454b4435ba63f2c136e79dce5
Autor:
Eva C. Coopmans, Sebastiaan W. F. van Meyel, Aart J van der Lely, Sebastian J. C. M. M. Neggers
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 63, Iss 6, Pp 646-652 (2020)
ABSTRACT Advances in combination medical treatment have offer new perspectives for acromegaly patients with persistent disease activity despite receiving the available medical monotherapies. The outcomes of combination medical treatment may reflect b
Externí odkaz:
https://doaj.org/article/111c06bf7f1b4513be1ea6899572159e
Autor:
Anna G. W. Rosenberg, Charlotte M. Wellink, Juan M. Tellez Garcia, Karlijn Pellikaan, Denise H. Van Abswoude, Kirsten Davidse, Laura J. C. M. Van Zutven, Hennie T. Brüggenwirth, James L. Resnick, Aart J. Van der Lely, Laura C. G. De Graaff
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 14, p 4033 (2022)
Prader–Willi syndrome (PWS) is a complex, rare genetic disorder caused by a loss of expression of paternally expressed genes on chromosome 15q11.2-q13. The most common underlying genotypes are paternal deletion (DEL) and maternal uniparental disomy
Externí odkaz:
https://doaj.org/article/a6450b93e6e8469a8c9f7030a0b4ac94
Autor:
Anna G.W. Rosenberg, Wesley Langendoen, Aart J. van der Lely, Jifke F. Veenland, Laura C.G. de Graaff
Publikováno v:
European Journal of Internal Medicine, 106, 154-157. Elsevier